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首页> 外文期刊>Nucleosides, nucleotides and nucleic acids >A genetic variant in the flanking region of miR-182 could decrease the susceptibility to the breast cancer risk in the iranian population
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A genetic variant in the flanking region of miR-182 could decrease the susceptibility to the breast cancer risk in the iranian population

机译:miR-182侧翼区域的遗传变异可以降低伊朗人群对乳腺癌风险的易感性

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Breast cancer is one of the most malignant tumors in the world. It is, in fact, the second leading cause of cancer death in women. Recent research has identified the role of miR-182 in this disease as an oncogene agent. In this study, the association of rs4541843 in the flanking region of the miR-182 sequence with the susceptibility to breast cancer risk has been studied in the Iranian population. By using the PCR_RFLP, the genotype rs4541843 was determined in 161 patients and 164 control subjects. The genotypes of the individuals were analyzed statistically to find the association between rs4541843 and the breast cancer incidence and its pathological characteristics. The results revealed that due to the dominance of the G allele, the frequency of GG + AG genotypes, as compared with AA, had a significant correlation with the incidence of this disease in controls and cases (P = 0.022; OR = 0.523). Moreover, the genotypes AG and AA could significantly decrease the susceptibility to the breast cancer risk; also in the presence of the A allele (OR, 0.565; P = 0.015), the incidence of the disease could be decreased. Our results indicated that this SNP was associated with the breast cancer risk of the Iranian population. We suppose that rs4541843 may influence the processing of the mature miRNA by affecting the cleavage of Drosha. Therefore, this SNP can be considered as a candidate genetic marker for the susceptibility to breast cancer in the Iranian women.
机译:乳腺癌是世界上最恶性的肿瘤之一。事实上,它是女性癌症死亡的第二大原因。最近的研究已经确定了 miR-182 作为致癌基因因子在这种疾病中的作用。在这项研究中,研究了 miR-182 序列侧翼区域的 rs4541843 与乳腺癌风险易感性的关联。通过使用PCR_RFLP,在 161 名患者和 164 名对照受试者中确定了 rs4541843 基因型。对个体的基因型进行统计学分析,探讨rs4541843与乳腺癌发病率及其病理特征的相关性。结果显示,由于G等位基因的显性,与AA相比,GG+AG基因型的发生率与对照组和病例的发病率有显著相关性(P=0.022;OR = 0.523)。此外,基因型AG和AA可以显著降低乳腺癌的易感性;同样在存在 A 等位基因的情况下 (OR, 0.565;P = 0.015),可以降低该病的发生率。我们的结果表明,该SNP与伊朗人群的乳腺癌风险有关。我们假设 rs4541843 可能通过影响 Drosha 的切割来影响成熟 miRNA 的加工。因此,该SNP可以被认为是伊朗女性乳腺癌易感性的候选遗传标记。

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