• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

白细胞介素6基因多态性rs1800796与癌症风险的关联:一项荟萃分析。

Association of the IL6 polymorphism rs1800796 with cancer risk: a meta-analysis.

作者信息

Du Y, Gao L, Zhang K, Wang J

机构信息

Key Laboratory of Mental Health, Institute of Psychology, Chinese Academy of Sciences, Beijing, China.

Key Laboratory of Mental Health, Institute of Psychology, Chinese Academy of Sciences, Beijing, China

出版信息

Genet Mol Res. 2015 Oct 27;14(4):13236-46. doi: 10.4238/2015.October.26.20.

DOI:10.4238/2015.October.26.20
PMID:26535637
Abstract

The human IL6 [interleukin 6 (interferon, beta 2)] gene encodes IL-6, a cytokine which not only plays regulatory roles in inflammation, but may be also involved in the progression of cancer. Rs1800796 is a single nucleotide polymorphism (SNP) in the promoter region of IL6, and is associated with IL-6 production. A number of studies have been carried out to determine whether this SNP is associated with cancer risk. However, the results are inconsistent due to small sample sizes of individual studies and limited statistical power. Therefore, to evaluate the overall effect on all investigated cancer types, we conducted a meta-analysis by combining all available studies. Nineteen eligible case-control studies including 23,030 subjects (9,985 cases and 13,045 controls) were included for this meta-analysis. Our study demonstrates that rs1800796 is significantly associated with cancer risk in three genetic models (allele G vs allele C, pooled OR = 1.182, P = 0.009; CG + GG vs CC, pooled OR = 1.333, P = 0.006; CG vs CC, pooled OR = 1.323, P = 0.007).Our meta-analysis suggests that polymorphism rs1800796 within the IL6 gene may be a potential risk factor for cancer.

摘要

人类白细胞介素6(IL6)基因编码白细胞介素-6(IL-6),它是一种细胞因子,不仅在炎症中发挥调节作用,还可能参与癌症的进展。Rs1800796是IL6启动子区域的一个单核苷酸多态性(SNP),与IL-6的产生相关。已经开展了许多研究来确定该SNP是否与癌症风险相关。然而,由于个别研究的样本量较小且统计效力有限,结果并不一致。因此,为了评估对所有研究的癌症类型的总体影响,我们通过合并所有可用研究进行了一项荟萃分析。本荟萃分析纳入了19项符合条件的病例对照研究,包括23,030名受试者(9,985例病例和13,045名对照)。我们的研究表明,在三种遗传模型中,rs1800796与癌症风险显著相关(等位基因G与等位基因C,合并比值比=1.182,P=0.009;CG+GG与CC,合并比值比=1.333,P=0.006;CG与CC,合并比值比=1.323,P=0.007)。我们的荟萃分析表明,IL6基因内的多态性rs1800796可能是癌症的一个潜在风险因素。

相似文献

1
Association of the IL6 polymorphism rs1800796 with cancer risk: a meta-analysis.白细胞介素6基因多态性rs1800796与癌症风险的关联:一项荟萃分析。
Genet Mol Res. 2015 Oct 27;14(4):13236-46. doi: 10.4238/2015.October.26.20.
2
Association of the interleukin-6 gene -572G/C polymorphism with cancer risk: a meta-analysis.白细胞介素-6基因-572G/C多态性与癌症风险的关联:一项荟萃分析。
Genet Mol Res. 2015 Dec 14;14(4):16921-8. doi: 10.4238/2015.December.14.20.
3
Association between the interleukin-6-174 G/C polymorphism and risk of ischemic stroke: a meta-analysis.白细胞介素-6 -174 G/C基因多态性与缺血性中风风险的关联:一项荟萃分析。
Genet Mol Res. 2015 Oct 26;14(4):13076-83. doi: 10.4238/2015.October.26.3.
4
Association between IL6 polymorphism and risk of cerebral infarction.白细胞介素6基因多态性与脑梗死风险之间的关联。
Genet Mol Res. 2015 Dec 9;14(4):16438-43. doi: 10.4238/2015.December.9.14.
5
Influence of interleukin-6 gene -174G>C polymorphism on development of atherosclerosis: a meta-analysis of 50 studies involving 33,514 subjects.白细胞介素-6 基因-174G>C 多态性对动脉粥样硬化发展的影响:一项包含 33514 例患者的 50 项研究的荟萃分析。
Gene. 2013 Oct 15;529(1):94-103. doi: 10.1016/j.gene.2013.07.074. Epub 2013 Aug 14.
6
Role of interleukin-6 gene polymorphisms in the development of prostate cancer.白细胞介素-6基因多态性在前列腺癌发生发展中的作用。
Genet Mol Res. 2015 Oct 27;14(4):13370-4. doi: 10.4238/2015.October.26.34.
7
Interleukin-6-174G>C gene promoter polymorphism and prognosis in patients with cancer.白细胞介素-6基因启动子-174G>C多态性与癌症患者的预后
Oncotarget. 2017 Jul 4;8(27):44490-44497. doi: 10.18632/oncotarget.17771.
8
Association between the -607 C > A polymorphism in interleukin-18 gene promoter with gastrointestinal cancer risk: a meta-analysis.白细胞介素-18基因启动子-607C>A多态性与胃肠道癌风险的关联:一项荟萃分析。
Genet Mol Res. 2015 Dec 14;14(4):16880-7. doi: 10.4238/2015.December.14.15.
9
Interleukin-6 -572G/C polymorphism and prostate cancer susceptibility.白细胞介素-6 -572G/C基因多态性与前列腺癌易感性
Genet Mol Res. 2016 Sep 16;15(3):gmr7563. doi: 10.4238/gmr.15037563.
10
IL-1β+3953C/T, -511T/C and IL-6 -174C/G polymorphisms in association with tuberculosis susceptibility: A meta-analysis.白细胞介素-1β +3953C/T、-511T/C多态性及白细胞介素-6 -174C/G多态性与结核病易感性的关联:一项荟萃分析
Gene. 2015 Nov 15;573(1):75-83. doi: 10.1016/j.gene.2015.07.025. Epub 2015 Jul 11.

引用本文的文献

1
and genetic variations and gastric cancer risk in the Chinese population.以及中国人群中的基因变异与胃癌风险。
Am J Transl Res. 2019 Jun 15;11(6):3698-3706. eCollection 2019.
2
Association study of genetic variations of inflammatory biomarkers with susceptibility and severity of obstructive sleep apnea.炎症生物标志物遗传变异与阻塞性睡眠呼吸暂停易感性和严重程度的关联研究。
Mol Genet Genomic Med. 2019 Aug;7(8):e801. doi: 10.1002/mgg3.801. Epub 2019 Jun 18.
3
The Role of Polymorphisms in Genes of PI3K/Akt Signaling Pathway on Prostate.
PI3K/Akt信号通路基因多态性在前列腺中的作用
J Cancer. 2019 Jan 29;10(4):1023-1031. doi: 10.7150/jca.26472. eCollection 2019.
4
Differentially expressed microRNAs in lung adenocarcinoma invert effects of copy number aberrations of prognostic genes.肺腺癌中差异表达的微小RNA反转预后基因拷贝数变异的作用。
Oncotarget. 2018 Jan 8;9(10):9137-9155. doi: 10.18632/oncotarget.24070. eCollection 2018 Feb 6.
5
Determination of (rs16944) and (rs1800796) genetic polymorphisms in IgA nephropathy in a northwest Chinese Han population.中国西北汉族人群中IgA肾病患者(rs16944)和(rs1800796)基因多态性的测定
Oncotarget. 2017 May 4;8(42):71750-71758. doi: 10.18632/oncotarget.17603. eCollection 2017 Sep 22.
6
Possible role of IL-6 and TIE2 gene polymorphisms in predicting the initial high transport status in patients with peritoneal dialysis: an observational study.白细胞介素-6和TIE2基因多态性在预测腹膜透析患者初始高转运状态中的可能作用:一项观察性研究。
BMJ Open. 2016 Oct 26;6(10):e012967. doi: 10.1136/bmjopen-2016-012967.