Mobaraki Marzieh, Aghdaei Hamid Asadzadeh, Angaji Seyed Abdolhamid, Nazemalhosseini-Mojarad Ehsan, Arbabian Sedigheh
Department of Biology, Faculty of Biological Sciences, Islamic Azad University, North Tehran Branch, Tehran, Iran.
Basic and Molecular Epidemiology of Gastrointestinal Disorders Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Iran J Public Health. 2024 Dec;53(12):2812-2822.
We aimed to elucidate the potential correlation between single-nucleotide polymorphisms (SNPs) in miRNA machinery genes and colorectal cancer (CRC) risk in an Iranian cohort.
We conducted a robust case-control study involving 507 participants, which included 213 patients diagnosed with CRC and 294 healthy controls at Research Institute for Gastroenterology and Liver Diseases in Tehran Province, Iran in 2018. The study focused on genotyping four specific SNPs, (rs14035), (rs197412), (rs2740348), and (rs3742330), using advanced ARMS-PCR and Tetra-primer ARMS-PCR techniques.
Notably, our investigation revealed the significant inverse association between the C/C genotype of rs197412 in the gene and CRC risk (OR=0.54, 95% CI=0.33-0.87; =0.0087). In stark contrast, the T/T genotype of rs14035 in the gene was strongly associated with a heightened risk of developing CRC (OR=4.44, 95% CI=2.60-7.57, <0.0001). Furthermore, we found that the G/G genotype of rs2740348 in posed an increased risk for CRC (OR=2.9, 95% CI=1.44-5.85, =0.0041) and it has a major effect on CRC risk in our population. The alleles and genotypes of rs3742330 in , however, did not exhibit a significant correlation with CRC.
Our study provides compelling evidence that SNPs within miRNA processing genes significantly contribute to susceptibility to CRC among the Iranian population. Our research not only contributes to the growing body of miRNA-related genetic studies but also opens avenues for population-specific risk assessment and personalized medicine approaches in cancer therapy.
我们旨在阐明伊朗人群中微小RNA(miRNA)机制基因中的单核苷酸多态性(SNP)与结直肠癌(CRC)风险之间的潜在关联。
我们进行了一项严格的病例对照研究,涉及507名参与者,其中包括2018年在伊朗德黑兰省胃肠病和肝病研究所诊断为CRC的213名患者和294名健康对照。该研究使用先进的扩增阻滞突变系统聚合酶链反应(ARMS-PCR)和四引物ARMS-PCR技术,对四个特定的SNP,即(rs14035)、(rs197412)、(rs2740348)和(rs3742330)进行基因分型。
值得注意的是,我们的研究揭示了基因中rs197412的C/C基因型与CRC风险之间存在显著的负相关(比值比[OR]=0.54,95%置信区间[CI]=0.33 - 0.87;P=0.0087)。与之形成鲜明对比的是,基因中rs14035的T/T基因型与患CRC的风险显著升高密切相关(OR=4.44,95% CI=2.60 - 7.57,P<0.0001)。此外,我们发现基因中rs2740348的G/G基因型增加了患CRC的风险(OR=2.9,95% CI=1.44 - 5.85,P=0.0041),并且它对我们人群中的CRC风险有重大影响。然而,基因中rs3742330的等位基因和基因型与CRC没有显著相关性。
我们的研究提供了有力证据,表明miRNA加工基因中的SNP对伊朗人群中CRC的易感性有显著影响。我们的研究不仅为不断增加的与miRNA相关的基因研究做出了贡献,也为癌症治疗中针对特定人群的风险评估和个性化医疗方法开辟了道路。