Department of Internal Medicine-Oncology, The First Affiliated Hospital, Zhengzhou University, Zhengzhou, China.
Dig Dis Sci. 2010 Aug;55(8):2219-26. doi: 10.1007/s10620-009-0992-0. Epub 2009 Oct 3.
Human TIP30 was initially identified as a candidate metastasis suppressor gene whose expression was down-regulated in human liver, lung, breast, and prostate cancers, and recently the role of this gene was examined in colorectal cancer. The aim of this study was to determine the level of TIP30 expression in colorectal carcinoma (CRC).
TIP30 protein levels were lower in colorectal carcinomas compared to normal tissue from the control group (P < 0.001). The frequencies of hypermethylation of TIP30 in tumor were 36%, while there was no aberrant methylation in paired adjacent non-tumor tissue. A statistically significant inverse association was found between TIP30 methylation status and expression of the TIP30 protein in tumor tissues (P = 0.006). Somatic missense mutations in the TIP30 gene were identified in human CRC tissue specimens.
Our results demonstrate that promoter methylation is involved in the decreased expression of TIP30 tumor suppressor gene in human colorectal carcinoma.
人类 TIP30 最初被鉴定为候选转移抑制基因,其在人类肝癌、肺癌、乳腺癌和前列腺癌中的表达下调,最近该基因在结直肠癌中的作用也被研究。本研究旨在确定 TIP30 在结直肠癌中的表达水平。
与对照组正常组织相比,结直肠癌组织中 TIP30 蛋白水平较低(P<0.001)。肿瘤中 TIP30 异常甲基化的频率为 36%,而配对的相邻非肿瘤组织中则没有异常甲基化。在肿瘤组织中,TIP30 甲基化状态与 TIP30 蛋白表达之间存在统计学显著的负相关(P=0.006)。在人类 CRC 组织标本中鉴定到 TIP30 基因的体细胞错义突变。
我们的结果表明,启动子甲基化参与了人类结直肠癌中 TIP30 肿瘤抑制基因表达的下调。