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Decreased expression of DNA repair genes (XRCC1 and XPD/ERCC2) in colorectal cancer in Iranian patients

机译:伊朗患者大肠癌中DNA修复基因(XRCC1和XPD / ERCC2)的表达降低

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The aim of this study was to investigate the role of the XRCC1 and XPD/ERCC2in the susceptibility and in the progression of colorectal cancer (CRC) in Iranian patients. Epidemiological studies have shown a positive association between defective DNA repair capacity and CRC. The underlying mechanism of their involvement is not wellunderstood. In the present study, we have analyzed the relationship between CRC and the expressionof DNA repair genes namely X-ray repair cross-complementing group 1 (XRCC1) and xeroderma pigmentosum group D (XPD)in 70 formalin fixed and paraffin embedded tumor tissues as well as normal adjacent tissues. The relative expressionof XRCC1and XPDin the mentioned tissues was performed for first time by quantitative real-time PCR (q-PCR). Results of this study demonstrated that difference of mean relative expressionbetween tumor tissues and normal tissues is 64-fold(XRCC1) > 16-fold(XPD). In multivariate logistic regression analysis, low expressionof XRCC1and XPDwas associated with a statistically significant increased risk of CRC [crude odds ratios (ORs) (95%CI) OR 2.10; (1.06-4.17) and OR 5.24 (2.38-11.52), respectively]. In conclusion, our study demonstrated that reduced expressionof XRCC1and XPDis associated with more than twofold increased risk in CRC
机译:这项研究的目的是调查XRCC1和XPD / ERCC2在伊朗患者的大肠癌易感性和进展中的作用。流行病学研究表明缺陷DNA修复能力与CRC之间存在正相关。他们参与的潜在机制还没有被很好地理解。在本研究中,我们分析了70个福尔马林固定和石蜡包埋的肿瘤组织中CRC与DNA修复基因表达的关系,即X射线修复交叉互补组1(XRCC1)和干性皮肤色素D组(XPD)。作为正常的邻近组织。 XRCC1和XPD在上述组织中的相对表达是通过定量实时PCR(q-PCR)进行的。研究结果表明,肿瘤组织与正常组织的平均相对表达差异为64倍(XRCC1)> 16倍(XPD)。在多元逻辑回归分析中,XRCC1和XPD的低表达与CRC的统计学上显着增加相关[原始几率(OR)(95%CI)OR 2.10; (1.06-4.17)和OR 5.24(2.38-11.52)]。总之,我们的研究表明XRCC1和XPDis的表达降低与CRC风险增加两倍以上有关

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