The Significant Contribution of LINC00673 Rs11655237 C > T Polymorphism to Cancer Susceptibility in Chinese Population: A Meta-analysis of The Current Literature

Xuejiao Guan, Peng Du, Yong Li, Qingfeng Xiao, J. Tan, Xingjian Zhang
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引用次数: 1

Abstract

Abstract: Objective Considerable studies exploring the relation of rs11655237 C > T polymorphism in the LINC00673 gene with cancer susceptibility have obtained debatable results. This meta-analysis aims to accurately assess this association. Methods Relevant studies with an updated date of April 20, 2021, were extensively searched from Embase, PubMed, Web of Science, Google Scholar, Medline, CNKI, and Chinese Wanfang databases. The strength of association was estimated by odds ratios (ORs) and 95% confidence intervals (CIs). Results A total of 8 articles involving 7,893 cases and 12,446 controls were ultimately selected in this analysis. Summary results revealed a significantly enhanced risk of cancer was related to LINC00673 rs11655237 C > T polymorphism for the allele model (OR = 1.22, 95% CI = 1.09-1.36), homozygote model (OR = 1.47, 95% CI = 1.30-1.67), heterozygote model (OR = 1.21, 95% CI = 1.14-1.29), dominant model (OR = 1.25, 95% CI = 1.18-1.32), and recessive model (OR = 1.26, 95% CI = 1.12-1.43). Moreover, subgroup analysis by cancer type showed LINC00673 rs11655237 C > T polymorphism contributed to the increased risk of neuroblastoma in the heterozygote, homozygote, dominant and recessive models. Conclusion The present meta-analysis indicates that LINC00673 rs11655237 C > T polymorphism is related to increased cancer susceptibility in the Chinese population. It may be a potential predictive biomarker of cancer risk.
LINC00673 Rs11655237 C > T多态性对中国人群癌症易感性的显著贡献:对当前文献的荟萃分析
摘要:目的对LINC00673基因rs11655237 C > T多态性与癌症易感性的关系进行了大量的研究,得到了有争议的结果。本荟萃分析旨在准确评估这种关联。方法从Embase、PubMed、Web of Science、b谷歌Scholar、Medline、CNKI、中国万方等数据库广泛检索更新日期为2021年4月20日的相关研究。关联强度通过比值比(ORs)和95%置信区间(ci)估计。结果共纳入8篇文献,7893例病例,12446例对照。综上所示,癌症风险显著增加与等位基因模型(OR = 1.22, 95% CI = 1.09-1.36)、纯合子模型(OR = 1.47, 95% CI = 1.30-1.67)、杂合子模型(OR = 1.21, 95% CI = 1.14-1.29)、显性模型(OR = 1.25, 95% CI = 1.18-1.32)和隐性模型(OR = 1.26, 95% CI = 1.12-1.43)的LINC00673 rs11655237 C > T多态性相关。此外,根据癌症类型进行亚组分析显示,在杂合子、纯合子、显性和隐性模型中,LINC00673 rs11655237 C > T多态性导致神经母细胞瘤的风险增加。结论本荟萃分析表明,LINC00673 rs11655237 C > T多态性与中国人群癌症易感性增加有关。它可能是癌症风险的潜在预测性生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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