MicroRNA-219-5p Promotes Tumor Growth and Metastasis of Hepatocellular Carcinoma by Regulating Cadherin 1
MicroRNAs play significant roles in the development of cancer and may serve as promising therapeutic targets. In our previous work, miR-219-5p was identified as one of the important metastasis-related microRNAs in HCC. Here we demonstrated that miR-219-5p expression was elevated in HCC tissues and w...
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Published in | BioMed research international Vol. 2018; no. 2018; pp. 1 - 10 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Cairo, Egypt
Hindawi Publishing Corporation
01.01.2018
Hindawi John Wiley & Sons, Inc |
Subjects | |
Online Access | Get full text |
ISSN | 2314-6133 2314-6141 2314-6141 |
DOI | 10.1155/2018/4793971 |
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Abstract | MicroRNAs play significant roles in the development of cancer and may serve as promising therapeutic targets. In our previous work, miR-219-5p was identified as one of the important metastasis-related microRNAs in HCC. Here we demonstrated that miR-219-5p expression was elevated in HCC tissues and was associated with vascular invasion and dismal prognosis. In multivariate analysis, miR-219-5p was identified as an independent prognostic indicator for HCC patients. Functional mechanism analyses showed that miR-219-5p promoted HCC cell proliferation and invasion in in vitro, as well as in vivo, tumor growth and metastasis in nude mice models bearing human HCC tumors. In addition, cadherin 1 (CDH1) was revealed to be a downstream target of miR-219-5p in HCC cells. In conclusion, miR-219-5p promotes tumor growth and metastasis of HCC by regulating CDH1 and can serve as a prognostic marker for HCC patients. |
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AbstractList | MicroRNAs play significant roles in the development of cancer and may serve as promising therapeutic targets. In our previous work, miR-219-5p was identified as one of the important metastasis-related microRNAs in HCC. Here we demonstrated that miR-219-5p expression was elevated in HCC tissues and was associated with vascular invasion and dismal prognosis. In multivariate analysis, miR-219-5p was identified as an independent prognostic indicator for HCC patients. Functional mechanism analyses showed that miR-219-5p promoted HCC cell proliferation and invasion in in vitro, as well as in vivo, tumor growth and metastasis in nude mice models bearing human HCC tumors. In addition, cadherin 1 (CDH1) was revealed to be a downstream target of miR-219-5p in HCC cells. In conclusion, miR-219-5p promotes tumor growth and metastasis of HCC by regulating CDH1 and can serve as a prognostic marker for HCC patients. MicroRNAs play significant roles in the development of cancer and may serve as promising therapeutic targets. In our previous work, miR-219-5p was identified as one of the important metastasis-related microRNAs in HCC. Here we demonstrated that miR-219-5p expression was elevated in HCC tissues and was associated with vascular invasion and dismal prognosis. In multivariate analysis, miR-219-5p was identified as an independent prognostic indicator for HCC patients. Functional mechanism analyses showed that miR-219-5p promoted HCC cell proliferation and invasion in in vitro , as well as in vivo , tumor growth and metastasis in nude mice models bearing human HCC tumors. In addition, cadherin 1 (CDH1) was revealed to be a downstream target of miR-219-5p in HCC cells. In conclusion, miR-219-5p promotes tumor growth and metastasis of HCC by regulating CDH1 and can serve as a prognostic marker for HCC patients. MicroRNAs play significant roles in the development of cancer and may serve as promising therapeutic targets. In our previous work, miR-219-5p was identified as one of the important metastasis-related microRNAs in HCC. Here we demonstrated that miR-219-5p expression was elevated in HCC tissues and was associated with vascular invasion and dismal prognosis. In multivariate analysis, miR-219-5p was identified as an independent prognostic indicator for HCC patients. Functional mechanism analyses showed that miR-219-5p promoted HCC cell proliferation and invasion in in vitro, as well as in vivo, tumor growth and metastasis in nude mice models bearing human HCC tumors. In addition, cadherin 1 (CDH1) was revealed to be a downstream target of miR-219-5p in HCC cells. In conclusion, miR-219-5p promotes tumor growth and metastasis of HCC by regulating CDH1 and can serve as a prognostic marker for HCC patients.MicroRNAs play significant roles in the development of cancer and may serve as promising therapeutic targets. In our previous work, miR-219-5p was identified as one of the important metastasis-related microRNAs in HCC. Here we demonstrated that miR-219-5p expression was elevated in HCC tissues and was associated with vascular invasion and dismal prognosis. In multivariate analysis, miR-219-5p was identified as an independent prognostic indicator for HCC patients. Functional mechanism analyses showed that miR-219-5p promoted HCC cell proliferation and invasion in in vitro, as well as in vivo, tumor growth and metastasis in nude mice models bearing human HCC tumors. In addition, cadherin 1 (CDH1) was revealed to be a downstream target of miR-219-5p in HCC cells. In conclusion, miR-219-5p promotes tumor growth and metastasis of HCC by regulating CDH1 and can serve as a prognostic marker for HCC patients. MicroRNAs play significant roles in the development of cancer and may serve as promising therapeutic targets. In our previous work, miR-219-5p was identified as one of the important metastasis-related microRNAs in HCC. Here we demonstrated that miR-219-5p expression was elevated in HCC tissues and was associated with vascular invasion and dismal prognosis. In multivariate analysis, miR-219-5p was identified as an independent prognostic indicator for HCC patients. Functional mechanism analyses showed that miR-219-5p promoted HCC cell proliferation and invasion in , as well as , tumor growth and metastasis in nude mice models bearing human HCC tumors. In addition, cadherin 1 (CDH1) was revealed to be a downstream target of miR-219-5p in HCC cells. In conclusion, miR-219-5p promotes tumor growth and metastasis of HCC by regulating CDH1 and can serve as a prognostic marker for HCC patients. |
Audience | Academic |
Author | Zhu, Ying Wei, Jin-Wang Gao, Xiao-Mei Dong, Qiong Z. Yang, Jing Jia, Hu-Liang Sheng, Yuan-Yuan Qin, Lun-Xiu |
AuthorAffiliation | 2 Institutes of Biomedical Sciences, Fudan University, 131 Dong An Road, Shanghai 200032, China 1 Department of General Surgery, Huashan Hospital, Cancer Metastasis Institute, Fudan University, 12 Urumqi Road (M), Shanghai 200040, China |
AuthorAffiliation_xml | – name: 1 Department of General Surgery, Huashan Hospital, Cancer Metastasis Institute, Fudan University, 12 Urumqi Road (M), Shanghai 200040, China – name: 2 Institutes of Biomedical Sciences, Fudan University, 131 Dong An Road, Shanghai 200032, China |
Author_xml | – sequence: 1 fullname: Qin, Lun-Xiu – sequence: 2 fullname: Jia, Hu-Liang – sequence: 3 fullname: Zhu, Ying – sequence: 4 fullname: Gao, Xiao-Mei – sequence: 5 fullname: Wei, Jin-Wang – sequence: 6 fullname: Sheng, Yuan-Yuan – sequence: 7 fullname: Yang, Jing – sequence: 8 fullname: Dong, Qiong Z. |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29862272$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1155_2018_8730593 crossref_primary_10_1007_s11033_023_08586_z crossref_primary_10_1080_21505594_2024_2421231 crossref_primary_10_1136_bmjopen_2022_064700 crossref_primary_10_1080_15384047_2020_1843897 crossref_primary_10_2147_IJGM_S309436 crossref_primary_10_1186_s11658_018_0129_6 crossref_primary_10_1042_BSR20210318 crossref_primary_10_1515_oncologie_2023_0024 |
Cites_doi | 10.1093/carcin/bgs235 10.1002/(SICI)1098-1004(1998)12:4<226::AID-HUMU2>3.0.CO;2-D 10.1016/j.jhep.2016.05.007 10.3892/ol.2017.5570 10.1073/pnas.0500918102 10.1016/S0140-6736(09)60381-0 10.1002/hep.26095 10.1158/0008-5472.CAN-07-2938 10.1016/S1470-2045(12)70073-6 10.1038/nrm3758 10.7314/APJCP.2012.13.12.6455 10.3748/wjg.v8.i3.385 10.3892/mmr.2014.2194 10.1053/j.gastro.2011.02.006 10.1016/j.jprot.2012.10.016 10.1002/hep.23904 10.3390/jcm5030030 10.1002/hep.22160 10.3322/caac.21166 10.3727/096504016X14768374457986 10.1007/s10555-008-9169-0 10.1038/nrm1699 10.1158/0008-5472.CAN-06-4607 10.1016/j.semcdb.2017.12.011 10.1016/0092-8674(91)90143-M 10.1053/jhep.2002.35342 |
ContentType | Journal Article |
Copyright | Copyright © 2018 Jing Yang et al. COPYRIGHT 2018 John Wiley & Sons, Inc. Copyright © 2018 Jing Yang et al.; This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Copyright © 2018 Jing Yang et al. 2018 |
Copyright_xml | – notice: Copyright © 2018 Jing Yang et al. – notice: COPYRIGHT 2018 John Wiley & Sons, Inc. – notice: Copyright © 2018 Jing Yang et al.; This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. – notice: Copyright © 2018 Jing Yang et al. 2018 |
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SubjectTerms | Analysis Animal models Apoptosis Biology Biomarkers, Tumor - biosynthesis Cadherins Cadherins - biosynthesis Cancer Carcinoma, Hepatocellular - metabolism Carcinoma, Hepatocellular - pathology Cell adhesion & migration Cell cycle Cell growth Cell proliferation Development and progression E-cadherin Female Flow cytometry Gene Expression Regulation, Neoplastic Growth Health aspects Hep G2 Cells Hepatocellular carcinoma Hepatology Humans Laboratory animals Liver cancer Liver Neoplasms - metabolism Liver Neoplasms - pathology Male Manufacturers Medical prognosis Medical research Metastases Metastasis MicroRNA MicroRNAs MicroRNAs - biosynthesis miRNA Multivariate analysis Neoplasm Metastasis Neoplasm Proteins - biosynthesis Patients Prognosis Ribonucleic acid RNA RNA, Neoplasm - biosynthesis Therapeutic applications Tumors |
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Title | MicroRNA-219-5p Promotes Tumor Growth and Metastasis of Hepatocellular Carcinoma by Regulating Cadherin 1 |
URI | https://search.emarefa.net/detail/BIM-1126910 https://dx.doi.org/10.1155/2018/4793971 https://www.ncbi.nlm.nih.gov/pubmed/29862272 https://www.proquest.com/docview/2045214391 https://www.proquest.com/docview/2049938981 https://pubmed.ncbi.nlm.nih.gov/PMC5976989 |
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