Literature DB >> 12831500

Targeting the cell cycle machinery for the treatment of cardiovascular disease.

Katrina A Bicknell1, Elizabeth L Surry, Gavin Brooks.   

Abstract

Cardiovascular disease represents a major clinical problem affecting a significant proportion of the world's population and remains the main cause of death in the UK. The majority of therapies currently available for the treatment of cardiovascular disease do not cure the problem but merely treat the symptoms. Furthermore, many cardioactive drugs have serious side effects and have narrow therapeutic windows that can limit their usefulness in the clinic. Thus, the development of more selective and highly effective therapeutic strategies that could cure specific cardiovascular diseases would be of enormous benefit both to the patient and to those countries where healthcare systems are responsible for an increasing number of patients. In this review, we discuss the evidence that suggests that targeting the cell cycle machinery in cardiovascular cells provides a novel strategy for the treatment of certain cardiovascular diseases. Those cell cycle molecules that are important for regulating terminal differentiation of cardiac myocytes and whether they can be targeted to reinitiate cell division and myocardial repair will be discussed as will the molecules that control vascular smooth muscle cell (VSMC) and endothelial cell proliferation in disorders such as atherosclerosis and restenosis. The main approaches currently used to target the cell cycle machinery in cardiovascular disease have employed gene therapy techniques. We will overview the different methods and routes of gene delivery to the cardiovascular system and describe possible future drug therapies for these disorders. Although the majority of the published data comes from animal studies, there are several instances where potential therapies have moved into the clinical setting with promising results.

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Year:  2003        PMID: 12831500     DOI: 10.1211/002235703765344487

Source DB:  PubMed          Journal:  J Pharm Pharmacol        ISSN: 0022-3573            Impact factor:   3.765


  10 in total

1.  Forced expression of the cyclin B1-CDC2 complex induces proliferation in adult rat cardiomyocytes.

Authors:  Katrina A Bicknell; Carmen H Coxon; Gavin Brooks
Journal:  Biochem J       Date:  2004-09-01       Impact factor: 3.857

2.  Knockdown of cyclin-dependent kinase inhibitors induces cardiomyocyte re-entry in the cell cycle.

Authors:  Valeria Di Stefano; Mauro Giacca; Maurizio C Capogrossi; Marco Crescenzi; Fabio Martelli
Journal:  J Biol Chem       Date:  2011-01-05       Impact factor: 5.157

3.  Rubiarbonone C inhibits platelet-derived growth factor-induced proliferation and migration of vascular smooth muscle cells through the focal adhesion kinase, MAPK and STAT3 Tyr705 signalling pathways.

Authors:  Hyun-Soo Park; Khong Trong Quan; Joo-Hui Han; Sang-Hyuk Jung; Do-Hyung Lee; Eunji Jo; Tae-Wan Lim; Kyung-Sun Heo; MinKyun Na; Chang-Seon Myung
Journal:  Br J Pharmacol       Date:  2017-09-22       Impact factor: 8.739

4.  Capacity for resolution of Ras-MAPK-initiated early pathogenic myocardial hypertrophy modeled in mice.

Authors:  Bih-Rong Wei; Philip L Martin; Shelley B Hoover; Elizabeth Spehalski; Mia Kumar; Mark J Hoenerhoff; Julian Rozenberg; Charles Vinson; R Mark Simpson
Journal:  Comp Med       Date:  2011-04       Impact factor: 0.982

5.  Suppression of low-density lipoprotein oxidation, vascular smooth muscle cell proliferation and migration by a herbal extract of Radix Astragali, Radix Codonopsis and Cortex Lycii.

Authors:  Judy Y Chan; Johnny C Koon; Ping-Chung Leung; Chun-Tao Che; Kwok-Pui Fung
Journal:  BMC Complement Altern Med       Date:  2011-04-22       Impact factor: 3.659

Review 6.  Nanoparticulate carriers for the treatment of coronary restenosis.

Authors:  Luis Brito; Mansoor Amiji
Journal:  Int J Nanomedicine       Date:  2007

Review 7.  Cardiomyocyte proliferation in zebrafish and mammals: lessons for human disease.

Authors:  Gianfranco Matrone; Carl S Tucker; Martin A Denvir
Journal:  Cell Mol Life Sci       Date:  2016-11-03       Impact factor: 9.261

Review 8.  Phosphorylation Modifications Regulating Cardiac Protein Quality Control Mechanisms.

Authors:  Sumita Mishra; Brittany L Dunkerly-Eyring; Gizem Keceli; Mark J Ranek
Journal:  Front Physiol       Date:  2020-11-12       Impact factor: 4.566

9.  Regulation of cell cycle and stress responses to hydrostatic pressure in fission yeast.

Authors:  Vinoj T George; Gavin Brooks; Timothy C Humphrey
Journal:  Mol Biol Cell       Date:  2007-08-15       Impact factor: 4.138

10.  The cytotoxic role of intermittent high glucose on apoptosis and cell viability in pancreatic beta cells.

Authors:  Zhen Zhang; Jing Li; Lei Yang; Rongping Chen; Rui Yang; Hua Zhang; Dehong Cai; Hong Chen
Journal:  J Diabetes Res       Date:  2014-03-17       Impact factor: 4.011

  10 in total

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