期刊文献+

miRNAs与细胞衰老相关的信号通路 被引量:4

The Role of miRNAs in Aging-related Signaling Pathways
下载PDF
导出
摘要 miRNAs是一类负调控基因表达的内源性非编码小分子RNA,在细胞衰老过程中发挥重要作用.细胞衰老是指可增殖细胞在各种应激下出现细胞周期阻滞,并且丧失增殖能力,进入一种不可逆的、相对稳定的状态.p53、p21、p16、SIRT1、胰岛素/IGF-1及mTOR等蛋白是衰老相关信号通路中的重要分子,参与细胞衰老过程.研究表明,miRNAs可以通过调控这些衰老相关蛋白所在的信号通路,促进或延缓细胞衰老.本文综述细胞衰老相关的miRNAs,以及它们对衰老相关信号通路的影响,为深化认识衰老和衰老相关疾病的分子机制奠定基础. MicroRNAs (miRNAs) are small endogenous noncoding RNA molecutes that are aBle to repress gene expression, and are known to play essential roles in the controlling of cellular senescence. Cellular senescence is represented by the irreversible proliferation arrest in response to various types of stress. The aging-related signaling pathways involving p53, p21 , p16, SIRT1 , insulin/IGF-1 and mTOR have been shown to be important in recent reports, where the miRNAs could either promote or delay cellular senescence through regulating the aging-related signaling proteins. Here we reviewed the reported aging-related miRNAs with their roles on the signaling pathways in cellular senescence.
出处 《中国生物化学与分子生物学报》 CAS CSCD 北大核心 2013年第5期412-418,共7页 Chinese Journal of Biochemistry and Molecular Biology
基金 国家自然科学基金(No.30672205 30871440 30971620 81000143 81170327) 广东省自然科学基金(No.S2012010008219 9252402301000002 S2011010002922 8452402301001450) 东莞市科技计划重点项目(No.2011105102007) 广东省医学科研基金项目(No.A2011431) 广东医学院科技创新基金(No.STIF201102)~~
关键词 MIRNAS 信号通路 细胞衰老 miRNAs signaling pathways cellular senescence
  • 相关文献

参考文献53

  • 1Peters L, Meister G. Argonaute proteins: mediators of RNA silencing [ J ]. Mol Cell, 2007,26 ( 5 ) : 611-623.
  • 2Pillai RS,Bhattacharyya SN,Filipowicz W. Repression of protein synthesis by miRNAs: how many mechanisms? [ J]. Trends Cell Bio1,2007,17 (3) : 118-126.
  • 3Martinez I,Almstead L L, DiMaio D. MicroRNAs and senescence [J]. Aging (Albany NY) ,2011,3(2) :77-78.
  • 4Feng Z, Zhang C, Wu R, et al. Tumor suppressor p53 meets microRNAs[ J]. J Mol Cell Biol,2011,3( 1 ) :44-50.
  • 5Chang T C, Wentzel E A, Kentl O A, et al. Transactivation of miR-34a by p53 broadly influences gene expression and promotes apoptosis [ J]. Mol Cell ,2007,26( 5 ) :745-752.
  • 6Tazawa H, Tsuchiya N, Izumiya M, et al. Tumor-suppressive miR- 34a induces senescence-like growth arrest through modulation of the E2F pathway in human colon cancer ceils[ J]. Proc Natl Acad Sci U S A,2007, 104(39) :15472-15477.
  • 7He L, He X Y, Lim L P, et al. A microRNA component of the p53 tumour suppressor network [ J ]. Nature, 2007, 447 ( 7148 ) : 1130-1134.
  • 8Sachdeva M, Zhu S M, Wu F T, et al. p53 represses c-Myc through induction of the tumor suppressor miR-145 [ J]. Proc Natl Acad Sci U S A,2009,106(9) :3207-3212.
  • 9Georges S A,Bieryet M C, Kim S Y,et al. Coordinated regulation of cell cycle transcripts by p53-inducible microRNAs, miR-192 and miR-215 [ J ]. Cancer Res,2008,68 (24) : 10105-10112.
  • 10Tian S, Huang S, Wu S, et al. MicroRNA-1285 inhibits the expression of p53 by directly targeting its 3" untranslated region [J]. Biochem Biophys Res Commun,2010,396(2) :435-439.

同被引文献82

  • 1胡作为,沈自尹,黄建华.淫羊藿总黄酮保护衰老细胞端粒长度缩短的实验研究[J].中国中西医结合杂志,2004,24(12):1094-1097. 被引量:28
  • 2江艳,王浩,吕龙,田庚元.灵芝孢子粉多糖Lzps-1的化学研究及其总多糖的抗肿瘤活性[J].药学学报,2005,40(4):347-350. 被引量:31
  • 3沈自尹,袁春燕,黄建华,郭爱克,胡作为.淫羊藿总黄酮延长果蝇寿命及其分子机制[J].中国老年学杂志,2005,25(9):1061-1063. 被引量:17
  • 4王芳,余佳,张俊武.小RNA(MicroRNA)研究方法[J].中国生物化学与分子生物学报,2006,22(10):772-779. 被引量:14
  • 5Keene J D. RNA regulons: coordination of post-transcriptionalevents[ J]. Nat Rev Genet, 2007 , 8(7) :533-543.
  • 6Srouji S,Livne E. Bone marrow stem cells and biological scaffoldfor bone repair in aging and disease [ J ]. Mech Ageing Dev,2005,126(2) : 281-287.
  • 7Song L, Tuan RS. MicroRNAs and cell differentiation inmammalian development [ J ]. Birth Defects Res C EmbryoToday,2006,78(2) : 140-149.
  • 8Oskowitz A Z, Lu J, Penfomis P, et al. Human multipotentstromal cells from bone marrow and microRNA : regulation ofdifferentiation and leukemia inhibitory factor expression[ J]. ProcNatl Acad Sci USA,2008 ,105(47) :18372-18377.
  • 9Mizuno, Y Tokuzawa, Y Ninomiya, et al. miR-210 promotesosteoblastic differentiation through inhibition of AcvRlb [ J ].FEBS Lett,2009,583(9) :2263-2368.
  • 10Baek W Y, Kim J E. Transcriptional regulation of bone formation[J]. Front Biosci Sch Ed, 2011,3(7) :126-135.

引证文献4

二级引证文献12

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