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野生型PTEN转染对胶质母细胞瘤基因表达的影响 被引量:7

The effects of wild-type PTEN transfection on gene expressions of glioblastomas
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摘要 目的 研究野生型PTEN对胶质母细胞瘤基因表达的影响及意义。方法 用表达野生型PTEN的载体转染PTEN失活的胶质母细胞瘤细胞系U87MG ,筛选出稳定表达野生型PTEN的细胞克隆 ,然后用cDNA微阵列技术找出野生型PTEN转染后mRNA表达改变的基因。结果 转染的野生型PTEN可以明显抑制U87MG肿瘤细胞的增殖。用cDNA微阵列技术分析后 ,共有 89个cDNA克隆在PTEN转染细胞与对照组细胞之间差异有显著性 (P <0 .0 1)。其中 ,76个为已知基因 ,包括胶质纤维酸性蛋白、p2 1/WAF1、转化生长因子β诱导的早期蛋白、DNA碎裂因子 4 5等 ;13个为未知基因。 结论 野生型PTEN可以影响多种基因的表达 ,从而调控胶质母细胞瘤细胞的增殖、分化。 Objective To study the effects of wild type PTEN on gene expressions of glioblastomas. Methods Glioblastoma U87MG cells, which express inactivated PTEN, were transfected with wild type PTEN constructs and stable transfected clones were selected. Then, cDNA microarray analyses were used to identify differentially expressed genes in wild type PTEN transfected cells and control cells. Results Transfected wild type PTEN inhibited the proliferation of U87MG. By cDNA microarray analyses, 89 cDNA clones were identified, which were differentially expressed in wild type PTEN transfected cells and control cells. Among these genes, 13 genes were unknown and 76 genes were known genes, including glial fibrillary acidic protein, p21/WAF1, human TGF β inducible early protein, human DNA fragmentation factor 45 etc. Conclusion Wild type PTEN can affect the expressions of multiple genes, by which it regulates the proliferation, differentiation and apoptosis of glioblastomas.
出处 《中华病理学杂志》 CAS CSCD 北大核心 2002年第1期46-49,共4页 Chinese Journal of Pathology
基金 美国中华医学会基金 (CMB)专项人才项目资助(2 0 0 0 0 61)
关键词 胶质母细胞瘤 基因转染 抑制基因 野生型PTEN 基因表达 影响 Glioblastoma Transfection Genes,suppressor, tumor PTEN
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  • 1Li J, Yen C, Liaw D, et al. PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer. Science, 1997, 275: 1943-1947.
  • 2Wu RC,Li X,Schonthal AH. Transcriptional activation of p21/WAF1 by PTEN/MMAC1 tumor suppressor. Mol Cell Biochem,2000, 203: 59-71.
  • 3Myers MP, Stolarov JP, Eng C, et al. P-TEN, the tumor suppressor from human chromosome 10q23, is a dual-specificity phosphatase. Proc Natl Acad Sci U S A, 1997, 94: 9052-9057.
  • 4Tian XX, Pang JC, To SS, et al. Restoration of wild-type PTEN expression leads to apoptosis, induces differentiation, and reduces telomerase activity in human glioma cells. J Neuropathol Exp Neurol,1999, 58: 472-479.
  • 5何志巍,姚开泰.DNA微阵列(或芯片)技术原理及应用[J].生物化学与生物物理进展,1999,26(5):507-510. 被引量:20
  • 6李志强,袁先厚.PTEN基因与脑胶质瘤[J].国外医学(遗传学分册),2000,23(3):150-152. 被引量:5
  • 7田新霞,吴浩强.新的肿瘤抑制基因PTEN[J].中华病理学杂志,2000,29(6):455-457. 被引量:14
  • 8Stambolic V, Suzuki A, dela Pompa JL, et al. Negative regulation of PKB/Akt-dependent cell survival by the tumor suppressor PTEN. Cell,1998, 95: 29-39.
  • 9Li DM, Sun H. TEP1, encoded by a candidate tumor suppressor locus, is a novel protein tyrosine phosphatase regulated by transforming growth factor β. Cancer Res,1997, 57: 2124-2129.

二级参考文献23

  • 1Wodicka L,Nature Biotechnol,1997年,15卷,13期,1359页
  • 2Heller R A,Proc Nat Acad Sci USA,1997年,94卷,2150页
  • 3Gress T M,Oncogene,1996年,13卷,1819页
  • 4Lee M,Science,1996年,274卷,610页
  • 5Tian X X,J Neuropathol Exp Neurol,1999年,58卷,472页
  • 6Furnari F B,Cancer Res,1998年,58卷,5002页
  • 7Gu J,J Cell Biol,1998年,143卷,1375页
  • 8Tamura M,Science,1998年,280卷,1614页
  • 9Li D M,Cancer Res,1997年,57卷,2124页
  • 10Li J,Science,1997年,275卷,1943页

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