Ginsenosides: changing the basic hallmarks of cancer cells to achieve the purpose of treating breast cancer
In 2021, breast cancer accounted for a substantial proportion of cancer cases and represented the second leading cause of cancer deaths among women worldwide. Although tumor cells originate from normal cells in the human body, they possess distinct biological characteristics resulting from changes i...
Saved in:
Published in | Chinese medicine Vol. 18; no. 1; pp. 1 - 28 |
---|---|
Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
BioMed Central
25.09.2023
BioMed Central Ltd BMC |
Subjects | |
Online Access | Get full text |
ISSN | 1749-8546 1749-8546 |
DOI | 10.1186/s13020-023-00822-9 |
Cover
Abstract | In 2021, breast cancer accounted for a substantial proportion of cancer cases and represented the second leading cause of cancer deaths among women worldwide. Although tumor cells originate from normal cells in the human body, they possess distinct biological characteristics resulting from changes in gene structure and function of cancer cells in contrast with normal cells. These distinguishing features, known as hallmarks of cancer cells, differ from those of normal cells. The hallmarks primarily include high metabolic activity, mitochondrial dysfunction, and resistance to cell death. Current evidence suggests that the fundamental hallmarks of tumor cells affect the tissue structure, function, and metabolism of tumor cells and their internal and external environment. Therefore, these fundamental hallmarks of tumor cells enable tumor cells to proliferate, invade and avoid apoptosis. Modifying these hallmarks of tumor cells represents a new and potentially promising approach to tumor treatment. The key to breast cancer treatment lies in identifying the optimal therapeutic agent with minimal toxicity to normal cells, considering the specific types of tumor cells in patients. Some herbal medicines contain active ingredients which can precisely achieve this purpose. In this review, we introduce Ginsenoside's mechanism and research significance in achieving the therapeutic effect of breast cancer by changing the functional hallmarks of tumor cells, providing a new perspective for the potential application of Ginsenoside as a therapeutic drug for breast cancer. |
---|---|
AbstractList | In 2021, breast cancer accounted for a substantial proportion of cancer cases and represented the second leading cause of cancer deaths among women worldwide. Although tumor cells originate from normal cells in the human body, they possess distinct biological characteristics resulting from changes in gene structure and function of cancer cells in contrast with normal cells. These distinguishing features, known as hallmarks of cancer cells, differ from those of normal cells. The hallmarks primarily include high metabolic activity, mitochondrial dysfunction, and resistance to cell death. Current evidence suggests that the fundamental hallmarks of tumor cells affect the tissue structure, function, and metabolism of tumor cells and their internal and external environment. Therefore, these fundamental hallmarks of tumor cells enable tumor cells to proliferate, invade and avoid apoptosis. Modifying these hallmarks of tumor cells represents a new and potentially promising approach to tumor treatment. The key to breast cancer treatment lies in identifying the optimal therapeutic agent with minimal toxicity to normal cells, considering the specific types of tumor cells in patients. Some herbal medicines contain active ingredients which can precisely achieve this purpose. In this review, we introduce Ginsenoside's mechanism and research significance in achieving the therapeutic effect of breast cancer by changing the functional hallmarks of tumor cells, providing a new perspective for the potential application of Ginsenoside as a therapeutic drug for breast cancer. In 2021, breast cancer accounted for a substantial proportion of cancer cases and represented the second leading cause of cancer deaths among women worldwide. Although tumor cells originate from normal cells in the human body, they possess distinct biological characteristics resulting from changes in gene structure and function of cancer cells in contrast with normal cells. These distinguishing features, known as hallmarks of cancer cells, differ from those of normal cells. The hallmarks primarily include high metabolic activity, mitochondrial dysfunction, and resistance to cell death. Current evidence suggests that the fundamental hallmarks of tumor cells affect the tissue structure, function, and metabolism of tumor cells and their internal and external environment. Therefore, these fundamental hallmarks of tumor cells enable tumor cells to proliferate, invade and avoid apoptosis. Modifying these hallmarks of tumor cells represents a new and potentially promising approach to tumor treatment. The key to breast cancer treatment lies in identifying the optimal therapeutic agent with minimal toxicity to normal cells, considering the specific types of tumor cells in patients. Some herbal medicines contain active ingredients which can precisely achieve this purpose. In this review, we introduce Ginsenoside's mechanism and research significance in achieving the therapeutic effect of breast cancer by changing the functional hallmarks of tumor cells, providing a new perspective for the potential application of Ginsenoside as a therapeutic drug for breast cancer. Keywords: Ginsenoside, Breast cancer, Hallmarks of cancer, Apoptosis, Epithelial-mesenchymal transition, Cell growth Abstract In 2021, breast cancer accounted for a substantial proportion of cancer cases and represented the second leading cause of cancer deaths among women worldwide. Although tumor cells originate from normal cells in the human body, they possess distinct biological characteristics resulting from changes in gene structure and function of cancer cells in contrast with normal cells. These distinguishing features, known as hallmarks of cancer cells, differ from those of normal cells. The hallmarks primarily include high metabolic activity, mitochondrial dysfunction, and resistance to cell death. Current evidence suggests that the fundamental hallmarks of tumor cells affect the tissue structure, function, and metabolism of tumor cells and their internal and external environment. Therefore, these fundamental hallmarks of tumor cells enable tumor cells to proliferate, invade and avoid apoptosis. Modifying these hallmarks of tumor cells represents a new and potentially promising approach to tumor treatment. The key to breast cancer treatment lies in identifying the optimal therapeutic agent with minimal toxicity to normal cells, considering the specific types of tumor cells in patients. Some herbal medicines contain active ingredients which can precisely achieve this purpose. In this review, we introduce Ginsenoside's mechanism and research significance in achieving the therapeutic effect of breast cancer by changing the functional hallmarks of tumor cells, providing a new perspective for the potential application of Ginsenoside as a therapeutic drug for breast cancer. In 2021, breast cancer accounted for a substantial proportion of cancer cases and represented the second leading cause of cancer deaths among women worldwide. Although tumor cells originate from normal cells in the human body, they possess distinct biological characteristics resulting from changes in gene structure and function of cancer cells in contrast with normal cells. These distinguishing features, known as hallmarks of cancer cells, differ from those of normal cells. The hallmarks primarily include high metabolic activity, mitochondrial dysfunction, and resistance to cell death. Current evidence suggests that the fundamental hallmarks of tumor cells affect the tissue structure, function, and metabolism of tumor cells and their internal and external environment. Therefore, these fundamental hallmarks of tumor cells enable tumor cells to proliferate, invade and avoid apoptosis. Modifying these hallmarks of tumor cells represents a new and potentially promising approach to tumor treatment. The key to breast cancer treatment lies in identifying the optimal therapeutic agent with minimal toxicity to normal cells, considering the specific types of tumor cells in patients. Some herbal medicines contain active ingredients which can precisely achieve this purpose. In this review, we introduce Ginsenoside's mechanism and research significance in achieving the therapeutic effect of breast cancer by changing the functional hallmarks of tumor cells, providing a new perspective for the potential application of Ginsenoside as a therapeutic drug for breast cancer.In 2021, breast cancer accounted for a substantial proportion of cancer cases and represented the second leading cause of cancer deaths among women worldwide. Although tumor cells originate from normal cells in the human body, they possess distinct biological characteristics resulting from changes in gene structure and function of cancer cells in contrast with normal cells. These distinguishing features, known as hallmarks of cancer cells, differ from those of normal cells. The hallmarks primarily include high metabolic activity, mitochondrial dysfunction, and resistance to cell death. Current evidence suggests that the fundamental hallmarks of tumor cells affect the tissue structure, function, and metabolism of tumor cells and their internal and external environment. Therefore, these fundamental hallmarks of tumor cells enable tumor cells to proliferate, invade and avoid apoptosis. Modifying these hallmarks of tumor cells represents a new and potentially promising approach to tumor treatment. The key to breast cancer treatment lies in identifying the optimal therapeutic agent with minimal toxicity to normal cells, considering the specific types of tumor cells in patients. Some herbal medicines contain active ingredients which can precisely achieve this purpose. In this review, we introduce Ginsenoside's mechanism and research significance in achieving the therapeutic effect of breast cancer by changing the functional hallmarks of tumor cells, providing a new perspective for the potential application of Ginsenoside as a therapeutic drug for breast cancer. |
ArticleNumber | 125 |
Audience | Academic |
Author | Jiang, Xiao Wang, Xiao-jia Xu, Jun-yao Chen, Ke-yu Wang, Wei Zhang, Huan-ping Jiang, Rui-yuan Fang, Zi-ru Zhu, Jia-yu |
Author_xml | – sequence: 1 givenname: Rui-yuan surname: Jiang fullname: Jiang, Rui-yuan organization: Zhejiang Cancer Hospital, Hangzhou Institute of Medicine (HIM), Chinese Academy of Sciences, Zhejiang Chinese Medical University – sequence: 2 givenname: Zi-ru surname: Fang fullname: Fang, Zi-ru organization: Zhejiang Cancer Hospital, Hangzhou Institute of Medicine (HIM), Chinese Academy of Sciences, Zhejiang Chinese Medical University – sequence: 3 givenname: Huan-ping surname: Zhang fullname: Zhang, Huan-ping organization: Zhejiang Cancer Hospital, Hangzhou Institute of Medicine (HIM), Chinese Academy of Sciences, Wenzhou Medical University – sequence: 4 givenname: Jun-yao surname: Xu fullname: Xu, Jun-yao organization: Zhejiang Cancer Hospital, Hangzhou Institute of Medicine (HIM), Chinese Academy of Sciences – sequence: 5 givenname: Jia-yu surname: Zhu fullname: Zhu, Jia-yu organization: Zhejiang Cancer Hospital, Hangzhou Institute of Medicine (HIM), Chinese Academy of Sciences, Zhejiang Chinese Medical University – sequence: 6 givenname: Ke-yu surname: Chen fullname: Chen, Ke-yu organization: Zhejiang Cancer Hospital, Hangzhou Institute of Medicine (HIM), Chinese Academy of Sciences, Zhejiang Chinese Medical University – sequence: 7 givenname: Wei surname: Wang fullname: Wang, Wei organization: Zhejiang Cancer Hospital, Hangzhou Institute of Medicine (HIM), Chinese Academy of Sciences, Wenzhou Medical University – sequence: 8 givenname: Xiao surname: Jiang fullname: Jiang, Xiao email: jiangx1985@gxtcmu.edu.cn organization: Department of Basic Medical Sciences, Guangxi University of Chinese Medicine – sequence: 9 givenname: Xiao-jia orcidid: 0000-0002-7005-0842 surname: Wang fullname: Wang, Xiao-jia email: wxiaojia0803@163.com organization: Zhejiang Cancer Hospital, Hangzhou Institute of Medicine (HIM), Chinese Academy of Sciences |
BookMark | eNp9ks1u3CAUha0qVfPTvkBXlipV3Ti9gI2hmyqK2jRSpG7aNcL4ekzigSngSHn74plRk4mqiIURnPOBD-e0OHLeYVG8J3BOiOCfI2FAoQLKKgBBaSVfFSekrWUlmpofPZkfF6cx3gI0rGHiTXHM2rzTcDgp7q6si-h8tD3GL6UZtVtZtyrTiGWnozXlqKdprcNdLP1QGu0MhtLgNMUy-VKb0eI9buWbOWx8xEWWAuq0YLo8iWlve1u8HvQU8d3-e1b8_v7t1-WP6ubn1fXlxU1lOOGp6gHrFrTktDc9Y5rVoBkwYkgDAwc-MEJaaBk12BPe8p4PIEzN0TSS1i2ys-J6x-29vlWbYPP1H5TXVm0XfFgpHZI1E6pO5iRFRwQOXS0lk8Abw8xQa8l0PTSZ9XXH2szdGnuDLgU9HUAPd5wd1crfKwINEZK1mfBpTwj-z4wxqbWNS4DaoZ-jooJLSkEQyNIPz6S3fg4uZ5VVy5O1XLSPqpXOf2Dd4PPBZoGqi5ZzzhiFhXX-H1UePa6tyUUabF4_MHx8YhhRT2mMfpqT9S4eCulOaIKPMeDwLw0Caimm2hVT5WKqbTGVzCbxzGRs0gs7X8tOL1vZzhrzOW6F4TGVF1x_AfYn9Uo |
CitedBy_id | crossref_primary_10_3390_nutraceuticals4040027 crossref_primary_10_3390_technologies13010007 crossref_primary_10_3389_fphar_2024_1408993 crossref_primary_10_1080_03639045_2025_2483425 crossref_primary_10_3390_ph17050598 |
Cites_doi | 10.1002/rcm.1862 10.1038/nature15260 10.1016/j.cmet.2022.01.007 10.1016/j.jgr.2017.04.011 10.1007/s12272-021-01345-3 10.1016/j.pharmthera.2017.08.009 10.1200/JCO.2014.59.4358 10.1016/j.gendis.2018.05.001 10.1038/nature14583 10.1089/acm.2011.0591 10.26651/allelo.j/2021-54-1-1350 10.3389/fcvm.2020.00026 10.1111/cpr.13246 10.3390/ijms23179521 10.1016/j.phrs.2019.02.003 10.3346/jkms.2001.16.S.S6 10.3389/fphar.2021.801662 10.1101/cshperspect.a006080 10.1080/19768354.2018.1545696 10.3390/nu12010246 10.1016/j.it.2022.04.010 10.1007/s11101-019-09628-w 10.1016/j.cell.2017.01.002 10.1016/j.jgr.2021.05.004 10.1248/cpb.57.1412 10.1038/nri3191 10.1039/D2GC02639B 10.1002/(SICI)1097-0215(19970529)71:5<787::AID-IJC16>3.0.CO;2-5 10.1016/j.jchromb.2010.06.019 10.1158/2159-8290.CD-15-0563 10.1126/science.1228522 10.7717/peerj.9281 10.1002/jbt.22945 10.5142/jgr.2013.37.124 10.1016/j.patbio.2012.05.012 10.1007/s10549-012-2289-9 10.3390/ijms221910458 10.1093/carcin/bgv123 10.1016/j.tranon.2020.100773 10.1039/C8RA04879G 10.1136/heartjnl-2017-312103 10.3389/fcell.2022.1068720 10.1189/jlb.1107774 10.1155/2020/8886955 10.1142/S0192415X22500720 10.3389/fcimb.2022.853981 10.3390/ph15050626 10.1038/s41556-018-0201-5 10.2144/fsoa-2020-0076 10.1016/j.bbrc.2021.10.067 10.1126/sciadv.abj1262 10.1186/s12951-022-01623-2 10.1093/annonc/mdz173 10.1080/13813450801900645 10.1016/j.cell.2011.02.013 10.1016/j.jgr.2021.11.004 10.3892/mmr.2012.981 10.1016/j.jare.2022.09.007 10.1001/jamanetworkopen.2022.54677 10.1088/1361-6528/abe1f0 10.1016/j.intimp.2020.106535 10.1007/s11655-007-9002-6 10.1016/j.jep.2008.12.012 10.1002/bies.201000016 10.3390/cancers15041335 10.3390/pr9081344 10.2147/IJN.S221328 10.3322/caac.21708 10.1016/j.tox.2019.02.010 10.1002/ptr.6636 10.1016/j.cca.2019.01.011 10.1007/s12272-019-01115-2 10.1042/BST20110609 10.1007/s12094-019-02187-8 10.1148/radiol.2016150719 10.1038/srep33709 10.1016/j.bbrc.2018.03.174 10.3390/medicines6010017 10.1586/14737159.2015.1084229 10.1016/j.coi.2014.01.004 10.1016/j.jchromb.2004.11.036 10.1371/journal.pone.0240533 10.3322/caac.21397 10.1016/j.tibs.2015.12.001 10.2174/1568026619666191018100848 10.2174/1874467214666210120153348 10.1016/j.tem.2004.05.011 10.1002/cpdd.877 10.3390/ijms23169077 10.1038/s41571-021-00588-9 10.3390/jcm9010084 10.1155/2016/5738694 10.1172/JCI45014 10.1038/nrc.2015.2 10.3109/13880209.2015.1101142 10.1038/s41571-020-0341-y 10.1142/S0192415X18500702 10.3390/biom11010118 10.1016/j.bbcan.2017.06.006 10.1039/C8FO01122B 10.1158/2159-8290.CD-21-1059 10.1016/j.jep.2014.04.051 10.1007/s11684-020-0793-6 10.1001/jamaoncol.2018.7147 10.1038/nrclinonc.2016.144 10.1038/s42255-020-00317-z 10.1016/j.semcancer.2019.12.018 10.1016/j.biopha.2020.109891 10.3390/ph14070633 10.3892/ijmm.2013.1519 10.1016/j.jgr.2019.02.004 10.18632/aging.203131 10.18632/oncotarget.12059 10.1007/s12195-017-0485-8 10.3390/ijms23042288 10.1016/j.cell.2009.08.007 10.3390/cancers14030474 10.3389/fimmu.2020.00940 10.1016/j.jgr.2017.05.003 10.1016/j.bcp.2022.115101 10.1007/s12272-022-01377-3 10.1002/rcm.9083 10.1016/j.biopha.2017.02.038 10.1038/nrc3603 10.1097/CM9.0000000000000498 10.1016/j.jff.2019.04.019 10.1016/j.tig.2021.06.014 10.1039/C5AY01365H 10.18632/oncotarget.9059 10.1016/j.prp.2022.153956 10.1128/MCB.20.21.8069-8083.2000 10.3390/biom10040528 10.3390/ijms19113466 10.1016/j.jgr.2018.03.004 10.1186/1749-8546-5-19 10.1016/j.fct.2011.06.020 10.1016/j.semcancer.2015.02.006 10.3724/abbs.2022039 10.3892/or.2017.5652 10.1016/j.jgr.2018.05.004 10.1002/cam4.2474 10.1371/journal.pone.0002697 10.5142/jgr.2012.36.1.102 10.1142/S0192415X19500848 10.1093/carcin/bgt480 10.1039/C5TB02305J 10.3389/fphar.2021.797634 10.3109/00498254.2014.929192 10.1038/nrclinonc.2015.61 10.1016/j.semcancer.2020.08.009 10.1016/S0092-8674(00)81683-9 10.1002/ptr.2384 10.1016/S0140-6736(20)30165-3 10.3390/cancers13081892 10.1002/bmc.3037 10.1016/j.apjtm.2016.01.010 10.2217/nnm-2021-0329 10.1007/s12272-020-01265-8 10.3390/cancers10040101 |
ContentType | Journal Article |
Copyright | The Author(s) 2023 COPYRIGHT 2023 BioMed Central Ltd. 2023. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2023. International Society for Chinese Medicine and BioMed Central Ltd. International Society for Chinese Medicine and BioMed Central Ltd. 2023 |
Copyright_xml | – notice: The Author(s) 2023 – notice: COPYRIGHT 2023 BioMed Central Ltd. – notice: 2023. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. – notice: 2023. International Society for Chinese Medicine and BioMed Central Ltd. – notice: International Society for Chinese Medicine and BioMed Central Ltd. 2023 |
DBID | C6C AAYXX CITATION 3V. 7T5 7TM 7X7 7XB 8FD 8FI 8FJ 8FK ABUWG AFKRA AZQEC BENPR CCPQU DWQXO FR3 FYUFA GHDGH H94 K9. M0S P64 PHGZM PHGZT PIMPY PKEHL PQEST PQQKQ PQUKI RC3 7X8 5PM DOA |
DOI | 10.1186/s13020-023-00822-9 |
DatabaseName | Springer Nature OA Free Journals CrossRef ProQuest Central (Corporate) Immunology Abstracts Nucleic Acids Abstracts ProQuest Health & Medical Collection ProQuest Central (purchase pre-March 2016) Technology Research Database Hospital Premium Collection Hospital Premium Collection (Alumni Edition) ProQuest Central (Alumni) (purchase pre-March 2016) ProQuest Central (Alumni) ProQuest Central UK/Ireland ProQuest Central Essentials AUTh Library subscriptions: ProQuest Central ProQuest One ProQuest Central Korea Engineering Research Database Health Research Premium Collection Health Research Premium Collection (Alumni) AIDS and Cancer Research Abstracts ProQuest Health & Medical Complete (Alumni) Health & Medical Collection (Alumni Edition) Biotechnology and BioEngineering Abstracts ProQuest Central Premium ProQuest One Academic (New) ProQuest Publicly Available Content Database ProQuest One Academic Middle East (New) ProQuest One Academic Eastern Edition (DO NOT USE) ProQuest One Academic ProQuest One Academic UKI Edition Genetics Abstracts MEDLINE - Academic PubMed Central (Full Participant titles) DOAJ Directory of Open Access Journals |
DatabaseTitle | CrossRef Publicly Available Content Database Technology Research Database ProQuest One Academic Middle East (New) ProQuest Central Essentials Nucleic Acids Abstracts ProQuest Health & Medical Complete (Alumni) ProQuest Central (Alumni Edition) ProQuest One Community College ProQuest Central Genetics Abstracts Health Research Premium Collection Health and Medicine Complete (Alumni Edition) ProQuest Central Korea AIDS and Cancer Research Abstracts ProQuest Central (New) ProQuest One Academic Eastern Edition ProQuest Hospital Collection Health Research Premium Collection (Alumni) ProQuest Hospital Collection (Alumni) Biotechnology and BioEngineering Abstracts ProQuest Health & Medical Complete ProQuest One Academic UKI Edition Immunology Abstracts Engineering Research Database ProQuest One Academic ProQuest One Academic (New) ProQuest Central (Alumni) MEDLINE - Academic |
DatabaseTitleList | CrossRef MEDLINE - Academic Publicly Available Content Database |
Database_xml | – sequence: 1 dbid: C6C name: Springer Nature OA Free Journals url: http://www.springeropen.com/ sourceTypes: Publisher – sequence: 2 dbid: DOA name: DOAJ Directory of Open Access Journals url: https://www.doaj.org/ sourceTypes: Open Website – sequence: 3 dbid: BENPR name: ProQuest Central url: http://www.proquest.com/pqcentral?accountid=15518 sourceTypes: Aggregation Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 1749-8546 |
EndPage | 28 |
ExternalDocumentID | oai_doaj_org_article_b91188b18efb49939065c3cf4a93a4f5 PMC10518937 A766633200 10_1186_s13020_023_00822_9 |
GeographicLocations | United States--US |
GeographicLocations_xml | – name: United States--US |
GrantInformation_xml | – fundername: Zhejiang Traditional Chinese Medicine Administration grantid: 2015zz004 funderid: http://dx.doi.org/10.13039/501100012175 – fundername: ; grantid: 2015zz004 |
GroupedDBID | --- 0R~ 29B 2WC 53G 5GY 5VS 6J9 6PF 7X7 8FI 8FJ AAFWJ AAJSJ AASML AAWTL ABDBF ABUWG ACGFO ACGFS ACIHN ACPRK ACUHS ADBBV ADUKV AEAQA AENEX AFKRA AFPKN AFRAH AHBYD AHMBA AHSBF AHYZX ALMA_UNASSIGNED_HOLDINGS AMKLP AMTXH AOIJS BAPOH BAWUL BCNDV BENPR BFQNJ BMC BPHCQ BVXVI C6C CCPQU CS3 DIK DU5 E3Z EBD EBLON EBS ESX F5P FYUFA GROUPED_DOAJ GS5 GX1 HMCUK HYE IAO IHR IHW ITC OK1 OVT P2P PGMZT PHGZM PHGZT PIMPY PQQKQ PROAC PUEGO RBZ RNS ROL RPM RSV SMD SOJ TUS UKHRP UNMZH WOQ WOW ~8M AAYXX ALIPV CITATION PMFND 3V. 7T5 7TM 7XB 8FD 8FK AZQEC DWQXO FR3 H94 K9. P64 PKEHL PQEST PQUKI RC3 7X8 5PM |
ID | FETCH-LOGICAL-c616t-d0e470a962dcd33a340a3031c150f606f31170732ced1676d6f08c46ec59247e3 |
IEDL.DBID | 7X7 |
ISSN | 1749-8546 |
IngestDate | Wed Aug 27 01:30:00 EDT 2025 Thu Aug 21 18:36:07 EDT 2025 Thu Sep 04 18:05:03 EDT 2025 Sat Sep 20 14:21:48 EDT 2025 Tue Jun 17 22:21:40 EDT 2025 Tue Jun 10 21:17:31 EDT 2025 Thu May 22 21:20:39 EDT 2025 Tue Jul 01 01:00:04 EDT 2025 Thu Apr 24 22:53:34 EDT 2025 Sat Sep 06 07:29:34 EDT 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 1 |
Keywords | Epithelial-mesenchymal transition Hallmarks of cancer Cell growth Breast cancer Ginsenoside Apoptosis |
Language | English |
License | Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c616t-d0e470a962dcd33a340a3031c150f606f31170732ced1676d6f08c46ec59247e3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Review-3 content type line 23 |
ORCID | 0000-0002-7005-0842 |
OpenAccessLink | https://www.proquest.com/docview/2877497687?pq-origsite=%requestingapplication% |
PMID | 37749560 |
PQID | 2877497687 |
PQPubID | 54985 |
PageCount | 28 |
ParticipantIDs | doaj_primary_oai_doaj_org_article_b91188b18efb49939065c3cf4a93a4f5 pubmedcentral_primary_oai_pubmedcentral_nih_gov_10518937 proquest_miscellaneous_2869220810 proquest_journals_2877497687 gale_infotracmisc_A766633200 gale_infotracacademiconefile_A766633200 gale_healthsolutions_A766633200 crossref_primary_10_1186_s13020_023_00822_9 crossref_citationtrail_10_1186_s13020_023_00822_9 springer_journals_10_1186_s13020_023_00822_9 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2023-09-25 |
PublicationDateYYYYMMDD | 2023-09-25 |
PublicationDate_xml | – month: 09 year: 2023 text: 2023-09-25 day: 25 |
PublicationDecade | 2020 |
PublicationPlace | London |
PublicationPlace_xml | – name: London |
PublicationTitle | Chinese medicine |
PublicationTitleAbbrev | Chin Med |
PublicationYear | 2023 |
Publisher | BioMed Central BioMed Central Ltd BMC |
Publisher_xml | – name: BioMed Central – name: BioMed Central Ltd – name: BMC |
References | D Mayer (822_CR80) 2008; 114 SH Bae (822_CR42) 2014; 44 P Sarvari (822_CR107) 2022; 23 ZL Wang (822_CR31) 2021; 10 S Kim (822_CR30) 2021; 9 Y Jin (822_CR72) 2021; 22 Y Hong (822_CR63) 2019; 418 X Luo (822_CR149) 2021; 13 CN Baxevanis (822_CR140) 2021; 72 TN Seyfried (822_CR124) 2014; 35 J Lee (822_CR34) 2009; 122 T Qian (822_CR39) 2005; 816 P Jiang (822_CR32) 2014; 28 T Qian (822_CR36) 2010; 5 P Lu (822_CR50) 2008; 14 N-H Lee (822_CR45) 2012; 18 E Aksamitiene (822_CR85) 2012; 40 M Singh (822_CR152) 2018; 182 TK Yun (822_CR17) 2001; 16 DR Green (822_CR56) 2015; 7 J-X Miao (822_CR166) 2019; 132 H Mohammed (822_CR87) 2015; 523 SC Linn (822_CR23) 1997; 71 S-Y Kim (822_CR127) 2019; 42 MG Fradley (822_CR162) 2023; 6 V Zanuso (822_CR7) 2020; 6 SK Seo (822_CR44) 2014; 154 DTN Huynh (822_CR70) 2021; 13 B Zhou (822_CR51) 2016; 280 PLT My (822_CR79) 2020; 56 Y Zhu (822_CR147) 2022 RL Kan (822_CR106) 2022; 38 Y Zhang (822_CR10) 2019; 19 S Ren (822_CR46) 2022; 24 M Nakhjavani (822_CR177) 2019; 6 V Changizi (822_CR59) 2021; 46 MWL Teng (822_CR135) 2008; 84 M Pickup (822_CR84) 2013; 13 I Elia (822_CR125) 2021; 3 M Li (822_CR16) 2021; 12 A Kang (822_CR33) 2015; 7 H Beug (822_CR100) 2009; 138 B Zhang (822_CR130) 2022; 202 H Pang (822_CR40) 2001; 36 X-J Chen (822_CR48) 2016; 2016 H Greenlee (822_CR6) 2017; 67 Y Jin (822_CR174) 2020; 43 NR Maimela (822_CR139) 2019; 17 C Hu (822_CR119) 2021; 45 DJ Propper (822_CR145) 2022; 19 Y Zeng (822_CR67) 2020; 47 SS Menon (822_CR81) 2019; 491 Y Jin (822_CR71) 2022; 45 J Zhang (822_CR137) 2022; 43 L Ruan (822_CR15) 2022; 236 J Doherty (822_CR73) 2018; 20 D Hanahan (822_CR20) 2011; 144 D Zhang (822_CR121) 2021; 15 Y Zhan (822_CR26) 2021; 54 P Wang (822_CR49) 2020; 8 G Liu (822_CR167) 2022; 2022 RI Teleanu (822_CR93) 2020; 9 Y Li (822_CR77) 2021; 583 J Hou (822_CR103) 2020; 34 GS Wang (822_CR2) 2012; 6 M Younas (822_CR25) 2018; 8 M Hao (822_CR35) 2008; 3 BA Carneiro (822_CR55) 2020; 17 DA Lawson (822_CR96) 2015; 526 Z Wu (822_CR122) 2020; 22 D Mittal (822_CR141) 2014; 27 D Hanahan (822_CR12) 2022; 12 G Liu (822_CR168) 2021; 21 JH Cho (822_CR91) 2016; 7 A Tubbs (822_CR104) 2017; 168 LM Spring (822_CR88) 2020; 395 J Xia (822_CR148) 2022; 8 F Queiroga (822_CR172) 2023; 15 RL Siegel (822_CR1) 2022; 72 F Cardoso (822_CR5) 2019; 30 YH Guo (822_CR18) 2019; 19 WP Roos (822_CR54) 2016; 16 Y Feng (822_CR97) 2018; 5 H Kim (822_CR114) 2021; 11 D Yang (822_CR38) 2021; 35 K Barzaman (822_CR4) 2020; 84 P Wang (822_CR158) 2016; 6 ML Thomas (822_CR105) 2018; 10 L Ma (822_CR69) 2020; 103 MV Liberti (822_CR123) 2016; 41 L Tarantini (822_CR165) 2006; 13 L Yuan (822_CR9) 2021; 12 S Goossens (822_CR155) 2017; 1868 Q-G Gao (822_CR90) 2019; 43 M Nakhjavani (822_CR102) 2021; 14 D Ribatti (822_CR154) 2020; 13 RD York (822_CR86) 2000; 20 E Zhang (822_CR94) 2017; 38 D Hanahan (822_CR19) 2000; 100 YZ Xiang (822_CR27) 2008; 22 Y Chung (822_CR75) 2018; 22 L Dai (822_CR178) 2016; 4 J Hong (822_CR120) 2022; 46 MA Postow (822_CR146) 2015; 33 A Del Prete (822_CR136) 2022; 10 H Dillekas (822_CR151) 2019; 8 PA Henriksen (822_CR164) 2018; 104 H-G Kim (822_CR43) 2011; 49 J Xia (822_CR131) 2022; 20 M Yu (822_CR153) 2013; 339 JH Song (822_CR156) 2020; 15 Z Su (822_CR92) 2015; 14 H Gao (822_CR132) 2020; 124 D-H Kim (822_CR175) 2018; 42 Y Chu (822_CR65) 2020; 2020 A Ribas (822_CR134) 2015; 5 MA Feitelson (822_CR82) 2015; 35 Y Liu (822_CR61) 2020; 12 A Mohammadalipour (822_CR99) 2017; 10 SA Lee (822_CR47) 2012; 36 Z Yuan (822_CR58) 2017; 89 D Wang (822_CR142) 2015; 36 H Richly (822_CR110) 2010; 32 Z Luo (822_CR78) 2021; 32 H Masuda (822_CR83) 2012; 136 IW Kim (822_CR28) 2013; 37 TG Odle (822_CR161) 2014; 85 Y Zhang (822_CR95) 2016; 9 H-M Oh (822_CR57) 2022; 23 Z Chen (822_CR176) 2022; 12 NN Pavlova (822_CR126) 2022; 34 D Cardinale (822_CR163) 2020; 7 S Adams (822_CR143) 2019; 5 B Peng (822_CR160) 2019; 142 SJ Skuli (822_CR128) 2022; 15 YJ Kim (822_CR66) 2019; 14 CW Yun (822_CR74) 2018; 19 AM Jankowska (822_CR108) 2015; 15 S Liu (822_CR64) 2022; 36 K Zhang (822_CR159) 2016; 54 C Li (822_CR170) 2021; 16 J Hou (822_CR169) 2022; 55 F Nakasuka (822_CR109) 2020; 47 Q Zhao (822_CR41) 2010; 878 M Mohme (822_CR133) 2017; 14 Y Li (822_CR171) 2016; 7 G Dontu (822_CR21) 2004; 15 D Jeong (822_CR115) 2019; 47 NH Tung (822_CR29) 2009; 57 LJ Brown (822_CR111) 2022; 14 C Hong (822_CR150) 2020; 12 S Ravi (822_CR13) 2022; 14 D Molnar-Stanciu (822_CR14) 2012; 60 Z Duan (822_CR68) 2018; 499 K Peng (822_CR89) 2022; 54 X Li (822_CR52) 2015; 37 YS Wang (822_CR157) 2020; 10 F Hashemi (822_CR24) 2021; 14 F Lei (822_CR173) 2010; 35 Y Hong (822_CR62) 2019; 57 J Oh (822_CR101) 2019; 43 J-S Choi (822_CR53) 2013; 32 M Ebrahimi (822_CR22) 2010; 15 H Lee (822_CR118) 2018; 42 A Labani-Motlagh (822_CR138) 2020; 11 N Takebe (822_CR98) 2015; 12 Y Liu (822_CR60) 2018; 9 H Jeon (822_CR76) 2021; 44 G Sher (822_CR112) 2022; 83 J Ham (822_CR113) 2019; 43 J Ham (822_CR117) 2018; 46 D Micic (822_CR129) 2011; 10 BD Lehmann (822_CR3) 2011; 121 KH Lau (822_CR8) 2022; 23 YA Fouad (822_CR11) 2017; 7 K Li (822_CR37) 2005; 19 NP Restifo (822_CR144) 2012; 12 JE Park (822_CR116) 2022; 50 |
References_xml | – volume: 7 start-page: 1016 issue: 5 year: 2017 ident: 822_CR11 publication-title: Am J Cancer Res – volume: 19 start-page: 813 issue: 6 year: 2005 ident: 822_CR37 publication-title: Rapid Commun Mass Spectrom: RCM doi: 10.1002/rcm.1862 – volume: 17 start-page: 1 year: 2019 ident: 822_CR139 publication-title: Biotechnol J – volume: 526 start-page: 131 issue: 7571 year: 2015 ident: 822_CR96 publication-title: Nature doi: 10.1038/nature15260 – volume: 34 start-page: 355 issue: 3 year: 2022 ident: 822_CR126 publication-title: Cell Metab doi: 10.1016/j.cmet.2022.01.007 – volume: 42 start-page: 255 issue: 3 year: 2018 ident: 822_CR175 publication-title: J Ginseng Res doi: 10.1016/j.jgr.2017.04.011 – volume: 44 start-page: 702 issue: 7 year: 2021 ident: 822_CR76 publication-title: Arch Pharm Res doi: 10.1007/s12272-021-01345-3 – volume: 21 start-page: 1 issue: 5 year: 2021 ident: 822_CR168 publication-title: Exp Ther Med – volume: 182 start-page: 80 year: 2018 ident: 822_CR152 publication-title: Pharmacol Ther doi: 10.1016/j.pharmthera.2017.08.009 – volume: 33 start-page: 1974 issue: 17 year: 2015 ident: 822_CR146 publication-title: J Clin Oncol doi: 10.1200/JCO.2014.59.4358 – volume: 5 start-page: 77 issue: 2 year: 2018 ident: 822_CR97 publication-title: Genes Dis doi: 10.1016/j.gendis.2018.05.001 – volume: 523 start-page: 313 issue: 7560 year: 2015 ident: 822_CR87 publication-title: Nature doi: 10.1038/nature14583 – volume: 35 start-page: 2221 issue: 17 year: 2010 ident: 822_CR173 publication-title: Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi =China J Chin Mater Med – volume: 18 start-page: 1061 issue: 11 year: 2012 ident: 822_CR45 publication-title: J Altern Complement Med doi: 10.1089/acm.2011.0591 – volume: 54 start-page: 81 issue: 1 year: 2021 ident: 822_CR26 publication-title: Allelopathy J doi: 10.26651/allelo.j/2021-54-1-1350 – volume: 7 start-page: 26 year: 2020 ident: 822_CR163 publication-title: Front Cardiovasc Med doi: 10.3389/fcvm.2020.00026 – volume: 55 start-page: e13246 issue: 6 year: 2022 ident: 822_CR169 publication-title: Cell Prolif doi: 10.1111/cpr.13246 – volume: 23 start-page: 9521 issue: 17 year: 2022 ident: 822_CR107 publication-title: Int J Mol Sci doi: 10.3390/ijms23179521 – volume: 142 start-page: 1 year: 2019 ident: 822_CR160 publication-title: Pharmacol Res doi: 10.1016/j.phrs.2019.02.003 – volume: 16 start-page: S6 issue: Suppl year: 2001 ident: 822_CR17 publication-title: J Korean Med Sci doi: 10.3346/jkms.2001.16.S.S6 – volume: 12 start-page: 801662 year: 2021 ident: 822_CR9 publication-title: Front Pharmacol doi: 10.3389/fphar.2021.801662 – volume: 7 start-page: a006080 issue: 12 year: 2015 ident: 822_CR56 publication-title: Cold Spring Harbor Perspect Biol doi: 10.1101/cshperspect.a006080 – volume: 22 start-page: 382 issue: 6 year: 2018 ident: 822_CR75 publication-title: Anim Cells Syst doi: 10.1080/19768354.2018.1545696 – volume: 12 start-page: 246 issue: 1 year: 2020 ident: 822_CR61 publication-title: Nutrients doi: 10.3390/nu12010246 – volume: 47 start-page: 1407 issue: 10 year: 2020 ident: 822_CR109 publication-title: Cancer Chemother – volume: 43 start-page: 523 issue: 7 year: 2022 ident: 822_CR137 publication-title: Trends Immunol doi: 10.1016/j.it.2022.04.010 – volume: 12 start-page: 129 issue: 1 year: 2020 ident: 822_CR150 publication-title: Nanomicro Lett – volume: 19 start-page: 1179 issue: 5 year: 2019 ident: 822_CR10 publication-title: Phytochem Rev doi: 10.1007/s11101-019-09628-w – volume: 168 start-page: 644 issue: 4 year: 2017 ident: 822_CR104 publication-title: Cell doi: 10.1016/j.cell.2017.01.002 – volume: 45 start-page: 734 issue: 6 year: 2021 ident: 822_CR119 publication-title: J Ginseng Res doi: 10.1016/j.jgr.2021.05.004 – volume: 57 start-page: 1412 issue: 12 year: 2009 ident: 822_CR29 publication-title: Chem Pharm Bull doi: 10.1248/cpb.57.1412 – volume: 12 start-page: 269 issue: 4 year: 2012 ident: 822_CR144 publication-title: Nat Rev Immunol doi: 10.1038/nri3191 – volume: 24 start-page: 8302 issue: 21 year: 2022 ident: 822_CR46 publication-title: Green Chem doi: 10.1039/D2GC02639B – volume: 14 start-page: e24803 issue: 5 year: 2022 ident: 822_CR13 publication-title: Cureus – volume: 71 start-page: 787 issue: 5 year: 1997 ident: 822_CR23 publication-title: Int J Cancer doi: 10.1002/(SICI)1097-0215(19970529)71:5<787::AID-IJC16>3.0.CO;2-5 – volume: 878 start-page: 2266 issue: 24 year: 2010 ident: 822_CR41 publication-title: J Chromatogr B-Anal Technol Biomed Life Sci doi: 10.1016/j.jchromb.2010.06.019 – volume: 5 start-page: 915 issue: 9 year: 2015 ident: 822_CR134 publication-title: Cancer Discov doi: 10.1158/2159-8290.CD-15-0563 – volume: 339 start-page: 580 issue: 6119 year: 2013 ident: 822_CR153 publication-title: Science doi: 10.1126/science.1228522 – volume: 8 start-page: e9281 year: 2020 ident: 822_CR49 publication-title: PeerJ doi: 10.7717/peerj.9281 – volume: 36 start-page: e22945 issue: 1 year: 2022 ident: 822_CR64 publication-title: J Biochem Mol Toxicol doi: 10.1002/jbt.22945 – volume: 37 start-page: 124 issue: 1 year: 2013 ident: 822_CR28 publication-title: J Ginseng Res doi: 10.5142/jgr.2013.37.124 – volume: 60 start-page: 254 issue: 4 year: 2012 ident: 822_CR14 publication-title: Pathol Biol doi: 10.1016/j.patbio.2012.05.012 – volume: 136 start-page: 331 issue: 2 year: 2012 ident: 822_CR83 publication-title: Breast Cancer Res Treat doi: 10.1007/s10549-012-2289-9 – volume: 22 start-page: 10458 issue: 19 year: 2021 ident: 822_CR72 publication-title: Int J Mol Sci doi: 10.3390/ijms221910458 – volume: 36 start-page: 1085 issue: 10 year: 2015 ident: 822_CR142 publication-title: Carcinogenesis doi: 10.1093/carcin/bgv123 – volume: 13 start-page: 100773 issue: 6 year: 2020 ident: 822_CR154 publication-title: Transl Oncol doi: 10.1016/j.tranon.2020.100773 – volume: 8 start-page: 29714 issue: 52 year: 2018 ident: 822_CR25 publication-title: RSC Adv doi: 10.1039/C8RA04879G – volume: 104 start-page: 971 issue: 12 year: 2018 ident: 822_CR164 publication-title: Heart doi: 10.1136/heartjnl-2017-312103 – volume: 10 start-page: 1068720 year: 2022 ident: 822_CR136 publication-title: Front Cell Dev Biol doi: 10.3389/fcell.2022.1068720 – volume: 84 start-page: 988 issue: 4 year: 2008 ident: 822_CR135 publication-title: J Leukoc Biol doi: 10.1189/jlb.1107774 – volume: 46 start-page: 291 issue: 4 year: 2021 ident: 822_CR59 publication-title: Iran J Med Sci – volume: 2020 start-page: 8886955 year: 2020 ident: 822_CR65 publication-title: Evid Based Compl Alternat Med doi: 10.1155/2020/8886955 – volume: 50 start-page: 1703 issue: 6 year: 2022 ident: 822_CR116 publication-title: Am J Chin Med doi: 10.1142/S0192415X22500720 – volume: 12 start-page: 853981 year: 2022 ident: 822_CR176 publication-title: Front Cell Infect Microbiol doi: 10.3389/fcimb.2022.853981 – volume: 15 start-page: 626 issue: 5 year: 2022 ident: 822_CR128 publication-title: Pharmaceuticals doi: 10.3390/ph15050626 – volume: 20 start-page: 1110 issue: 10 year: 2018 ident: 822_CR73 publication-title: Nat Cell Biol doi: 10.1038/s41556-018-0201-5 – volume: 6 start-page: FSO617 issue: 9 year: 2020 ident: 822_CR7 publication-title: Future Sci OA doi: 10.2144/fsoa-2020-0076 – volume: 583 start-page: 184 year: 2021 ident: 822_CR77 publication-title: Biochem Biophys Res Commun doi: 10.1016/j.bbrc.2021.10.067 – volume: 8 start-page: eabj1262 issue: 6 year: 2022 ident: 822_CR148 publication-title: Sci Adv doi: 10.1126/sciadv.abj1262 – volume: 20 start-page: 414 issue: 1 year: 2022 ident: 822_CR131 publication-title: J Nanobiotechnology doi: 10.1186/s12951-022-01623-2 – volume: 30 start-page: 1194 issue: 8 year: 2019 ident: 822_CR5 publication-title: Ann Oncol doi: 10.1093/annonc/mdz173 – volume: 114 start-page: 38 issue: 1 year: 2008 ident: 822_CR80 publication-title: Arch Physiol Biochem doi: 10.1080/13813450801900645 – volume: 13 start-page: 54S issue: 5 Suppl 1 year: 2006 ident: 822_CR165 publication-title: G Ital Cardiol – volume: 144 start-page: 646 issue: 5 year: 2011 ident: 822_CR20 publication-title: Cell doi: 10.1016/j.cell.2011.02.013 – volume: 46 start-page: 481 issue: 3 year: 2022 ident: 822_CR120 publication-title: J Ginseng Res doi: 10.1016/j.jgr.2021.11.004 – volume: 6 start-page: 779 issue: 4 year: 2012 ident: 822_CR2 publication-title: Mol Med Rep doi: 10.3892/mmr.2012.981 – year: 2022 ident: 822_CR147 publication-title: J Adv Res doi: 10.1016/j.jare.2022.09.007 – volume: 6 start-page: e2254677 issue: 2 year: 2023 ident: 822_CR162 publication-title: JAMA Netw Open doi: 10.1001/jamanetworkopen.2022.54677 – volume: 32 start-page: 195103 issue: 19 year: 2021 ident: 822_CR78 publication-title: Nanotechnology doi: 10.1088/1361-6528/abe1f0 – volume: 84 start-page: 106535 year: 2020 ident: 822_CR4 publication-title: Int Immunopharmacol doi: 10.1016/j.intimp.2020.106535 – volume: 14 start-page: 33 issue: 1 year: 2008 ident: 822_CR50 publication-title: Chin J Integr Med doi: 10.1007/s11655-007-9002-6 – volume: 122 start-page: 143 issue: 1 year: 2009 ident: 822_CR34 publication-title: J Ethnopharmacol doi: 10.1016/j.jep.2008.12.012 – volume: 32 start-page: 669 issue: 8 year: 2010 ident: 822_CR110 publication-title: BioEssays doi: 10.1002/bies.201000016 – volume: 15 start-page: 1335 issue: 4 year: 2023 ident: 822_CR172 publication-title: Cancers doi: 10.3390/cancers15041335 – volume: 9 start-page: 1344 issue: 8 year: 2021 ident: 822_CR30 publication-title: Processes doi: 10.3390/pr9081344 – volume: 14 start-page: 8195 year: 2019 ident: 822_CR66 publication-title: Int J Nanomed doi: 10.2147/IJN.S221328 – volume: 72 start-page: 7 issue: 1 year: 2022 ident: 822_CR1 publication-title: CA Cancer J Clin doi: 10.3322/caac.21708 – volume: 418 start-page: 22 year: 2019 ident: 822_CR63 publication-title: Toxicology doi: 10.1016/j.tox.2019.02.010 – volume: 34 start-page: 1659 issue: 7 year: 2020 ident: 822_CR103 publication-title: Phytother Res doi: 10.1002/ptr.6636 – volume: 491 start-page: 39 year: 2019 ident: 822_CR81 publication-title: Clin Chim Acta doi: 10.1016/j.cca.2019.01.011 – volume: 42 start-page: 140 issue: 2 year: 2019 ident: 822_CR127 publication-title: Arch Pharmacal Res doi: 10.1007/s12272-019-01115-2 – volume: 40 start-page: 139 year: 2012 ident: 822_CR85 publication-title: Biochem Soc Trans doi: 10.1042/BST20110609 – volume: 22 start-page: 631 issue: 5 year: 2020 ident: 822_CR122 publication-title: Clin Transl Oncol doi: 10.1007/s12094-019-02187-8 – volume: 280 start-page: 630 issue: 2 year: 2016 ident: 822_CR51 publication-title: Radiology doi: 10.1148/radiol.2016150719 – volume: 6 start-page: 33709 year: 2016 ident: 822_CR158 publication-title: Sci Rep doi: 10.1038/srep33709 – volume: 499 start-page: 482 issue: 3 year: 2018 ident: 822_CR68 publication-title: Biochem Biophys Res Commun doi: 10.1016/j.bbrc.2018.03.174 – volume: 6 start-page: 17 issue: 1 year: 2019 ident: 822_CR177 publication-title: Medicines doi: 10.3390/medicines6010017 – volume: 56 start-page: 1687 issue: 10 year: 2020 ident: 822_CR79 publication-title: Sep Sci Technol – volume: 15 start-page: 1325 issue: 10 year: 2015 ident: 822_CR108 publication-title: Expert Rev Mol Diagn doi: 10.1586/14737159.2015.1084229 – volume: 27 start-page: 16 year: 2014 ident: 822_CR141 publication-title: Curr Opin Immunol doi: 10.1016/j.coi.2014.01.004 – volume: 816 start-page: 223 issue: 1–2 year: 2005 ident: 822_CR39 publication-title: B Anal Technol Biomed Life Sci doi: 10.1016/j.jchromb.2004.11.036 – volume: 15 start-page: e0240533 issue: 10 year: 2020 ident: 822_CR156 publication-title: PLoS ONE doi: 10.1371/journal.pone.0240533 – volume: 67 start-page: 194 issue: 3 year: 2017 ident: 822_CR6 publication-title: CA Cancer J Clin doi: 10.3322/caac.21397 – volume: 41 start-page: 211 issue: 3 year: 2016 ident: 822_CR123 publication-title: Trends Biochem Sci doi: 10.1016/j.tibs.2015.12.001 – volume: 19 start-page: 2334 issue: 25 year: 2019 ident: 822_CR18 publication-title: Curr Top Med Chem doi: 10.2174/1568026619666191018100848 – volume: 14 start-page: 1093 issue: 6 year: 2021 ident: 822_CR24 publication-title: Curr Mol Pharmacol doi: 10.2174/1874467214666210120153348 – volume: 10 start-page: 5 issue: 1 year: 2011 ident: 822_CR129 publication-title: Horm-Int J Endocrinol Metab – volume: 15 start-page: 193 issue: 5 year: 2004 ident: 822_CR21 publication-title: Trends Endocrinol Metab doi: 10.1016/j.tem.2004.05.011 – volume: 10 start-page: 669 issue: 6 year: 2021 ident: 822_CR31 publication-title: Clin Pharmacol Drug Dev doi: 10.1002/cpdd.877 – volume: 23 start-page: 9077 issue: 16 year: 2022 ident: 822_CR57 publication-title: Int J Mol Sci doi: 10.3390/ijms23169077 – volume: 19 start-page: 237 issue: 4 year: 2022 ident: 822_CR145 publication-title: Nat Rev Clin Oncol doi: 10.1038/s41571-021-00588-9 – volume: 9 start-page: 84 issue: 1 year: 2020 ident: 822_CR93 publication-title: J Clin Med doi: 10.3390/jcm9010084 – volume: 2016 start-page: 5738694 year: 2016 ident: 822_CR48 publication-title: Evid-Based Compl Altern Med doi: 10.1155/2016/5738694 – volume: 121 start-page: 2750 issue: 7 year: 2011 ident: 822_CR3 publication-title: J Clin Invest doi: 10.1172/JCI45014 – volume: 16 start-page: 20 issue: 1 year: 2016 ident: 822_CR54 publication-title: Nat Rev Cancer doi: 10.1038/nrc.2015.2 – volume: 54 start-page: 561 issue: 4 year: 2016 ident: 822_CR159 publication-title: Pharm Biol doi: 10.3109/13880209.2015.1101142 – volume: 17 start-page: 395 issue: 7 year: 2020 ident: 822_CR55 publication-title: Nat Rev Clin Oncol doi: 10.1038/s41571-020-0341-y – volume: 46 start-page: 1333 issue: 06 year: 2018 ident: 822_CR117 publication-title: Am J Chin Med doi: 10.1142/S0192415X18500702 – volume: 11 start-page: 118 issue: 1 year: 2021 ident: 822_CR114 publication-title: Biomolecules doi: 10.3390/biom11010118 – volume: 1868 start-page: 584 issue: 2 year: 2017 ident: 822_CR155 publication-title: Biochim Biophys Acta-Rev Cancer doi: 10.1016/j.bbcan.2017.06.006 – volume: 15 start-page: 299 issue: 6 year: 2010 ident: 822_CR22 publication-title: J Res Med Sci – volume: 9 start-page: 5513 issue: 11 year: 2018 ident: 822_CR60 publication-title: Food Funct doi: 10.1039/C8FO01122B – volume: 12 start-page: 31 issue: 1 year: 2022 ident: 822_CR12 publication-title: Cancer Discov doi: 10.1158/2159-8290.CD-21-1059 – volume: 154 start-page: 753 issue: 3 year: 2014 ident: 822_CR44 publication-title: J Ethnopharmacol doi: 10.1016/j.jep.2014.04.051 – volume: 15 start-page: 178 issue: 2 year: 2021 ident: 822_CR121 publication-title: Front Med doi: 10.1007/s11684-020-0793-6 – volume: 5 start-page: 1205 issue: 8 year: 2019 ident: 822_CR143 publication-title: JAMA Oncol doi: 10.1001/jamaoncol.2018.7147 – volume: 14 start-page: 155 issue: 3 year: 2017 ident: 822_CR133 publication-title: Nat Rev Clin Oncol doi: 10.1038/nrclinonc.2016.144 – volume: 3 start-page: 21 issue: 1 year: 2021 ident: 822_CR125 publication-title: Nat Metab doi: 10.1038/s42255-020-00317-z – volume: 72 start-page: 76 year: 2021 ident: 822_CR140 publication-title: Semin Cancer Biol doi: 10.1016/j.semcancer.2019.12.018 – volume: 124 start-page: 109891 year: 2020 ident: 822_CR132 publication-title: Biomed Pharmacother doi: 10.1016/j.biopha.2020.109891 – volume: 14 start-page: 633 issue: 7 year: 2021 ident: 822_CR102 publication-title: Pharmaceuticals doi: 10.3390/ph14070633 – volume: 14 start-page: 1 year: 2015 ident: 822_CR92 publication-title: Mol Cancer – volume: 32 start-page: 1227 issue: 6 year: 2013 ident: 822_CR53 publication-title: Int J Mol Med doi: 10.3892/ijmm.2013.1519 – volume: 43 start-page: 625 issue: 4 year: 2019 ident: 822_CR113 publication-title: J Ginseng Res doi: 10.1016/j.jgr.2019.02.004 – volume: 2022 start-page: 1 year: 2022 ident: 822_CR167 publication-title: Biomed Res Int – volume: 13 start-page: 17177 issue: 13 year: 2021 ident: 822_CR149 publication-title: Aging doi: 10.18632/aging.203131 – volume: 7 start-page: 70535 issue: 43 year: 2016 ident: 822_CR171 publication-title: Oncotarget doi: 10.18632/oncotarget.12059 – volume: 10 start-page: 235 issue: 3 year: 2017 ident: 822_CR99 publication-title: Cell Mol Bioeng doi: 10.1007/s12195-017-0485-8 – volume: 23 start-page: 2288 issue: 4 year: 2022 ident: 822_CR8 publication-title: Int J Mol Sci doi: 10.3390/ijms23042288 – volume: 138 start-page: 623 issue: 4 year: 2009 ident: 822_CR100 publication-title: Cell doi: 10.1016/j.cell.2009.08.007 – volume: 14 start-page: 474 issue: 3 year: 2022 ident: 822_CR111 publication-title: Cancers doi: 10.3390/cancers14030474 – volume: 11 start-page: 940 year: 2020 ident: 822_CR138 publication-title: Front Immunol doi: 10.3389/fimmu.2020.00940 – volume: 42 start-page: 455 issue: 4 year: 2018 ident: 822_CR118 publication-title: J Ginseng Res doi: 10.1016/j.jgr.2017.05.003 – volume: 202 start-page: 115101 year: 2022 ident: 822_CR130 publication-title: Biochem Pharmacol doi: 10.1016/j.bcp.2022.115101 – volume: 45 start-page: 174 issue: 3 year: 2022 ident: 822_CR71 publication-title: Arch Pharm Res doi: 10.1007/s12272-022-01377-3 – volume: 35 start-page: e9083 issue: 11 year: 2021 ident: 822_CR38 publication-title: Rapid Commun Mass Spectrom doi: 10.1002/rcm.9083 – volume: 89 start-page: 227 year: 2017 ident: 822_CR58 publication-title: Biomed Pharmacother doi: 10.1016/j.biopha.2017.02.038 – volume: 13 start-page: 788 issue: 11 year: 2013 ident: 822_CR84 publication-title: Nat Rev Cancer doi: 10.1038/nrc3603 – volume: 132 start-page: 2724 issue: 22 year: 2019 ident: 822_CR166 publication-title: Chin Med J doi: 10.1097/CM9.0000000000000498 – volume: 57 start-page: 255 year: 2019 ident: 822_CR62 publication-title: J Funct Foods doi: 10.1016/j.jff.2019.04.019 – volume: 38 start-page: 182 issue: 2 year: 2022 ident: 822_CR106 publication-title: Trends Genet doi: 10.1016/j.tig.2021.06.014 – volume: 37 start-page: 2445 issue: 16 year: 2015 ident: 822_CR52 publication-title: Hebei Med J – volume: 7 start-page: 6173 issue: 15 year: 2015 ident: 822_CR33 publication-title: Anal Methods doi: 10.1039/C5AY01365H – volume: 7 start-page: 35144 issue: 23 year: 2016 ident: 822_CR91 publication-title: Oncotarget doi: 10.18632/oncotarget.9059 – volume: 236 start-page: 153956 year: 2022 ident: 822_CR15 publication-title: Pathol Res Pract doi: 10.1016/j.prp.2022.153956 – volume: 20 start-page: 8069 issue: 21 year: 2000 ident: 822_CR86 publication-title: Mol Cell Biol doi: 10.1128/MCB.20.21.8069-8083.2000 – volume: 10 start-page: 528 issue: 4 year: 2020 ident: 822_CR157 publication-title: Biomolecules doi: 10.3390/biom10040528 – volume: 19 start-page: 3466 issue: 11 year: 2018 ident: 822_CR74 publication-title: Int J Mol Sci doi: 10.3390/ijms19113466 – volume: 43 start-page: 527 issue: 4 year: 2019 ident: 822_CR90 publication-title: J Ginseng Res doi: 10.1016/j.jgr.2018.03.004 – volume: 5 start-page: 19 year: 2010 ident: 822_CR36 publication-title: Chin Med doi: 10.1186/1749-8546-5-19 – volume: 49 start-page: 2229 issue: 9 year: 2011 ident: 822_CR43 publication-title: Food Chem Toxicol doi: 10.1016/j.fct.2011.06.020 – volume: 35 start-page: S25 year: 2015 ident: 822_CR82 publication-title: Semin Cancer Biol doi: 10.1016/j.semcancer.2015.02.006 – volume: 54 start-page: 647 issue: 5 year: 2022 ident: 822_CR89 publication-title: Acta Biochim Biophys Sin doi: 10.3724/abbs.2022039 – volume: 47 start-page: 99 issue: 1 year: 2020 ident: 822_CR67 publication-title: Clin Exp Obstet Gynecol – volume: 38 start-page: 359 issue: 1 year: 2017 ident: 822_CR94 publication-title: Oncol Rep doi: 10.3892/or.2017.5652 – volume: 43 start-page: 421 issue: 3 year: 2019 ident: 822_CR101 publication-title: J Ginseng Res doi: 10.1016/j.jgr.2018.05.004 – volume: 8 start-page: 5574 issue: 12 year: 2019 ident: 822_CR151 publication-title: Cancer Med doi: 10.1002/cam4.2474 – volume: 3 start-page: e2697 issue: 7 year: 2008 ident: 822_CR35 publication-title: PLoS ONE doi: 10.1371/journal.pone.0002697 – volume: 85 start-page: 297M issue: 3 year: 2014 ident: 822_CR161 publication-title: Radiol Technol – volume: 36 start-page: 102 issue: 1 year: 2012 ident: 822_CR47 publication-title: J Ginseng Res doi: 10.5142/jgr.2012.36.1.102 – volume: 47 start-page: 1643 issue: 7 year: 2019 ident: 822_CR115 publication-title: Am J Chin Med doi: 10.1142/S0192415X19500848 – volume: 35 start-page: 515 issue: 3 year: 2014 ident: 822_CR124 publication-title: Carcinogenesis doi: 10.1093/carcin/bgt480 – volume: 4 start-page: 529 issue: 3 year: 2016 ident: 822_CR178 publication-title: J Mater Chem B doi: 10.1039/C5TB02305J – volume: 12 start-page: 797634 year: 2021 ident: 822_CR16 publication-title: Front Pharmacol doi: 10.3389/fphar.2021.797634 – volume: 44 start-page: 1099 issue: 12 year: 2014 ident: 822_CR42 publication-title: Xenobiotica doi: 10.3109/00498254.2014.929192 – volume: 103 year: 2020 ident: 822_CR69 publication-title: Bioorg Chem – volume: 12 start-page: 445 issue: 8 year: 2015 ident: 822_CR98 publication-title: Nat Rev Clin Oncol doi: 10.1038/nrclinonc.2015.61 – volume: 83 start-page: 152 year: 2022 ident: 822_CR112 publication-title: Semin Cancer Biol doi: 10.1016/j.semcancer.2020.08.009 – volume: 100 start-page: 57 issue: 1 year: 2000 ident: 822_CR19 publication-title: Cell doi: 10.1016/S0092-8674(00)81683-9 – volume: 22 start-page: 851 issue: 7 year: 2008 ident: 822_CR27 publication-title: Phytother Res doi: 10.1002/ptr.2384 – volume: 395 start-page: 817 issue: 10226 year: 2020 ident: 822_CR88 publication-title: Lancet doi: 10.1016/S0140-6736(20)30165-3 – volume: 13 start-page: 1892 issue: 8 year: 2021 ident: 822_CR70 publication-title: Cancers doi: 10.3390/cancers13081892 – volume: 28 start-page: 419 issue: 3 year: 2014 ident: 822_CR32 publication-title: Biomed Chromatogr doi: 10.1002/bmc.3037 – volume: 36 start-page: 170 issue: 3 year: 2001 ident: 822_CR40 publication-title: Yao xue xue bao = Acta Pharm Sin – volume: 9 start-page: 180 issue: 2 year: 2016 ident: 822_CR95 publication-title: Asian Pac J Trop Med doi: 10.1016/j.apjtm.2016.01.010 – volume: 16 start-page: 2587 issue: 29 year: 2021 ident: 822_CR170 publication-title: Nanomedicine doi: 10.2217/nnm-2021-0329 – volume: 43 start-page: 773 issue: 8 year: 2020 ident: 822_CR174 publication-title: Arch Pharmacal Res doi: 10.1007/s12272-020-01265-8 – volume: 10 start-page: 101 issue: 4 year: 2018 ident: 822_CR105 publication-title: Cancers doi: 10.3390/cancers10040101 |
SSID | ssj0053538 |
Score | 2.3615172 |
SecondaryResourceType | review_article |
Snippet | In 2021, breast cancer accounted for a substantial proportion of cancer cases and represented the second leading cause of cancer deaths among women worldwide.... Abstract In 2021, breast cancer accounted for a substantial proportion of cancer cases and represented the second leading cause of cancer deaths among women... |
SourceID | doaj pubmedcentral proquest gale crossref springer |
SourceType | Open Website Open Access Repository Aggregation Database Enrichment Source Index Database Publisher |
StartPage | 1 |
SubjectTerms | Acupuncture Angiogenesis Apoptosis Bone density Breast cancer Cancer Cancer cells Cancer therapies Care and treatment Cell death Cell growth Chemotherapy Clinical medicine Complementary & Alternative Medicine Development and progression Drugs Epithelial-mesenchymal transition Genetic aspects Ginsenoside Ginsenosides Hallmarks of cancer Health aspects Herbal medicine Inflammation Medical research Medicine Medicine & Public Health Metastasis Oncology, Experimental Pathogenesis Patients Physiological aspects Quality of life Review Structure-function relationships Toxicity Traditional Chinese Medicine Tumor cells Tumors |
SummonAdditionalLinks | – databaseName: DOAJ Directory of Open Access Journals dbid: DOA link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrR1Lb9YwLEI7IC6IpygMCBISB4jWJmmachuIMSGNE5N2i1I3EZ_G2ulrx-_HTtsPygRcuDZO2voR24kfjL1salWDllpIH0HoIEthQ4wi5kp628o8AiUnn3w2x6f601l59kurL4oJm8oDT4g7aFAarW0KXKFB6xxddFOCgqh9rbyOqXopqrHFmZr24FKhHC8pMtYcDHQ9lwvUTyKVOBf1Sg2lav3X9-TrcZK_XZYmHXR0h92ejUd-OH30XXYjdPfYzZP5evw-O_-4oaPinlpwDm95SurFhTgaeRzV1QY4tU658NvzgfeRA1F8y-nsfuBjzymuMnwPCfwSCdAPgcBSLDot01AA-zhPe8BOjz58eX8s5m4KAkxhRtHmQVe5r41soVXKK5171F8FoEkY0Y2JiprQVEpCaAtTmdbE3II2AUr00aqgHrK9ru_CI8YLHWNDplfwUlswvgZVNKpsoDTRFnnGigW5DuZS49Tx4ptLLoc1biKIQ4K4RBBXZ-z1bs7lVGjjr9DviGY7SCqSnR4g67iZddy_WCdjz4nibso43Ym6O6zQp1MK94-MvUoQJOz4A-DnnAVEA5XNWkHuryBRSGE9vHCVmzeJwaGzWmk0B22VsRe7YZpJgW9d6K8IxtQSGZyQalfcuPr39Ui3-ZoKhaPtXJA9mrE3C-P-fPufkfv4fyD3Cbslk7zVQpb7bG_cXoWnaL-NzbMkqj8AMUA_MA priority: 102 providerName: Directory of Open Access Journals – databaseName: Springer Nature OA Free Journals dbid: C6C link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlR1da9UwNOgE8UX8xOrUCIIPGmw-mia-zYtzCPPJwd5CmiZ42WzHbefv95zc9mqdCr42Jy093yc5H4S8bKy0QQnFhE-BqSgqZmJKLJVSeNOKMgUsTj7-rI9O1KfT6nRqk4O1ML_e33Oj3w54sVYysCwsNydn9jq5UcFDTN9b6dWsdSsJkjsXxfxx38Lw5P78V7Xw1czI365Hs9U5vENuT-4iPdjS9y65Frt75ObxdCF-n5x9XOPhcI9DN4d3NJfxwosouHUUDNQ6UByW8s1vzgbaJxqQxhuKp_UDHXuKmZTxe8zgF4DyfogIlrPP8TUNpqyP07YH5OTww5fVEZvmJ7CguR5ZW0ZVl95q0YZWSi9V6cFi8QBOYILAJUkcO1NLEWLLda1bnUoTlI6hgqisjvIh2ev6Lj4ilKuUGnS2ohfKBO1tkLyRVRMqnQwvC8Jn5LowNRfHGRfnLgcZRrstQRwQxGWCOFuQ17s9F9vWGv-Efo8020FiW-z8ALjFTVLmGlDdxjQc2K2BUE5acLCCDEl5K71KVUGeI8XdtsZ0J9zuoIYoTkrQGAV5lSFQvOEHgp-qFAAN2ChrAbm_gASxDMvlmavcpBYGB-FprcABNHVBXuyWcSemunWxv0QYbYUoM1LNghsX_75c6dZfc2tw8JY5eqAFeTMz7s-v_x25j_8P_Am5JbJkWSaqfbI3bi7jU_DNxuZZFsof654vkw priority: 102 providerName: Springer Nature |
Title | Ginsenosides: changing the basic hallmarks of cancer cells to achieve the purpose of treating breast cancer |
URI | https://link.springer.com/article/10.1186/s13020-023-00822-9 https://www.proquest.com/docview/2877497687 https://www.proquest.com/docview/2869220810 https://pubmed.ncbi.nlm.nih.gov/PMC10518937 https://doaj.org/article/b91188b18efb49939065c3cf4a93a4f5 |
Volume | 18 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
journalDatabaseRights | – providerCode: PRVADU databaseName: BioMedCentral customDbUrl: eissn: 1749-8546 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0053538 issn: 1749-8546 databaseCode: RBZ dateStart: 20060101 isFulltext: true titleUrlDefault: https://www.biomedcentral.com/search/ providerName: BioMedCentral – providerCode: PRVAON databaseName: DOAJ Directory of Open Access Journals customDbUrl: eissn: 1749-8546 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0053538 issn: 1749-8546 databaseCode: DOA dateStart: 20060101 isFulltext: true titleUrlDefault: https://www.doaj.org/ providerName: Directory of Open Access Journals – providerCode: PRVEBS databaseName: EBSCOhost Academic Search Ultimate customDbUrl: https://search.ebscohost.com/login.aspx?authtype=ip,shib&custid=s3936755&profile=ehost&defaultdb=asn eissn: 1749-8546 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0053538 issn: 1749-8546 databaseCode: ABDBF dateStart: 20090101 isFulltext: true titleUrlDefault: https://search.ebscohost.com/direct.asp?db=asn providerName: EBSCOhost – providerCode: PRVBFR databaseName: Free Medical Journals customDbUrl: eissn: 1749-8546 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0053538 issn: 1749-8546 databaseCode: DIK dateStart: 20060101 isFulltext: true titleUrlDefault: http://www.freemedicaljournals.com providerName: Flying Publisher – providerCode: PRVFQY databaseName: GFMER Free Medical Journals customDbUrl: eissn: 1749-8546 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0053538 issn: 1749-8546 databaseCode: GX1 dateStart: 0 isFulltext: true titleUrlDefault: http://www.gfmer.ch/Medical_journals/Free_medical.php providerName: Geneva Foundation for Medical Education and Research – providerCode: PRVAQN databaseName: PubMed Central customDbUrl: eissn: 1749-8546 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0053538 issn: 1749-8546 databaseCode: RPM dateStart: 20060101 isFulltext: true titleUrlDefault: https://www.ncbi.nlm.nih.gov/pmc/ providerName: National Library of Medicine – providerCode: PRVPQU databaseName: Health & Medical Collection customDbUrl: eissn: 1749-8546 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0053538 issn: 1749-8546 databaseCode: 7X7 dateStart: 20090101 isFulltext: true titleUrlDefault: https://search.proquest.com/healthcomplete providerName: ProQuest – providerCode: PRVPQU databaseName: ProQuest Central customDbUrl: http://www.proquest.com/pqcentral?accountid=15518 eissn: 1749-8546 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0053538 issn: 1749-8546 databaseCode: BENPR dateStart: 20090101 isFulltext: true titleUrlDefault: https://www.proquest.com/central providerName: ProQuest – providerCode: PRVAVX databaseName: Springer Nature HAS Fully OA customDbUrl: eissn: 1749-8546 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0053538 issn: 1749-8546 databaseCode: AAJSJ dateStart: 20061201 isFulltext: true titleUrlDefault: https://www.springernature.com providerName: Springer Nature – providerCode: PRVAVX databaseName: Springer Nature OA Free Journals customDbUrl: eissn: 1749-8546 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0053538 issn: 1749-8546 databaseCode: C6C dateStart: 20061201 isFulltext: true titleUrlDefault: http://www.springeropen.com/ providerName: Springer Nature |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3db9MwELdgkxAviE8RGCVISDyAtcR2HJsX1FUbU6VNCJi0N8tx7FENmtJ0_P3cuW6nMLGnSsk5TXxfv7PPd4S8bTTXTjBBmQ2OCs8qqnwINBScWdWyIjg8nHxyKo_PxPS8Ok8Lbn1Kq9zYxGio287hGvk-IPtagO9U9afFb4pdo3B3NbXQuEt2S4AqKNX1-TbgqngVO1kD6NZUVUJuDs0oud_jhl1BwWPRWPSc6oFjivX7b1rpm5mT_2yfRq909JA8SHAyH6_5_4jc8fPH5N5J2jB_Qi4_z3DxuMOmnP3HPB7zhQflAPtycGAzl2MzlV92ednnXcgdysAyx9X8Pl91OWZa-j8-ki-AJV3vkSxmp-NjGkxpX6VhT8nZ0eH3yTFN_RWok6Vc0bbwoi6slqx1LeeWi8KCRysdgMQAgU3g2Jam5sz5tpS1bGUolBPSuwqittrzZ2Rn3s39c5KXIoQGwZi3TCgnrXa8bHjVuEoGVRYZKTeTa1wqPo49MH6aGIQoadYMMcAQExlidEbeb8cs1qU3bqU-QJ5tKbFsdrzQLS9M0kLTgGlXqilBHBsI9bgGAOa4C8JqbkWoMvIaOW7WZ1C3ym_GNUR5nINFyci7SIHqDx_gbDrFANOAhbQGlHsDSlBbN7y9kSqTzEZvroU8I2-2t3EkpsLNfXeFNFIzVsRJVQNpHHz78M589iOWDgc0XSJCzciHjeBe__v_J_fF7S_7ktxnUZM0ZdUe2Vktr_wrwGqrZhQVckR2x-Pptyn8HhyefvkKVydyMorrH38B0ws95w |
linkProvider | ProQuest |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9QwELZKkYAL4ikChRoJxAGsJrbjOEgIlUfZ0m5PrbQ3N3FsWBU2y2YL4k_xG5lxkq1CRW-9rsfOxjOe-SaeByHPylzkVnLJeOEtk46nTDvvmY8FL3TFY28xOXl8oEZH8vMknayRP30uDIZV9joxKOqqtviNfAuQfSbBdurs7fwHw65ReLvat9BoxWLP_f4FLlvzZvcD8Pc55zsfD9-PWNdVgFmVqCWrYiezuMgVr2wlRCFkXIAeTyxAIw9w3gtsxpIJbl2VqExVysfaSuVsCr5K5gSse4VclSKWWKs_m6wcvFSkoXM2gPyc6VSqPklHq60GLwhjBhaShSLrLB8YwtAv4LxVOB-p-c91bbCCO7fIzQ6-0u1W3m6TNTe7Q66Nuwv6u-Tk0xQ_VtfYBLR5TUNaMSxEAWZSMJhTS7F5y_dicdLQ2lOLMregeHvQ0GVNMbLT_XSBfA4iUDcOyUI0PC5TYgj9spt2jxxdys7fJ-uzeuYeEJpI70sEf67gUltV5FYkpUhLmyqvkzgiSb-5xnbFzrHnxjcTnB6tTMsQAwwxgSEmj8jL1Zx5W-rjQup3yLMVJZbpDj_Uiy-mO_WmBFOidZmA-JfgWoocAJ8V1ssiF4X0aUQ2keOmzXldKRuznYFXKQRosIi8CBSobuAFbNFlTcA2YOGuAeXGgBLUhB0O91JlOjXVmLNDFZGnq2GciaF3M1efIo3KOY_DpuqBNA7efTgym34NpcoBvSeIiCPyqhfcs6f_f3MfXvxnN8n10eF43-zvHuw9Ijd4OFU54-kGWV8uTt1jwInL8kk4nJQcX7Y2-AsnTnPj |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV1Lb9QwELaglSouiKcILTRISBwgamI7js1teSxloRUSVOrNchy7rEqT1Sbl9zPjJAuhgMQ1_pwoHs_LngchT0vFlOWUJ9R4m3BH80Q67xOfMmpkRVNvMTn56FgcnvDFaX76SxZ_iHYfryT7nAas0lR3B6vK9ywuxUGL121pAvomCSXLE3WdbMtcCXC_tmezxefFKI1zBhw9Jsv8ceZEIYW6_Vel89WIyd-uTYM2mt8iNwczMp71dL9Nrrn6Dtk5Gi7K75Lzd0s8NG6wGWf7Mg7pvfCiGMy9GBTX0sbYROXCrM_buPGxRdqvYzzFb-OuiTHC0n13Ab4CUjStQ1iISsfXlBjK3g3T7pGT-dsvrw-Toa9CYkUmuqRKHS9SowStbMWYYTw1oMkyC8ahB4fGM2xHUzBqXZWJQlTCp9Jy4WwO3lrh2H2yVTe1e0DijHtfohHmDOXSCqMsy0qWlzYXXmZpRLJxcbUdio5j74tvOjgfUuieIBoIogNBtIrI882cVV9y45_oV0izDRLLZYcHzfpMD9ynSxDpUpYZbMMSXDymwPCyzHpuFDPc5xHZR4rrPvd0w_R6VoB3xxhIkog8Cwhke_gBa4bsBVgGLKA1Qe5NkMCudjo87io9iItWg9tacDAMZRGRJ5thnIkhcLVrLhEjFKVpWFQ52Y2Tf5-O1MuvoWQ4WNEZWqYReTFu3J9f__viPvw_-D7Z-fRmrj--P_6wS27QwGQqofke2erWl-4RmG9d-Xjg0B9myjw- |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Ginsenosides%3A+changing+the+basic+hallmarks+of+cancer+cells+to+achieve+the+purpose+of+treating+breast+cancer&rft.jtitle=Chinese+medicine&rft.au=Jiang%2C+Rui-yuan&rft.au=Fang%2C+Zi-ru&rft.au=Zhang%2C+Huan-ping&rft.au=Xu%2C+Jun-yao&rft.date=2023-09-25&rft.pub=BioMed+Central+Ltd&rft.issn=1749-8546&rft.eissn=1749-8546&rft.volume=18&rft.issue=1&rft_id=info:doi/10.1186%2Fs13020-023-00822-9&rft.externalDocID=A766633200 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1749-8546&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1749-8546&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1749-8546&client=summon |