Vascular smooth muscle cell proliferation as a therapeutic target. Part 2: Natural products inhibiting proliferation
Many natural products have been so far tested regarding their potency to inhibit vascular smooth muscle cell proliferation, a process involved in atherosclerosis, pulmonary hypertension and restenosis. Compounds studied in vitro and in vivo as VSMC proliferation inhibitors include, for example indir...
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| Published in | Biotechnology advances Vol. 36; no. 6; pp. 1608 - 1621 |
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| Main Authors | , , , , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
England
Elsevier Inc
01.11.2018
Elsevier Science Ltd |
| Subjects | |
| Online Access | Get full text |
| ISSN | 0734-9750 1873-1899 1873-1899 |
| DOI | 10.1016/j.biotechadv.2018.04.002 |
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| Abstract | Many natural products have been so far tested regarding their potency to inhibit vascular smooth muscle cell proliferation, a process involved in atherosclerosis, pulmonary hypertension and restenosis. Compounds studied in vitro and in vivo as VSMC proliferation inhibitors include, for example indirubin-3′-monoxime, resveratrol, hyperoside, plumericin, pelargonidin, zerumbone and apamin. Moreover, taxol and rapamycin, the most prominent compounds applied in drug-eluting stents to counteract restenosis, are natural products. Numerous studies show that natural products have proven to yield effective inhibitors of vascular smooth muscle cell proliferation and ongoing research effort might result in the discovery of further clinically relevant compounds. |
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| AbstractList | Many natural products have been so far tested regarding their potency to inhibit vascular smooth muscle cell proliferation, a process involved in atherosclerosis, pulmonary hypertension and restenosis. Compounds studied in vitro and in vivo as VSMC proliferation inhibitors include, for example indirubin-3′-monoxime, resveratrol, hyperoside, plumericin, pelargonidin, zerumbone and apamin. Moreover, taxol and rapamycin, the most prominent compounds applied in drug-eluting stents to counteract restenosis, are natural products. Numerous studies show that natural products have proven to yield effective inhibitors of vascular smooth muscle cell proliferation and ongoing research effort might result in the discovery of further clinically relevant compounds. Many natural products have been so far tested regarding their potency to inhibit vascular smooth muscle cell proliferation, a process involved in atherosclerosis, pulmonary hypertension and restenosis. Compounds studied in vitro and in vivo as VSMC proliferation inhibitors include, for example indirubin-3'-monoxime, resveratrol, hyperoside, plumericin, pelargonidin, zerumbone and apamin. Moreover, taxol and rapamycin, the most prominent compounds applied in drug-eluting stents to counteract restenosis, are natural products. Numerous studies show that natural products have proven to yield effective inhibitors of vascular smooth muscle cell proliferation and ongoing research effort might result in the discovery of further clinically relevant compounds.Many natural products have been so far tested regarding their potency to inhibit vascular smooth muscle cell proliferation, a process involved in atherosclerosis, pulmonary hypertension and restenosis. Compounds studied in vitro and in vivo as VSMC proliferation inhibitors include, for example indirubin-3'-monoxime, resveratrol, hyperoside, plumericin, pelargonidin, zerumbone and apamin. Moreover, taxol and rapamycin, the most prominent compounds applied in drug-eluting stents to counteract restenosis, are natural products. Numerous studies show that natural products have proven to yield effective inhibitors of vascular smooth muscle cell proliferation and ongoing research effort might result in the discovery of further clinically relevant compounds. |
| Author | Wang, Dongdong Waltenberger, Birgit Horbańczuk, Jarosław Mihaly-Bison, Judit Tzvetkov, Nikolay T. Starzyński, Rafał R. Breuss, Johannes M. Atanasov, Atanas G. Uhrin, Pavel Mocan, Andrei Huminiecki, Łukasz Tewari, Devesh |
| Author_xml | – sequence: 1 givenname: Pavel orcidid: 0000-0002-9792-3420 surname: Uhrin fullname: Uhrin, Pavel email: pavel.uhrin@meduniwien.ac.at organization: Center for Physiology and Pharmacology, Institute of Vascular Biology and Thrombosis Research, Medical University of Vienna, Schwarzspanierstrasse 17, Vienna 1090, Austria – sequence: 2 givenname: Dongdong surname: Wang fullname: Wang, Dongdong organization: Department of Molecular Biology, Institute of Genetics and Animal Breeding of the Polish Academy of Sciences, ul. Postepu 36A, Magdalenka 05552, Poland – sequence: 3 givenname: Andrei surname: Mocan fullname: Mocan, Andrei organization: Department of Pharmaceutical Botany, "Iuliu Hatieganu" University of Medicine and Pharmacy, Strada Victor Babeş 8, Cluj-Napoca 400012, Romania – sequence: 4 givenname: Birgit surname: Waltenberger fullname: Waltenberger, Birgit organization: Institute of Pharmacy/Pharmacognosy, Center for Molecular Biosciences Innsbruck (CMBI), University of Innsbruck, Innrain 80-82, Innsbruck 6020, Austria – sequence: 5 givenname: Johannes M. surname: Breuss fullname: Breuss, Johannes M. organization: Center for Physiology and Pharmacology, Institute of Vascular Biology and Thrombosis Research, Medical University of Vienna, Schwarzspanierstrasse 17, Vienna 1090, Austria – sequence: 6 givenname: Devesh orcidid: 0000-0002-5125-3791 surname: Tewari fullname: Tewari, Devesh organization: Department of Pharmaceutical Sciences, Faculty of Technology, Kumaun University, Nainital, Uttarakhand 263136, India – sequence: 7 givenname: Judit surname: Mihaly-Bison fullname: Mihaly-Bison, Judit organization: Center for Physiology and Pharmacology, Institute of Vascular Biology and Thrombosis Research, Medical University of Vienna, Schwarzspanierstrasse 17, Vienna 1090, Austria – sequence: 8 givenname: Łukasz surname: Huminiecki fullname: Huminiecki, Łukasz organization: Department of Molecular Biology, Institute of Genetics and Animal Breeding of the Polish Academy of Sciences, ul. Postepu 36A, Magdalenka 05552, Poland – sequence: 9 givenname: Rafał R. surname: Starzyński fullname: Starzyński, Rafał R. organization: Department of Molecular Biology, Institute of Genetics and Animal Breeding of the Polish Academy of Sciences, ul. Postepu 36A, Magdalenka 05552, Poland – sequence: 10 givenname: Nikolay T. surname: Tzvetkov fullname: Tzvetkov, Nikolay T. organization: Pharmaceutical Institute, University of Bonn, An der Immenburg 4, Bonn 53121, Germany – sequence: 11 givenname: Jarosław surname: Horbańczuk fullname: Horbańczuk, Jarosław organization: Department of Molecular Biology, Institute of Genetics and Animal Breeding of the Polish Academy of Sciences, ul. Postepu 36A, Magdalenka 05552, Poland – sequence: 12 givenname: Atanas G. surname: Atanasov fullname: Atanasov, Atanas G. email: atanas.atanasov@univie.ac.at organization: Department of Molecular Biology, Institute of Genetics and Animal Breeding of the Polish Academy of Sciences, ul. Postepu 36A, Magdalenka 05552, Poland |
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| Keywords | Restenosis Molecular target Signaling pathway Drug-discovery Natural products Atherosclerosis Vascular smooth muscle cell proliferation |
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| SubjectTerms | Atherosclerosis Cancer Cell growth cell proliferation Drug-discovery Hypertension Inhibitors Molecular target Muscles Natural products paclitaxel pelargonidin Rapamycin Restenosis resveratrol Signaling pathway smooth muscle Taxol therapeutics Vascular endothelial growth factor Vascular smooth muscle cell proliferation |
| Title | Vascular smooth muscle cell proliferation as a therapeutic target. Part 2: Natural products inhibiting proliferation |
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