Literature DB >> 11208244

Gene therapy for restenosis after balloon angioplasty and stenting.

C Indolfi1, C Coppola, D Torella, O Arcucci, M Chiariello.   

Abstract

Percutaneous coronary revascularization is an increasingly attractive alternative to medical therapy and surgical revascularization for coronary artery disease. The leading drawback of this procedure continues to be restenosis-the process of late arterial renarrowing at the site of initially successful intervention. Restenosis after balloon angioplasty seems to be determined primarily by the direction and magnitude of vessel wall remodeling. In contrast, the major limitation of stent implantation is the initiation of neointimal tissue proliferation within and adjacent to the stent. The goal of this review is to summarize recent laboratory and clinical investigations of the transmission of mitogenic signals from the membrane to the nucleus in smooth muscle cells. The mechanisms responsible for restenosis after balloon angioplasty and stenting and the possibility of transferring specific genes into somatic vascular cells with molecular tools to inhibit smooth muscle cell proliferation also will be reviewed.

Entities:  

Mesh:

Year:  1999        PMID: 11208244     DOI: 10.1097/00045415-199911000-00010

Source DB:  PubMed          Journal:  Cardiol Rev        ISSN: 1061-5377            Impact factor:   2.644


  14 in total

Review 1.  Science, medicine, and the future: Genetics and cardiovascular risk.

Authors:  I N Day; D I Wilson
Journal:  BMJ       Date:  2001-12-15

Review 2.  Current understanding of coronary in-stent restenosis. Pathophysiology, clinical presentation, diagnostic work-up, and management.

Authors:  T M Schiele
Journal:  Z Kardiol       Date:  2005-11

3.  Cytocompatibility studies of an in situ photopolymerized thermoresponsive hydrogel nanoparticle system using human aortic smooth muscle cells.

Authors:  Abhimanyu Sabnis; Maham Rahimi; Christopher Chapman; Kytai T Nguyen
Journal:  J Biomed Mater Res A       Date:  2009-10       Impact factor: 4.396

4.  Exploring the molecular mechanisms of OSU-03012 on vascular smooth muscle cell proliferation.

Authors:  Wei-Wen Kuo; Jing-Ru Weng; Chih-Yang Huang; Chang-Hai Tsai; Wei-Hung Liu; Cheng-Hao Wen; Shih-Chang Tsai; Chieh-Hsi Wu
Journal:  Mol Cell Biochem       Date:  2010-07-13       Impact factor: 3.396

5.  In vivo near-infrared fluorescence imaging of integrin alphavbeta3 in an orthotopic glioblastoma model.

Authors:  Andrew R Hsu; Lewis C Hou; Anand Veeravagu; Joan M Greve; Hannes Vogel; Victor Tse; Xiaoyuan Chen
Journal:  Mol Imaging Biol       Date:  2006 Nov-Dec       Impact factor: 3.484

6.  Anti-Restenotic Roles of Dihydroaustrasulfone Alcohol Involved in Inhibiting PDGF-BB-Stimulated Proliferation and Migration of Vascular Smooth Muscle Cells.

Authors:  Pei-Chuan Li; Ming-Jyh Sheu; Wei-Fen Ma; Chun-Hsu Pan; Jyh-Horng Sheu; Chieh-Hsi Wu
Journal:  Mar Drugs       Date:  2015-05-15       Impact factor: 5.118

7.  Factorial analyses of photopolymerizable thermoresponsive composite hydrogels for protein delivery.

Authors:  Abhimanyu Sabnis; Aniket S Wadajkar; Pranesh Aswath; Kytai T Nguyen
Journal:  Nanomedicine       Date:  2009-02-11       Impact factor: 5.307

8.  Paeonia lactiflora Extract Attenuating Cerebral Ischemia and Arterial Intimal Hyperplasia Is Mediated by Paeoniflorin via Modulation of VSMC Migration and Ras/MEK/ERK Signaling Pathway.

Authors:  Yuh-Fung Chen; Kuo-Jen Wu; W Gibson Wood
Journal:  Evid Based Complement Alternat Med       Date:  2013-06-02       Impact factor: 2.629

9.  A Chinese herbal formula "Gan-Lu-Yin" suppresses vascular smooth muscle cell migration by inhibiting matrix metalloproteinase-2/9 through the PI3K/AKT and ERK signaling pathways.

Authors:  Yi-Chung Chien; Ming-Jyh Sheu; Chieh-Hsi Wu; Wen-Hsin Lin; Ying-Yi Chen; Po-Liang Cheng; Hsu-Chen Cheng
Journal:  BMC Complement Altern Med       Date:  2012-08-24       Impact factor: 3.659

10.  Pipoxolan ameliorates cerebral ischemia via inhibition of neuronal apoptosis and intimal hyperplasia through attenuation of VSMC migration and modulation of matrix metalloproteinase-2/9 and Ras/MEK/ERK signaling pathways.

Authors:  Yuh-Fung Chen; Huei-Yann Tsai; Kuo-Jen Wu; Lian-Ru Siao; W Gibson Wood
Journal:  PLoS One       Date:  2013-09-24       Impact factor: 3.240

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