Promoter Methylation and Loss of Expression of PTEN Gene in Breast Cancer Patients from Saudi Population

Mohammad Alam, A. Jerah, J. Ashraf, K. Kumaresan, Z. Eisa, N. Mikhail
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引用次数: 11

Abstract

Objective: PTEN, a tumor-suppressor gene, located on chromosome 10q23.3, is implicated in various types of cancer including breast cancer. The aim of this study is to investigate the promoter methylation, loss of expression and significance of PTEN gene in breast cancer and to determine the correlation between promoter methylation and gene expression. Methods: Promoter methylation and loss of expression of PTEN gene were analyzed using methylation-specific PCR and immunohistochemical methods respectively. The chi square test is used to correlate the promoter methylation and gene expression with their clincopathologic parameters. Results: We examined 53 breast cancer specimens and 10 normal tissues adjacent to tumor. The results showed a 58.5% promoter methylation in PTEN gene and none in normal tissue. PTEN methylation was observed in advanced stages III-IV (81.8%, 18 of 22, P=0.015) and higher grades G2-G3 (71.4%, 20 of 28, P=0.043) of disease. The correlation of PTEN methylation with clinical stage and tumor grade was found to be statistically significant. Nuclear PTEN expression was detected in 73.6% (39 of 53) cases of breast cancer and in the remaining 26.4% (14 of 53) cases expressional loss was observed. The loss of PTEN expression was observed in all normal tissues (10 of 10). The loss of PTEN expression was significantly correlated with patient’s age (P=0.028) and clinical stage (P = 0.029). The expressional loss was observed in 12 (38.7%) cases among 31 methylation positive cases, whereas among 22 methylation- negative cases, only 2 (9.1%) cases were seen as immunostaining negative with the statistically significant value (P=0.016). Conclusion: Promoter methylation and loss of expression of PTEN gene occur frequently in breast cancer. Our results suggest that PTEN plays an important role in breast carcinogenesis.
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沙特人群乳腺癌症患者PTEN基因启动子甲基化和表达缺失
目的:PTEN是一种肿瘤抑制基因,位于染色体10q23.3上,与包括乳腺癌在内的多种类型的癌症有关。本研究旨在探讨乳腺癌启动子甲基化、PTEN基因表达缺失及意义,确定启动子甲基化与基因表达的相关性。方法:分别采用甲基化特异性PCR和免疫组织化学方法分析启动子甲基化和PTEN基因表达缺失情况。卡方检验用于将启动子甲基化和基因表达与其临床病理参数相关联。结果:我们检查了53例乳腺癌标本和10例正常癌旁组织。结果显示,PTEN基因启动子甲基化率为58.5%,而正常组织中没有甲基化。在晚期III-IV期(81.8%,22 / 18,P=0.015)和更高级别的G2-G3 (71.4%, 28 / 20, P=0.043)中观察到PTEN甲基化。PTEN甲基化与临床分期、肿瘤分级的相关性有统计学意义。73.6%(53例中的39例)乳腺癌患者检测到核PTEN表达,其余26.4%(53例中的14例)患者观察到表达缺失。在所有正常组织中均观察到PTEN表达缺失(10 / 10)。PTEN表达缺失与患者年龄(P=0.028)、临床分期(P= 0.029)相关。31例甲基化阳性患者中有12例(38.7%)出现表达缺失,而22例甲基化阴性患者中仅有2例(9.1%)出现免疫染色阴性,差异有统计学意义(P=0.016)。结论:启动子甲基化和PTEN基因表达缺失在乳腺癌中常见。我们的研究结果表明PTEN在乳腺癌发生中起重要作用。
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