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Investigative Role of Pre-MicroRNAs in Bladder Cancer Patients: A Case-Control Study in North India

机译:前MicroRNAs在膀胱癌患者中的调查作用:在印度北部的病例对照研究。

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摘要

MicroRNAs (miRNA) are a class of small noncoding RNA molecules that have been implicated in a wide variety of cellular functions through post-transcriptional regulations on target genes. Common genetic variants (single-nucleotide polymorphisms, SNPs) in pre-miRNA genes may alter their expression and/or maturation effecting thousands of target mRNAs, resulting in varied functional consequences. Three common SNPs (hsa-mir-146a G>C rs2910164, hsa-mir-196a2 C>T rs11614913, and hsa-mir-499 T>C rs3746444) in pre-miRNAs were investigated to evaluate their association with urinary bladder cancer risk. The hospital-based case-control study comprised of 212 histologically confirmed patients with urinary bladder cancer and 250 healthy controls who were unrelated, of similar ethnicity, and age and gender matched. Genotyping was done using polymerase chain reaction-restriction fragment length polymorphism methodology. Our results showed that the heterozygous genotype of rs11614913 was higher in cases than controls but the results were marginally significant (p = 0.055; odds ratio, 1.44). Smoking had no impact in modulating the effect of any of the three miRNA SNPs studied. No association was observed with either the tumor stage or grade in patients with bladder cancer. Even though there was no association between the individuals carrying the variant genotypes of the three miRNA studied and bladder cancer risk, marginal significance of heterozygousity in rs11614913 suggested further characterization of miRNA SNPs in a large cohort of varied ethnicity. This could further provide new prospects for understanding the underlying mechanisms between miRNAs and disease etiology.
机译:MicroRNA(miRNA)是一类小的非编码RNA分子,通过对靶标基因的转录后调控,它们参与了多种细胞功能。 pre-miRNA基因中常见的遗传变异(单核苷酸多态性,SNP)可能会改变它们的表达和/或成熟,从而影响成千上万的靶mRNA,从而导致各种各样的功能性后果。研究了pre-miRNA中的三种常见SNP(hsa-mir-146a G> C rs2910164,hsa-mir-196a2 C> T rs11614913和hsa-mir-499 T> C rs3746444),以评估它们与膀胱癌风险的相关性。这项基于医院的病例对照研究包括212例​​经组织学证实的膀胱癌患者和250例不相关,种族相似,年龄和性别相匹配的健康对照。使用聚合酶链反应-限制性片段长度多态性方法进行基因分型。我们的结果表明,rs11614913的杂合基因型在病例中高于对照组,但结果略有显着性(p = 0.055;优势比为1.44)。吸烟对调节所研究的三种miRNA SNP中任何一种的作用均无影响。膀胱癌患者与肿瘤分期或分级均无关联。即使携带所研究的三种miRNA的变异基因型的个体与膀胱癌风险之间没有关联,rs11614913中杂合性的边际意义也提示了在许多不同种族的人群中miRNA SNP的进一步表征。这可能进一步为了解miRNA与疾病病因之间的潜在机制提供新的前景。

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