Literature DB >> 22834829

CREG: a possible candidate for both prevention and treatment of proliferative vascular disease.

Y Li1, C-H Yan, S-H Li, Y-L Han.   

Abstract

Cellular repressor of E1A-stimulated genes (CREG), a novel cellular protein, was discovered in 1998. Accumulating evidence, mainly from our laboratory, has suggested that CREG plays critical roles in reducing neointimal hyperplasia, maintaining vascular homeostasis, and promoting endothelial restoration. The study of CREG has the potential to offer new insights into both prevention and treatment of proliferative vascular disease, and will help us understand the processes of vascular repair after injury. It will also contribute to the development of new therapeutic strategies and devices, such as anti-in-stent restenosis stents. The present review summarizes our research on the molecular identity of CREG, and reviews the biological activities of CREG in regulating cell differentiation, proliferation, migration, and apoptosis of vascular smooth muscle cells and endothelial cells.

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Year:  2012        PMID: 22834829     DOI: 10.2174/156652412803833526

Source DB:  PubMed          Journal:  Curr Mol Med        ISSN: 1566-5240            Impact factor:   2.222


  2 in total

1.  Nanoporous CREG-eluting stent attenuates in-stent neointimal formation in porcine coronary arteries.

Authors:  Jie Deng; Yaling Han; Mingyu Sun; Jie Tao; Chenghui Yan; Jian Kang; Shaohua Li
Journal:  PLoS One       Date:  2013-04-03       Impact factor: 3.240

2.  An intronic miRNA regulates expression of the human endothelial nitric oxide synthase gene and proliferation of endothelial cells by a mechanism related to the transcription factor SP-1.

Authors:  Limei Yan; Min Kang; Zhengqi Qin; Wenyu Zhang; Yumei Li; Hesheng Ou
Journal:  PLoS One       Date:  2013-08-05       Impact factor: 3.240

  2 in total

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