Department of Radiation Biology, Korea Atomic Energy Research Institute, Yuseong, Daejeon 305-600, Republic of Korea.
Biochem Biophys Res Commun. 2010 Feb 12;392(3):448-53. doi: 10.1016/j.bbrc.2010.01.045. Epub 2010 Jan 15.
TSPYL5, encoding testis-specific Y-like protein, has been postulated to be a tumor suppressor gene, and its hypermethylation is often associated with human disease, especially cancer. In this study, we report that the TSPYL5 gene was less methylated (30%) in A549 lung adenocarcinoma cells, which are relatively resistant to gamma-radiation, than in H460 lung cancer cells, in which the TSPYL5 gene was hypermethylated (95%); thus, the expression level of TSPYL5 is much higher in A549 cells than in H460 cells. We showed that TSPYL5 suppression with silencing RNA in A549 cells up-regulated cellular PTEN, followed by down-regulation of AKT activation. Therefore, blockage of TSPYL5 sensitized A549 cells to cytotoxic agents such as gamma-radiation. In addition, TSPYL5 suppression also showed an increased level of p21(WAF1/Cip1) and subsequently induced inhibition of cell growth in A549 cells. The overexpression of TSPYL5 in H460 cells showed the opposite effects. This study provides the first demonstration that TSPYL5 modulates cell growth and sensitization of cells to the detrimental effects of damaging agents via regulation of p21(WAF1/Cip1) and PTEN/AKT pathway.
TSPYL5 编码睾丸特异性 Y 样蛋白,被推测为一种肿瘤抑制基因,其超甲基化常与人类疾病,特别是癌症有关。在这项研究中,我们报告 TSPYL5 基因在 A549 肺腺癌细胞中甲基化程度较低(30%),而在 H460 肺癌细胞中甲基化程度较高(95%),因此 TSPYL5 在 A549 细胞中的表达水平远高于 H460 细胞。我们表明,在 A549 细胞中用沉默 RNA 抑制 TSPYL5 可上调细胞中的 PTEN,随后下调 AKT 的激活。因此,阻断 TSPYL5 可使 A549 细胞对细胞毒剂(如伽马射线)敏感。此外,TSPYL5 的抑制还显示出 p21(WAF1/Cip1)的水平增加,随后在 A549 细胞中抑制细胞生长。TSPYL5 在 H460 细胞中的过表达则显示出相反的效果。这项研究首次证明,TSPYL5 通过调节 p21(WAF1/Cip1)和 PTEN/AKT 通路,调节细胞生长并使细胞对损伤剂的有害作用敏感。