期刊文献+

抗肿瘤药物新靶点半胱天冬酶-10

下载PDF
导出
摘要 细胞凋亡过程是依赖天冬氨酸特异性的半胱氨酸蛋白酶(半胱天冬酶)产生的级联反应。半胱天冬酶-10是凋亡途径中关键的启动子,能够通过寡聚而自身切割活化,并能激活下游其他半胱天冬酶,参与细胞凋亡过程。半胱天冬酶-10基因突变及其它表达异常可导致细胞凋亡和增殖失调,从而参与某些肿瘤和免疫系统疾病的发生和发展。半胱天冬酶-10有可能是抗肿瘤药物的新靶点。
出处 《药学实践杂志》 CAS 2006年第2期76-79,共4页 Journal of Pharmaceutical Practice
  • 相关文献

参考文献24

  • 1Yuan J, Shaham S, Ledoux S, et al. The C. elegans cell death gene Ced-3 encodes a protein similar to mammalian interleukin-1 1β-converting enzyme[J]. Cell, 1993, 75 (4) : 641.
  • 2Xue D, Shaham S, Horvitz HR. The Caenorhabditis elegans celldeath protein CED-3 is a eysteine protease with substrate specificities similar to those of the human CPP32 protease [J]. Genes Dev, 1996, 10(9): 1073.
  • 3Shi, Y. Mechanisms of caspase inhibition and activation during apoptosis[J]. Mol. Cell, 2002, 9(3): 459.
  • 4Fernandes-Alnemri T, Armstrong RC, Kiths J, et al, In vitro activation of CPP32 and Mch3 by Mch4, a novel human apoptotic cysteine protease containing two FADD-like domains [J]. Proc Nail Acad Sci U S A, 1996, 93(15) : 7464.
  • 5Vincenz C, Dixit VM. Fas-assoeiated Death Domain Protein Interleukin-1 β-converting Enzyme 2 ( FLICE2 ), an ICE/Ced-3 Homologue, Is Proximally Involved in CD95- and p55-mediated Death Signaling[J]. J Biol Chem,1997 ,272(10) : 6578.
  • 6Ng PW, Porter AG, Janicke RU. Molecular Cloning and Characterization of Two Novel Pro-apoptotic Isoforms of caspase-10[J] ,J Biol Chem,1999, 274(15) : 10301.
  • 7Wang J, Chun HJ, Wang W, et al. caspase-10 is an initiator caspase in death receptor signaling[J]. Proc Natl Acad Sci U SA,2001,98 (24) :13884.
  • 8Kischkel FC, Lawrence DA, Tinel A, et al. Death receptor recruitment of endogenous caspase-10 and apoptosis initiation in theabsence of caspase -8[J]. J Biol Chem, 2001, 276(49):46639.
  • 9Harada K, Toyooka S, Shivapurkar N, et al. Deregulation of caspase-8 and -10 expression in pediatric tumors and cell lines[J]. Cancer Res, 2002, 62(20) : 5897.
  • 10Kisehkel FC, Lawrence DA, Chuntharapai A, et al. Apo2L/TRAIL-dependent recruitment of endogenous FADD and caspase-8 to death receptors 4 and 5[J]. Immunity, 2000,12(6):611.

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