Suppr超能文献

[基因名称]启动子区域新型基因变异与结直肠癌风险之间的关联。 (注:原文中“of”后面缺少具体基因名称,这里用[基因名称]表示)

Associations between novel genetic variants in the promoter region of and risk of colorectal cancer.

作者信息

Li Yingjun, Bao Chengzhen, Gu Simeng, Ye Ding, Jing Fangyuan, Fan Chunhong, Jin Mingjuan, Chen Kun

机构信息

Department of Epidemiology and Health Statistics, Zhejiang University School of Public Health, Hangzhou, China.

Department of Public Health, Hangzhou Medical College, Hangzhou, China.

出版信息

Oncotarget. 2017 Oct 4;8(54):92604-92614. doi: 10.18632/oncotarget.21507. eCollection 2017 Nov 3.

Abstract

The metastasis-associated lung adenocarcinoma transcript 1 (), a well-known long non-coding RNA, is involved in pathogenesis and progress of multiple tumors. However, no study has been performed to investigate the relationship between the genetic variants in promoter region of and colorectal cancer risk. In this study, we conducted a two-stage case-control study to evaluate whether genetic variants were associated with colorectal cancer risk. We identified that a single nucleotide polymorphism (SNP) rs1194338 was significantly associated with the decreased colorectal cancer risk with an odds ratio (OR) of 0.70 [95% confidence interval (CI) = 0.49-0.99] in the combined stage. The subsequently stratified analyses showed that the protective effect of rs1194338 was more pronounced in several subgroups. Furthermore, gene expression profiling analysis revealed overexpression of mRNA in colorectal cancer tissue compared with normal controls. Confirmation studies with large sample size and further mechanistic investigations into the function of and its genetic variants are warranted to advance our understanding of their roles in colorectal carcinogenesis, and to aid in the development of novel and targeted therapeutic strategies.

摘要

转移相关的肺腺癌转录本1()是一种著名的长链非编码RNA,参与多种肿瘤的发病机制和进展。然而,尚未有研究探讨其启动子区域的基因变异与结直肠癌风险之间的关系。在本研究中,我们进行了一项两阶段病例对照研究,以评估基因变异是否与结直肠癌风险相关。我们发现,在合并阶段,单核苷酸多态性(SNP)rs1194338与结直肠癌风险降低显著相关,比值比(OR)为0.70 [95%置信区间(CI)= 0.49 - 0.99]。随后的分层分析表明,rs1194338的保护作用在几个亚组中更为明显。此外,基因表达谱分析显示,与正常对照相比,结直肠癌组织中mRNA表达上调。有必要进行大样本量的验证研究,并对及其基因变异的功能进行进一步的机制研究,以加深我们对它们在结直肠癌发生中的作用的理解,并有助于开发新的靶向治疗策略。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验