期刊文献+

分泌型卷曲相关蛋白1在心血管疾病中的研究进展 被引量:2

Present state of research on sFRP-1 in relation to cardiovascular disease
下载PDF
导出
摘要 分泌型卷曲相关蛋白1(sFRP-1)基因实质为一种分泌型糖蛋白,主要与Wnt信号通路具有同源结构的卷曲蛋白受体竞争性结合,通过对Wnt信号通路的负调控,广泛介入到调控细胞增殖、分化、凋亡、癌变以及调节机体的生长发育、疾病等病理生理的复杂过程.抑制Wnt信号通路可以阻止心肌细胞缺血坏死面积的进一步扩大,延缓心肌重塑的过程,进而改善预后.作为Wnt信号通路的抑制因子,sFRP-1的作用不可忽视.相关实验研究结果表明,sFRP-1基因很有可能成为未来心血管疾病治疗的靶向基因. The sFRP-1 gene, in essence, is a secretory glycoprotein, which plays a negative regulatory role in the Wnt signaling pathway by competitively binding to frizzled protein receptors with homologous structures in the Wnt signaling pathway. By negatively regulating the Wnt signaling pathway, it is widely involved in the complex pathophysiological processes of regulating cell proliferation. differentiation, apoptosis, carcinogenesis, growth, development and disease of the body. Inhibition of Wnt signaling pathway can prevent further expansion of infarct area of myocardial cells, delay the process of myocardial remodeling and thereby improve the prognosis. As an inhibiting factor of Wnt signaling pathway, the role of sFRP-1 cannot be neglected and the results of related experimental studies show that sFRP-1 gene is likely to become a target gene for future cardiovascular disease treatment.
作者 印纹源(综述) 马依彤(审校) YIN Wen-yuan;MA Yi-tong(Heart Center,the First Affiliated Hospital of Xinjiang Medical University,Urumqi 830054,China)
出处 《中国心血管病研究》 CAS 2019年第4期300-304,共5页 Chinese Journal of Cardiovascular Research
基金 国家自然科学基金资助项目(81470468).
关键词 WNT信号通路 分泌型卷曲相关蛋白1 心肌梗死 Wnt signaling pathway sFRP-1 Myocardial infarction
  • 相关文献

参考文献2

二级参考文献30

  • 1Goliash G, Wiesbauer F, Graft A, et al. The effect of p22- PHOX (CYBA) polymorphisms on premature coronary artery dis- ease ( ≤40 years of age ). Thromb Haemost, 2011,105 : 529- 534.
  • 2Mani A, Radhakrishnan J, Wang H, et al. LRP6 mutation in a family with early coronary disease and metabolic risk factors. Sci- ence, 2007,315 : 1278-1282.
  • 3Castelo-Branco G, Wagner J, Rodrignez FJ, et al. Differential regulation of midbrain dopaminergic neurou development by Wnt- 1, Wnt-3a, and Wnt-5a. Pro Natl Acad Sci USA,2003,100: 12747 - 12752.
  • 4Naito AT, Shiojima I, Akazawa H, et al. Developmental stage- specific biphasic roles of Wnt/beta-catenin signling in cardiomyo- genesis and hematopoiesis. Proc Acad Sci ,2006,103 : 19812 - 19817.
  • 5Laframboise WA, Bombach KL, Dhir R J, et al. Molecular dy- namics of the compensatory response to myocardial infarct. J Mol Cell Cardiol, 2005,38 : 103-117.
  • 6Scott JJ, Mohlke KL, Bonnycastle LL, et al. A genome-wide as- sociation study of type 2 diabetes in Finns detects multiple sus- ceptibility variants. Science, 2007,316 : 1341-1345.
  • 7Abiola M, Favier M, Christodoulou-Vafeiadou E, et al. Activa- tion of Wnt/beta-catenin signaling increases insulin sensitivity through a reciprocal regulation of Wntl0b and SREBP-lc skele- tal muscle cells. Plos One, 2009,4 : e8509.
  • 8Wright WS, Longo KA, Dolinsky VW, et al. WntlOb inhibits obesity in ob/ob and agouti mice. Diabetes, 2007,56:295-303.
  • 9Fujino T, Asaba H, Kang MJ, et al. Low-density lipoprotein receptor-related protein 5 (LRPS) is essential for normal cholesterol metabolism and glucose-induced insulin secretion. Proc Natl Acad Sci USA,2003,100:229-234.
  • 10Magoori K, Kang MJ, ho MR, et al. Severe hypercholes- terolemia, impaired fat tolerance, and advanced atherosclerosis in mice lacking both low density lipoprotein receptor-related protein 5 and apolipoprotein E. J Biol Chem,2003,278:11331-11336.

共引文献6

同被引文献16

引证文献2

二级引证文献14

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部