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抑癌基因PTEN及其在肿瘤中的突变失活 被引量:3

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摘要 正常细胞和肿瘤细胞的蛋白质磷酸化及去磷酸化研究一直引人注目。研究表明,细胞内蛋白质酪氨酸磷酸化水平受蛋白质酪氨酸激酶和蛋白质酪氨酸磷酸酶动态调控。多种癌基因的表达产物具有蛋白质酪氨酸激酶活性并参与肿瘤形成进程,提示蛋白质磷酸酪氨酸磷酸酶可能抑制肿瘤形...
出处 《生命的化学》 CAS CSCD 1999年第2期95-97,共3页 Chemistry of Life
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参考文献4

  • 1Wang S I,Clin Cancer Res,1998年,4卷,811页
  • 2Li D M,Cancer Res,1997年,57卷,2124页
  • 3Li L W,J Biol Chem,1997年,272卷,29403页
  • 4Li J,Science,1997年,275卷,1943页

同被引文献14

  • 1[2]Steck PA, Pershouse MA, Jasser SA, et al. Indentification of a candidate tumor suppressor gene MMAC1 at chromosome 10q23.3 that is mutated in multiple advanced cancers. Nat Genet, 1997,15:356
  • 2[3]Lee JO ,Yang H, Georgescu MM, et al. Crystal structure of the PTEN tumor suppressor: implications for its phosphoinositide phosphatase activity and membrane association. Cell, 1999,99:323
  • 3[4]Rizo J, Sudhor TC. C2-domains, structure and function of a universal Ca2+-binging domain. J Biol Chem, 1998,273:15879
  • 4[5]Georgescu MM. The tumor suppressor activity of PTEN is regulated by its carboxyl-terminal region. Proc Natl Acad Sci USA, 1999,96:10182
  • 5[6]Tolkacheva T, Chan AML. Inhibition of H-Ras tansformation by the PTEN/MMAC1/TEP1 tumor suppressor gene. Oncogene, 2000, 19:680
  • 6[7]Adey NB, Huang L, Ormonde PA, et al. Threonine phosphorylation of the MMAC1/PTEN PDZ binding domain both inhibits and stimulates PDZ binding. Cancer Res, 2000, 60:35
  • 7[8]Wu X, Dowbenko D, Spencer S, et al. Evidence for regulation of PTEN tumor suppressor by a membrane-localized multi-PDZdomain of MAG13, a novel membrane-associated guanylate kinase. Proc Natl Acad Sci USA, 2000, 97:4233
  • 8[9]Wu X. Innteraction of the tumor suppressor PTEN/MMAC. Biol Chem, 2000,275:21477
  • 9[10]Cantley LC. New insights into tumor suppression: PTEN suppresses tumor formatoin by restraining the phosphoinositide 3-kinase/Akt pathway. Proc Natl Acad Sci USA, 1999, 96:4240
  • 10[11]Toker A, Newton AC. Cellular signaling: pivoting around PDK-1. Cell, 2000, 103:185

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