• 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

ERCC2基因Lys751Gln多态性与皮肤黑色素瘤易感性关联的综合评估。

Comprehensive assessment of the association of ERCC2 Lys751Gln polymorphism with susceptibility to cutaneous melanoma.

作者信息

Dong Yuhao, Zhuang Le, Ma Weiyuan

机构信息

Shandong University School of Medicine, Jinan, 250012, China.

出版信息

Tumour Biol. 2013 Apr;34(2):1155-60. doi: 10.1007/s13277-013-0657-7. Epub 2013 Feb 3.

DOI:10.1007/s13277-013-0657-7
PMID:23494240
Abstract

Previous studies evaluating the association between excision repair cross-complimentary group 2 (ERCC2) Lys751Gln polymorphism and susceptibility to cutaneous melanoma reported conflicting findings. We searched PubMed and Wangfang Medical databases up to October 16, 2012 to identify eligible studies. A total of 8 case-control studies including 3,492 cases and 5,381 controls were included in the meta-analysis. Statistical analysis was performed with Review Manage version 5.1. Odds ratios (ORs) with 95 % confidence intervals (95 %CIs) were used to assess the strength of the association. There was no obvious between-study heterogeneity among those eight studies under all four comparison models. Overall, there was a significant association between ERCC2 Lys751Gln polymorphism and susceptibility to cutaneous melanoma under three genetic models (for Gln versus Lys: OR = 1.08, 95 % CI = 1.01-1.15, P = 0.02; for GlnGln versus LysLys: OR = 1.16, 95 % CI = 1.01-1.33, P = 0.03; for GlnGln/LysGln versus LysLys: OR = 1.10, 95 % CI = 1.01-1.21, P = 0.04). Sensitivity analysis by omitting one study a time showed the significance of the pooled ORs was stable under all those three genetic models above. Therefore, the meta-analysis suggests that there is a significant association between ERCC2 Lys751Gln polymorphism and susceptibility to cutaneous melanoma.

摘要

先前评估切除修复交叉互补组2(ERCC2)Lys751Gln多态性与皮肤黑色素瘤易感性之间关联的研究报告了相互矛盾的结果。我们检索了截至2012年10月16日的PubMed和万方医学数据库,以确定符合条件的研究。荟萃分析共纳入8项病例对照研究,包括3492例病例和5381例对照。使用Review Manage 5.1版进行统计分析。采用比值比(OR)及其95%置信区间(95%CI)来评估关联强度。在所有四种比较模型下,这八项研究之间均无明显的研究间异质性。总体而言,在三种遗传模型下,ERCC2 Lys751Gln多态性与皮肤黑色素瘤易感性之间存在显著关联(Gln与Lys比较:OR = 1.08,95%CI = 1.01 - 1.15,P = 0.02;GlnGln与LysLys比较:OR = 1.16,95%CI = 1.01 - 1.33,P = 0.03;GlnGln/LysGln与LysLys比较:OR = 1.10,95%CI = 1.01 - 1.21,P = 0.04)。每次剔除一项研究进行的敏感性分析表明,在上述所有三种遗传模型下,合并OR的显著性均稳定。因此,荟萃分析表明ERCC2 Lys751Gln多态性与皮肤黑色素瘤易感性之间存在显著关联。

相似文献

1
Comprehensive assessment of the association of ERCC2 Lys751Gln polymorphism with susceptibility to cutaneous melanoma.ERCC2基因Lys751Gln多态性与皮肤黑色素瘤易感性关联的综合评估。
Tumour Biol. 2013 Apr;34(2):1155-60. doi: 10.1007/s13277-013-0657-7. Epub 2013 Feb 3.
2
Quantitative assessment of the association between XPC Lys939Gln polymorphism and cutaneous melanoma risk.XPC基因Lys939Gln多态性与皮肤黑色素瘤风险关联的定量评估。
Tumour Biol. 2014 Feb;35(2):1427-32. doi: 10.1007/s13277-013-1196-y. Epub 2013 Nov 26.
3
Comprehensive assessment of associations between ERCC2 Lys751Gln/Asp312Asn polymorphisms and risk of non- Hodgkin lymphoma.ERCC2基因Lys751Gln/Asp312Asn多态性与非霍奇金淋巴瘤风险之间关联的综合评估。
Asian Pac J Cancer Prev. 2014;15(21):9347-53. doi: 10.7314/apjcp.2014.15.21.9347.
4
XPD Lys751Gln and Asp312Asn polymorphisms and susceptibility to skin cancer: a meta-analysis of 17 case-control studies.XPD基因Lys751Gln和Asp312Asn多态性与皮肤癌易感性:17项病例对照研究的荟萃分析
Asian Pac J Cancer Prev. 2014;15(16):6619-25. doi: 10.7314/apjcp.2014.15.16.6619.
5
Xeroderma pigmentosum group D polymorphisms and esophageal cancer susceptibility: a meta-analysis based on case-control studies.着色性干皮病D组基因多态性与食管癌易感性:基于病例对照研究的荟萃分析
World J Gastroenterol. 2014 Nov 28;20(44):16765-73. doi: 10.3748/wjg.v20.i44.16765.
6
Predictive value of excision repair cross-complementing group 2 gene Lys751Gln and Asp312Asn polymorphisms in melanoma risk.切除修复交叉互补组2基因Lys751Gln和Asp312Asn多态性对黑色素瘤风险的预测价值。
Melanoma Res. 2018 Aug;28(4):311-318. doi: 10.1097/CMR.0000000000000463.
7
Association between the XPD/ERCC2 Lys751Gln polymorphism and risk of cancer: evidence from 224 case-control studies.XPD/ERCC2基因Lys751Gln多态性与癌症风险的关联:来自224项病例对照研究的证据。
Tumour Biol. 2014 Nov;35(11):11243-59. doi: 10.1007/s13277-014-2379-x. Epub 2014 Aug 13.
8
XPD Lys751Gln polymorphism and esophageal cancer susceptibility: a meta-analysis of case-control studies.XPD Lys751Gln 多态性与食管癌易感性的荟萃分析:病例对照研究。
Mol Biol Rep. 2012 Mar;39(3):2533-40. doi: 10.1007/s11033-011-1005-x. Epub 2011 Jun 11.
9
ERCC2 Lys751Gln polymorphism is associated with lung cancer among Caucasians.核苷酸切除修复交叉互补基因 2 亮氨酸 751 谷氨酰胺多态性与高加索人群肺癌相关。
Eur J Cancer. 2010 Sep;46(13):2479-84. doi: 10.1016/j.ejca.2010.05.008. Epub 2010 Jun 3.
10
A pooled analysis of the ERCC2 Asp312Asn polymorphism and esophageal cancer susceptibility.ERCC2基因Asp312Asn多态性与食管癌易感性的汇总分析。
Tumour Biol. 2014 Apr;35(4):2959-65. doi: 10.1007/s13277-013-1380-0.

引用本文的文献

1
Genomic analysis of a Palestinian family with inherited cancer syndrome: a next-generation sequencing study.一个患有遗传性癌症综合征的巴勒斯坦家庭的基因组分析:一项二代测序研究。
Front Genet. 2023 Oct 31;14:1230241. doi: 10.3389/fgene.2023.1230241. eCollection 2023.
2
Polymorphisms in DNA repair genes in gastrointestinal stromal tumours: susceptibility and correlation with tumour characteristics and clinical outcome.胃肠道间质瘤中DNA修复基因的多态性:易感性及其与肿瘤特征和临床结局的相关性
Tumour Biol. 2016 Oct;37(10):13413-13423. doi: 10.1007/s13277-016-5276-7. Epub 2016 Jul 27.
3
A meta-analysis of XPD/ERCC2 Lys751Gln polymorphism and melanoma susceptibility.

本文引用的文献

1
An ultraviolet-radiation-independent pathway to melanoma carcinogenesis in the red hair/fair skin background.红发/白皙皮肤背景下黑色素瘤发生的紫外线辐射非依赖性途径。
Nature. 2012 Nov 15;491(7424):449-53. doi: 10.1038/nature11624. Epub 2012 Oct 31.
2
The effect of XPD/ERCC2 polymorphisms on gastric cancer risk among different ethnicities: a systematic review and meta-analysis.XPD/ERCC2 多态性对不同种族人群胃癌风险的影响:系统评价和荟萃分析。
PLoS One. 2012;7(9):e43431. doi: 10.1371/journal.pone.0043431. Epub 2012 Sep 13.
3
The role of CCND1 alterations during the progression of cutaneous malignant melanoma.
XPD/ERCC2基因Lys751Gln多态性与黑色素瘤易感性的荟萃分析。
Int J Clin Exp Med. 2015 Aug 15;8(8):13874-8. eCollection 2015.
4
Potentially functional polymorphisms in the ERCC2 gene and risk of esophageal squamous cell carcinoma in Chinese populations.ERCC2基因中潜在的功能性多态性与中国人群食管鳞状细胞癌风险
Sci Rep. 2014 Sep 11;4:6281. doi: 10.1038/srep06281.
5
Association of single nucleotide polymorphisms in ERCC2 gene and their haplotypes with esophageal squamous cell carcinoma.ERCC2基因单核苷酸多态性及其单倍型与食管鳞状细胞癌的关联。
Tumour Biol. 2014 May;35(5):4225-31. doi: 10.1007/s13277-013-1553-x. Epub 2014 Jan 4.
CCND1改变在皮肤恶性黑色素瘤进展过程中的作用。
Tumour Biol. 2012 Dec;33(6):2189-99. doi: 10.1007/s13277-012-0480-6. Epub 2012 Sep 23.
4
The effect of ouabain on mitochondrial DNA damage in HepG2 cell lines.哇巴因对HepG2细胞系线粒体DNA损伤的影响。
Tumour Biol. 2012 Dec;33(6):2107-15. doi: 10.1007/s13277-012-0470-8. Epub 2012 Aug 15.
5
A community-based study of nucleotide excision repair polymorphisms in relation to the risk of non-melanoma skin cancer.基于社区的核苷酸切除修复多态性与非黑色素瘤皮肤癌风险的关系研究。
J Invest Dermatol. 2012 May;132(5):1354-62. doi: 10.1038/jid.2012.4. Epub 2012 Feb 16.
6
Investigation of the effect of MDM2 SNP309 and TP53 Arg72Pro polymorphisms on the age of onset of cutaneous melanoma.探讨 MDM2 SNP309 和 TP53 Arg72Pro 多态性对皮肤黑色素瘤发病年龄的影响。
J Invest Dermatol. 2012 May;132(5):1471-8. doi: 10.1038/jid.2012.15. Epub 2012 Feb 16.
7
Gene expression profiling in MOLT-4 cells during gamma-radiation-induced apoptosis.γ射线辐射诱导MOLT-4细胞凋亡过程中的基因表达谱分析
Tumour Biol. 2012 Jun;33(3):689-700. doi: 10.1007/s13277-012-0329-z. Epub 2012 Feb 10.
8
Reduced expression of DNA repair genes (XRCC1, XPD, and OGG1) in squamous cell carcinoma of head and neck in North India.印度北部头颈部鳞状细胞癌中DNA修复基因(XRCC1、XPD和OGG1)的表达降低。
Tumour Biol. 2012 Feb;33(1):111-9. doi: 10.1007/s13277-011-0253-7. Epub 2011 Nov 15.
9
Effects of ERCC2 Lys751Gln (A35931C) and CCND1 (G870A) polymorphism on outcome of advanced-stage squamous cell carcinoma of the head and neck are treatment dependent.ERCC2 Lys751Gln(A35931C)和 CCND1(G870A)多态性对晚期头颈部鳞状细胞癌结局的影响取决于治疗方法。
Cancer Epidemiol Biomarkers Prev. 2011 Nov;20(11):2429-37. doi: 10.1158/1055-9965.EPI-11-0520. Epub 2011 Sep 2.
10
Evaluation of multiple serum markers in advanced melanoma.晚期黑色素瘤中多种血清标志物的评估
Tumour Biol. 2011 Dec;32(6):1155-61. doi: 10.1007/s13277-011-0218-x. Epub 2011 Aug 20.