SMAD7 基因多态性及其对结直肠癌患者的影响。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2023-11-01 Epub Date: 2024-01-18 DOI:10.1080/15384101.2023.2296210
Yongsheng Wu, Jue Xu, Biaobin Tan, Ting Yi, Su Liu, Guang Yang, Kai Li, Xinhan Zhao
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引用次数: 0

摘要

结直肠癌(CRC)是一种常见的恶性肿瘤,其发病机制至今仍未完全明了。研究表明,SMAD7 基因多态性可影响 CRC 易感性,但结果并不一致,需要进一步证实。我们的研究旨在评估SMAD7变异对中国汉族人群CRC风险的影响。我们使用 MassARRAY iPLEX 平台对 696 名 CRC 患者和 696 名健康参与者进行了 SMAD7 中 5 个单核苷酸多态性(SNPs)的基因分型。利用多重遗传模型下的逻辑回归分析评估了 SNP 与 CRC 的相关性。假阳性报告概率(FPRP)分析用于验证阳性结果。我们的研究表明,rs11874392 与 CRC 风险的相关性增加(几率比,1.31;95% 置信区间,1.04-1.67;p = 0.024)。分层分析表明,rs11874392 可能会增加女性(OR = 1.70,p = 0.028)、吸烟(OR = 1.87,p = 0.026)和饮酒(OR = 1.38,p = 0.027)人群的 CRC 风险。研究发现,rs11874392 与直肠癌风险升高有关(OR = 1.73,p = 0.003),但与结肠癌无关。FPRP 分析表明,所有这些关联都具有统计学意义(FPRP SMAD7 rs11874392 与 CRC 易感性增加有关。
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SMAD7 gene polymorphisms and their influence on patients with colorectal cancer.

Colorectal cancer (CRC) is a prevalent malignant tumor, and its pathogenesis is still not fully understood. Studies have shown that SMAD7 gene polymorphisms can affect CRC susceptibility, but the results have been inconsistent and require additional confirmation. Our study aimed to evaluate the effect of SMAD7 variants on the risk of CRC in the Chinese Han population. A total of five single nucleotide polymorphisms (SNPs) in SMAD7 were genotyped among 696 CRC patients and 696 healthy participants using the MassARRAY iPLEX platform. SNPs were evaluated for their associations with CRC using logistic regression analysis under multiple genetic models. The false-positive report probability (FPRP) analysis was used to validate the positive findings. Our study indicated that rs11874392 showed an increased association with CRC risk (odds ratio, 1.31; 95% confidence interval, 1.04-1.67; p = 0.024). Stratified analysis showed that rs11874392 might increase the risk of CRC in females (OR = 1.70, p = 0.028), individuals with smoking (OR = 1.87, p = 0.026), and drinking (OR = 1.38, p = 0.027). The rs11874392 was found to be related to an elevated risk of rectal cancer (OR = 1.73, p = 0.003), but not with colon cancer. FPRP analysis demonstrated that all of these associations were statistically significant (FPRP <0.2). Additionally, rs11874392 was the strongest predictive model for CRC. This study provides evidence that the SMAD7 rs11874392 is related to an increased susceptibility to CRC.

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