Genome Biology Lab, Department of Biosciences, Jamia Millia Islamia, Maulana Mohammad Ali Jauhar Marg, New Delhi 110025, India.
J Cancer Res Clin Oncol. 2011 Aug;137(8):1255-62. doi: 10.1007/s00432-011-0994-0. Epub 2011 Jun 23.
PTEN, a tumor-suppressor gene located on chromosome 10q23.3 is implicated in multiple tumors including cervical carcinoma.
We examined 135 cervical cancer specimens for PTEN gene expression and promoter methylation using methylation-specific PCR and immunohistochemistry and also studied the mutation in PTEN gene through PCR-single-stranded conformational polymorphism. PTEN expression and its methylation status were also correlated with clinicopathologic parameters.
The results showed an abnormal band on exon 5 and exon 9 of the PTEN gene. In PTEN gene, 61% specimen showed methylation. PTEN methylation was found in 39% cases of stage I, 60% of stage II, and 75% of stages III-IV. The correlation between PTEN methylation and clinical stage was found to be statistically significant (P = 0.003). Nuclear PTEN expression was detected in 84 of 135 (62%) cases of cervical carcinoma, and the remaining 51 of 135 (38%) cases were observed as expressional loss. The loss of PTEN expression was significantly correlated clinical stage (P = 0.001). Loss of PTEN expression was observed in 34 (41%) cases among 83 methylation positive cases, whereas among 52 methylation-negative cases, only 13 (25%) cases were seen as immunostaining negative with the statistically significant value (P = 0.05).
Promoter methylation and loss of PTEN expression occur frequently in carcinoma of uterine cervix. Our results suggest that PTEN plays an important role in the carcinogenesis of cervical cancer.
PTEN 是位于染色体 10q23.3 上的肿瘤抑制基因,与包括宫颈癌在内的多种肿瘤有关。
我们使用甲基化特异性 PCR 和免疫组织化学检查了 135 例宫颈癌标本中的 PTEN 基因表达和启动子甲基化情况,并通过 PCR-单链构象多态性研究了 PTEN 基因突变。还将 PTEN 表达及其甲基化状态与临床病理参数相关联。
结果显示,PTEN 基因的外显子 5 和外显子 9 出现异常带。在 PTEN 基因中,61%的标本显示甲基化。PTEN 甲基化在 I 期的 39%、II 期的 60%和 III-IV 期的 75%中发现。PTEN 甲基化与临床分期之间的相关性具有统计学意义(P=0.003)。在 135 例宫颈癌中,有 84 例(62%)检测到核 PTEN 表达,而其余 51 例(38%)观察到表达缺失。PTEN 表达缺失与临床分期显著相关(P=0.001)。在 83 例甲基化阳性病例中,有 34 例(41%)观察到 PTEN 表达缺失,而在 52 例甲基化阴性病例中,只有 13 例(25%)观察到免疫染色阴性,差异具有统计学意义(P=0.05)。
启动子甲基化和 PTEN 表达缺失在子宫颈癌中频繁发生。我们的结果表明,PTEN 在宫颈癌的发生中起重要作用。