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首页> 外文期刊>DNA and Cell Biology >Specific 50'CpG island methylation signatures of FHIT and p16 genes and their potential diagnostic relevance in Indian breast cancer patients.
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Specific 50'CpG island methylation signatures of FHIT and p16 genes and their potential diagnostic relevance in Indian breast cancer patients.

机译:FHIT和P16基因的特异性50'CPG岛甲基化签名及其印度乳腺癌患者的潜在诊断相关性。

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摘要

Even after tremendous molecular studies, early detection,more accurate and sensitive diagnosis, and prognosis of breast cancer appear to be a riddle so far. To stab the enigma, this study is designed to envisage DNA methylation signatures as cancer-specific and stage-specific biomarkers in Indian patients. Rigorous review of scattered scientific reports on aberrant DNA methylation helped us to select and analyze a potential tumor suppressor gene pair (FHIT and p16 genes) in breast cancer patients. Methylation signatures from 232 primary sporadic breast cancer patients were pinpointed by methylation-specific PCR (MSP). To increase the sensitivity, we combined both MSP and expression studies (RT-PCR and Northern blotting) in a reproducible manner. Statistical analysis illustrated that hypermethylation of FHIT gene ( p < 0.0001) and p16 gene ( p=0.04) may be used as a potential diagnostic marker to diagnose the early and locally advanced stages of breast cancer. Additionally, the study authenticates the dependency of methylation and expressional loss of p16 gene on FHIT gene silencing. This observation not only describes the severity of disease when both genes are silenced but also drives to speculate the molecular cross talk between two genes or genetic pathways dictated by them separately.
机译:即使在巨大的分子研究之后,早期检测,更准确和敏感的诊断,迄今为止患者的乳腺癌预后似乎是谜语。为了刺伤谜,本研究旨在将DNA甲基化签名设想作为印度患者的癌症特异性和阶段特异性生物标志物。对异常DNA甲基化的分散科学报告的严格审查有助于我们在乳腺癌患者中选择和分析潜在的肿瘤抑制基因对(FHIT和P16基因)。来自232名主要孢子乳腺癌患者的甲基化签名通过甲基化特异性PCR(MSP)定位。为了提高敏感性,我们将MSP和表达研究(RT-PCR和Northern印迹)以可重复的方式组合。统计分析说明了FHIT基因的高甲基化(P <0.0001)和P16基因(P = 0.04)可以用作潜在的诊断标志物,以诊断乳腺癌的早期和局部晚期阶段。另外,该研究验证了对FHIT基因沉默的甲基化和表达损失的依赖性。这种观察不仅描述了两种基因沉默时疾病的严重程度,而且还驱动到分别由它们决定的两个基因或遗传途径之间的分子交叉谈话。

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