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VPS9D1-AS1 基因 rs7206570 多态性与结直肠癌的临床分期相关,并与 hsa-miR-361-3p 结合。

VPS9D1-AS1 gene rs7206570 polymorphism associated with the clinical stage of colorectal cancer and binding with hsa-miR-361-3p.

机构信息

School of Pharmacy, Yancheng Teachers' University, 2 Hope Avenue South Road, Yancheng, 224007, Jiangsu, China.

Department of General Surgery, Xuhui District Central Hospital, Shanghai, 200030, China.

出版信息

Hum Cell. 2022 Mar;35(2):522-527. doi: 10.1007/s13577-021-00658-1. Epub 2022 Jan 13.

Abstract

VPS9D1-AS1 is a long non-coding RNA that can operate as a competitive endogenous RNA and plays an essential role in the occurrence and development of malignancies, including colorectal cancer (CRC). In this study, we investigated whether a putative functional polymorphism (rs7206570) in the VPS9D1-AS1 gene is linked to the risk and clinical stage of CRC. Sanger sequencing method was used to detect the rs7206570 polymorphism in 500 CRC patients and 500 healthy individuals. Quantitative real-time PCR technology was used to detect the expression of VPS9D1-AS1 and hsa-miR-361-3p in colorectal tissues with different rs7206570 genotypes. The dual-luciferase reporter assay was used to examine whether the rs7206570 polymorphism affects hsa-miR-361-3p binding. The rs7206570 polymorphism was not associated with CRC risk, but was associated with the clinical stage of CRC. CRC patients with rs7206570 A allele were less likely to have high-stage CRC. Furthermore, there was a significant negative correlation between the expression of VPS9D1-AS1 and hsa-miR-361-3p in CRC tissues with rs7206570 GG genotype. Dual-luciferase reporter assay showed that the rs7206570 A allele presumably hinders the binding of VPS9D1-AS1 to hsa-miR-361-3p. In conclusion, VPS9D1-AS1 gene rs7206570 polymorphism affecting hsa-miR-361-3p binding was associated with the clinical stage of CRC, which might be able to assist in the preoperative staging of CRC.

摘要

VPS9D1-AS1 是一种长链非编码 RNA,可作为竞争性内源性 RNA 发挥作用,在包括结直肠癌(CRC)在内的恶性肿瘤的发生和发展中起着至关重要的作用。在这项研究中,我们研究了 VPS9D1-AS1 基因中的一个假定功能多态性(rs7206570)是否与 CRC 的风险和临床分期有关。我们使用 Sanger 测序法检测了 500 例 CRC 患者和 500 例健康个体中 rs7206570 多态性。使用定量实时 PCR 技术检测不同 rs7206570 基因型的结直肠组织中 VPS9D1-AS1 和 hsa-miR-361-3p 的表达。双荧光素酶报告基因实验用于检测 rs7206570 多态性是否影响 hsa-miR-361-3p 的结合。rs7206570 多态性与 CRC 风险无关,但与 CRC 的临床分期有关。携带 rs7206570A 等位基因的 CRC 患者更不可能患有晚期 CRC。此外,在 rs7206570GG 基因型的 CRC 组织中,VPS9D1-AS1 和 hsa-miR-361-3p 的表达呈显著负相关。双荧光素酶报告基因实验显示,rs7206570A 等位基因可能会阻碍 VPS9D1-AS1 与 hsa-miR-361-3p 的结合。总之,VPS9D1-AS1 基因 rs7206570 多态性影响 hsa-miR-361-3p 的结合与 CRC 的临床分期有关,这可能有助于 CRC 的术前分期。

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