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MicroRNAs (miRNAs) are non-coding RNAs that function as regulators of tumor suppressors and oncogenes. A G>C polymorphism (rs2910164) in the miR‑146a precursor sequence leads to a functional change associated with a risk for various types of malignancy. The role of this single nucleotide polymorphism in the pathogenesis of renal cell carcinoma (RCC) has not yet been examined. The present study evaluated the association between rs2910164 genotypes and the risk and prognosis of RCC in a population comprised of 421 RCC cases and 432 controls. Unconditional logistic regression was used to estimate odds ratios (OR) and 95% confidence intervals (CI) for rs2910164 genotypes according to case status. Cox proportional hazards regression modeling was used to estimate hazards ratios and 95% CIs according to the genotypes among the RCC patients. It was found that the rs2910164 GG and GC genotypes were associated with an increased risk of RCC only in senior subjects (>57‑years old; adjusted OR=1.59, 95% CI=1.04‑2.43). Furthermore, the GC and GG genotypes were associated with a poorer survival rate among patients with RCC compared with the CC genotype (P=0.002). In conclusion, the observed association between the GG and GC genotype and poorer survival rate of RCC was at least partially mediated by the decreased expression of miR-146a.
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http://dx.doi.org/10.3892/mmr.2015.4260 | DOI Listing |
Per Med
August 2025
Molecular Biology Lab, Department of Zoology, University of Jammu, Jammu and Kashmir, India.
Background: Prostate cancer (CaP) is the most commonly diagnosed malignant tumor and the leading cause of cancer-related deaths among men. Due to their potential functional significance, microRNA genes are considered promising candidates for identifying cancer-related genetic biomarkers. This study investigates the association between microRNA-196a2 (rs11614913), microRNA-146a (rs2910164), and microRNA-149 (rs2292832) and the risk of prostate cancer among males in the Jammu region of Jammu and Kashmir (J&K).
View Article and Find Full Text PDFInt J Fertil Steril
July 2025
Department of Biology, Ars.C., Islamic Azad University, Arsanjan, Iran. Email:
Background: Idiopathic Male Infertility is a widespread problem affecting approximately 10 to 15 percent of men of reproductive age. Several genes have been studied related to idiopathic male infertility. Thereafter, among the family of non-coding RNAs, microRNAs are shown to play a very important role in the regulation of a subset of genes.
View Article and Find Full Text PDFInt J Gynaecol Obstet
June 2025
Postgraduate Program in Science Applied to Women's Health, Federal University of Rio Grande Do Norte, Natal, Rio Grande do Norte, Brazil.
Background: Polycystic ovary syndrome (PCOS) is a prevalent endocrine disorder in women of reproductive age, associated with genetic and environmental factors, including microRNA (miRNA) gene polymorphisms.
Objective: To evaluate the association between miRNA gene polymorphisms and PCOS.
Search Strategy: PubMed, Embase, Web of Science, and Scopus databases were searched to September 2024, using MeSH terms including "MicroRNAs", "Polymorphism, Single Nucleotide," and "Polycystic Ovary Syndrome".
Mol Syndromol
May 2025
Department of Psychiatry and Psychology, JingNing People's Hospital, Pingliang, China.
Introduction: The incidence of depression in adolescents is increasing and is associated with severe cognitive impairment. This paper aimed to investigate the relationship between polymorphisms in microRNA-146a-5p (miR-146a-5p) and cognitive impairment in adolescent depression patients.
Methods: Quantitative real-time polymerase chain reaction was used to quantify miR-146a-5p in serum.
Biomark Med
June 2025
Department of Human Genetics, Sri Ramachandra Institute of Higher Education and Research, Chennai, India.
Introduction: MicroRNA (miRNA) single nucleotide polymorphisms (miRNA-SNPs) have been associated with pediatric acute lymphoblastic leukemia (ALL). However, since the results of these individual studies have been inconsistent, we performed a meta-analysis to help establish a statistical significance for the association between miRNA-SNPs and pediatric ALL risk. We also analyzed whether they confer susceptibility across country-specific studies by using different genetic models.
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