期刊文献+

P38 MAPK信号传导通路与卵巢癌关系的研究进展 被引量:2

Advances in Researches on the Relationship between P38 MAPK Signaling Pathway and Ovarian Carcinoma
原文传递
导出
摘要 丝裂原活化蛋白激酶(mitogen-activated proteinkinases,MAPKs)级联反应是细胞内重要的信号传导系统之一,参与细胞生长、发育、分化和凋亡等一系列生理、病理过程.P38 MAPK信号传导通路是MAPK通路的分支之一,介导了应激、炎性细胞因子、细菌产物等多种刺激引起的细胞反应,对细胞周期调控具有重要作用.但对不同的卵巢癌细胞系,或者不同的刺激,P38通路的作用不完全相同,甚至可能相反,提示对P38通路的功能仍需进一步的研究,他可能是肿瘤治疗的新靶点.本文就P38 MAPK信号传导通路与卵巢癌关系作一综述。 The cascade reaction of mitogen-activated protein kinases(MAPKs)is one of the vital intracellular signal transduction systems,participating in many physiological progressions,such as cell growth,proliferation,differentiation and apoptosis.P38 is a member of MAPKs,mediating many cell reactions induced by stress,inflammatory cytokines or bacterial products and playing a key role in the regulation of cell cycle.For different cell lines of ovarian carcinoma,P38 has different functions.The same phenomenon can be seen when the cells are presented under different stimulus.P38 pathway may be one candidate target of cancer therapy.This paper will review the relationship between P38MAPK signaling pathway and ovarian carcinoma.
出处 《现代生物医学进展》 CAS 2012年第4期780-783,共4页 Progress in Modern Biomedicine
关键词 丝裂原活化蛋白激酶 P38 卵巢癌 Mitogen-activated protein kinase P38 Ovarian carcinoma
  • 相关文献

参考文献37

  • 1Han J,Lee JD,Bibbs L,Ulevitch RJ.A MAP kinase targeted byendotoxin and hyperosmolarity in mammalian cells[J].Science,1994,265:808-811.
  • 2Jiang Y,Chen C,Li Z,Guo W,Gegner JA,Lin S,Han J.Characterizationof the structure and function of a new mitogen-activated proteinkinase(p38beta)[J].J Biol Chem,1996,271:17920-17926.
  • 3Li Z,Jiang Y,Ulevitch RJ,Han J.The primary structure of p38 gamma:anew member of p38 group of MAP kinases[J].Biochem Biophys ResCommun,1996,228:334-340.
  • 4Jiang Y,Gram H,Zhao M,New L,Gu J,Feng L,Di Padova F,Ulevitch RJ,Han J.Characterization of the structure and function ofthe fourth member of p38 group mitogen-activated protein kinases[J]Biol Chem,1997,272:30122-30128.
  • 5龚小卫,姜勇.丝裂原活化蛋白激酶(MAPK)生物学功能的结构基础[J].中国生物化学与分子生物学报,2003,19(1):5-11. 被引量:33
  • 6Sudo T,Yagasaki Y,Hama H,Watanabe N,Osada H.Exip,a newalternative splicing variant of p38 alpha,can induce an earlier onset ofapoptosis in HeLa cells[J].Biochem Biophys Res Commun,2002,291:838-843.
  • 7Enslen H,Raingeaud J,Davis RJ.Selective activation of p38mitogen-activated protein(MAP)kinase isoforms by the MAP kinasekinases MKK3 and MKK6[J].Biol Chem,1998,273:1741-1748.
  • 8Brunet A,Pouysségur J.Identification of MAP kinase domains byredirecting stress signals into growth factor responses[J].Science,1996,272:1652-1655.
  • 9Jiang Y,Li Z,Schwarz EM,Lin A,Guan K,Ulevitch RJ,Han J.Structure-function studies of p38 mitogen-activated protein kinase.Loop 12 influences substrate specificity and autophosphorylation,butnot upstream kinase selection[J].Biol Chem,1997,272:11096-11102.
  • 10Widmann C,Gibson S,Jarpe MB,Johnson GL.Mitogen-activated pro-tein kinase:conservation of a three-kinase module from yeast tohuman[J].Physiol.Rev,1999,79:143-180.

二级参考文献99

  • 1Tyler ZARUBIN.Activation and signaling of the p38 MAP kinase pathway[J].Cell Research,2005,15(1):11-18. 被引量:149
  • 2JingLIU AnningLIN.Role of JNK activation in apoptosis:Adouble-edged sword[J].Cell Research,2005,15(1):36-42. 被引量:75
  • 3李栢林,韩硕,李凤,韩艳春,宋敏,宋继谒.p38信号蛋白在乳腺癌组织中表达的研究[J].中国老年学杂志,2006,26(3):346-349. 被引量:6
  • 4Nigg E A.Mitotic kinases as regulators of cell division and its checkpoints[J].Nat Rev Mol Cell Biol,2001,2(1):21-32.
  • 5Pyerin W,Ackermann K.The genes encoding human protein kinase CK2 and their functional links[J].Prog Nucleic Acid Res Mol Biol,2003,74:239 -73.
  • 6Litchfield D W.Protein kinase CK2:structure,regulation and role in cellular decisions of life and death[J].Biochem J,2003,369(Pt 1):1 -15.
  • 7Pinna L A.The raison d'etre of constitutively active protein kinases:the lesson of CK2[J].Acc Chem Res,2003,36(6):378 -84.
  • 8Yde C W,Ermakova I,Issinger O G,et al.Inclining the purine base binding plane in protein kinase CK2 by exchanging the flanking side-chains generates a preference for ATP as a cosubstrate[J].J Mol Biol,2005,347(2):399 -414.
  • 9Ryu S W,Woo J H,Kim Y H,et al.Downregulation of protein kinase CK2 is associated with cellular senescence[J].FEBS Lett,2006,580 (3):988-94.
  • 10Meggio F,Pinna L A.One-thousand-and-one substrates of protein kinase CK2?[J].FASEB J,2003,17(3):349 -68.

共引文献119

同被引文献53

引证文献2

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