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首页> 外文期刊>Life sciences >Clinical significance of promoter hypermethylation of RASSF1A, RARbeta2, BRCA1 and HOXA5 in breast cancers of Indian patients.
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Clinical significance of promoter hypermethylation of RASSF1A, RARbeta2, BRCA1 and HOXA5 in breast cancers of Indian patients.

机译:印度患者乳腺癌中RASSF1A,RARbeta2,BRCA1和HOXA5启动子高甲基化的临床意义。

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摘要

Promoter hypermethylation of genes is implicated in the pathogenesis of many cancers, including breast cancer. Herein, we analyzed the promoter methylation status of a panel of critical growth regulatory genes, RASSF1A, RARbeta2, BRCA1 and HOXA5, in 54 breast cancers and 5 distant normal breast tissues of Indian patients. The methylation data were correlated with clinicopathological characteristics and hormone receptor status to determine the impact of methylation in breast carcinogenesis. Promoter hypermethylation of RASSF1A was observed in 39/54 (72%), HOXA5 in 36/54 (67%), BRCA1 in 15/54 (28%) and RARbeta2 in 8/54 (15%) breast cancers. Our most significant findings were the association of RASSF1A methylation with nodal metastasis (p=0.05); and RARbeta2 methylation with age (all tumors in patients in the older age group were methylated, p=0.04). Further, the interactions between DNA methylation and hormone receptor biology in breast cancer cells are beginning to be clearly understood. In this contextthe association of HOXA5 methylation with loss of ERalpha (p=0.009) is noteworthy.
机译:基因的启动子高甲基化与包括乳腺癌在内的许多癌症的发病机理有关。在这里,我们分析了一组关键生长调节基因RASSF1A,RARbeta2,BRCA1和HOXA5在54例乳腺癌和5例印度患者正常乳腺组织中的启动子甲基化状态。甲基化数据与临床病理特征和激素受体状态相关,以确定甲基化对乳腺癌致癌作用的影响。在39/54(72%),36/54(67%)的HOXA5、15 / 54(28%)的BRCA1和8/54(15%)的RARbeta2中观察到RASSF1A的启动子高甲基化。我们最重要的发现是RASSF1A甲基化与淋巴结转移相关(p = 0.05);和RARbeta2甲基化随年龄的增长(老年组患者的所有肿瘤均被甲基化,p = 0.04)。此外,开始清楚地了解乳腺癌细胞中DNA甲基化与激素受体生物学之间的相互作用。在这种情况下,HOXA5甲基化与ERalpha丢失的关联(p = 0.009)是值得注意的。

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