• 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

PARP-1 Val762Ala 多态性与韩国男性非霍奇金淋巴瘤风险降低相关。

PARP-1 Val762Ala polymorphism is associated with reduced risk of non-Hodgkin lymphoma in Korean males.

机构信息

Genome Research Center for Hematopoietic Diseases, Chonnam National University Hwasun Hospital, 160, Ilsim-ni, Hwasun-eup, Hwasun-gun, Chonnam, 519-809, Republic of Korea.

出版信息

BMC Med Genet. 2010 Mar 3;11:38. doi: 10.1186/1471-2350-11-38.

DOI:10.1186/1471-2350-11-38
PMID:20196871
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2843603/
Abstract

BACKGROUND

Poly(ADP-ribose) polymerase-1 (PARP-1) is a nuclear enzyme that plays a role in DNA repair, differentiation, proliferation, and cell death. The polymorphisms of PARP-1 have been associated with the risk of various carcinomas, including breast, lung, and prostate. We investigated whether PARP-1 polymorphisms are associated with the risk of non-Hodgkin lymphoma (NHL).

METHODS

Subjects from a Korean population consisting of 573 NHL patients and 721 controls were genotyped for 5 PARP-1 polymorphisms (Asp81Asp, Ala284Ala, Lys352Lys, IVS13+118A>G, and Val762Ala) using High Resolution Melting polymerase chain reaction (PCR) and an automatic sequencer.

RESULTS

None of the 5 polymorphisms were associated with overall risk for NHL. However, the Val762Ala polymorphism was associated with reduced risk for NHL in males [odds ratio (OR), 0.62; 95% confidence interval (CI), 0.41-0.93 for CC genotype and OR, 0.84; 95% CI, 0.60-1.16 for TC genotype] with a trend toward a gene dose effect (p for trend, 0.02). The Asp81Asp (p for trend, 0.04) and Lys352Lys (p for trend, 0.03) polymorphisms revealed the same trend. In an association study of PARP-1 haplotypes, the haplotype-ACAAC was associated with decreased risk of NHL in males (OR, 0.75; 95% CI, 0.59-0.94).

CONCLUSION

The present data suggest that Val762Ala, Asp81Asp, and Lys352Lys polymorphisms and the haplotype-ACAAC in PARP-1 are associated with reduced risk of NHL in Korean males.

摘要

背景

多聚(ADP-核糖)聚合酶-1(PARP-1)是一种核酶,在 DNA 修复、分化、增殖和细胞死亡中发挥作用。PARP-1 的多态性与各种癌的风险相关,包括乳腺癌、肺癌和前列腺癌。我们研究了 PARP-1 多态性是否与非霍奇金淋巴瘤(NHL)的风险相关。

方法

来自韩国人群的 573 例 NHL 患者和 721 例对照者的研究对象使用高分辨率熔解聚合酶链反应(PCR)和自动测序仪对 5 个 PARP-1 多态性(Asp81Asp、Ala284Ala、Lys352Lys、IVS13+118A>G 和 Val762Ala)进行了基因分型。

结果

这 5 个多态性均与 NHL 的总体风险无关。然而,Val762Ala 多态性与男性 NHL 风险降低相关[优势比(OR),0.62;95%置信区间(CI),0.41-0.93 对于 CC 基因型和 OR,0.84;95%CI,0.60-1.16 对于 TC 基因型],且存在基因剂量效应的趋势(趋势检验的 P 值为 0.02)。Asp81Asp(P 趋势,0.04)和 Lys352Lys(P 趋势,0.03)多态性也呈现出相同的趋势。在 PARP-1 单倍型的关联研究中,ACAAC 单倍型与男性 NHL 风险降低相关(OR,0.75;95%CI,0.59-0.94)。

结论

本研究数据表明,PARP-1 中的 Val762Ala、Asp81Asp 和 Lys352Lys 多态性以及 ACAAC 单倍型与韩国男性 NHL 风险降低相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eefc/2843603/8d0e636eb3f0/1471-2350-11-38-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eefc/2843603/8d0e636eb3f0/1471-2350-11-38-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eefc/2843603/8d0e636eb3f0/1471-2350-11-38-1.jpg

相似文献

1
PARP-1 Val762Ala polymorphism is associated with reduced risk of non-Hodgkin lymphoma in Korean males.PARP-1 Val762Ala 多态性与韩国男性非霍奇金淋巴瘤风险降低相关。
BMC Med Genet. 2010 Mar 3;11:38. doi: 10.1186/1471-2350-11-38.
2
Lack of association between poly(ADP-ribose) polymerase (PARP) polymorphisms and rheumatoid arthritis in a Korean population.聚(ADP-核糖)聚合酶(PARP)多态性与韩国人群类风湿关节炎之间缺乏关联。
Rheumatol Int. 2012 Jan;32(1):91-6. doi: 10.1007/s00296-010-1589-9. Epub 2010 Jul 28.
3
Involvement of PARP-1 Val762Ala polymorphism in the onset of cervical cancer in caucasian women.PARP-1 Val762Ala 多态性与白人女性宫颈癌的发病有关。
Mol Diagn Ther. 2013 Aug;17(4):239-45. doi: 10.1007/s40291-013-0036-5.
4
PARP-1 Val762Ala polymorphism is associated with risk of cervical carcinoma.PARP-1 Val762Ala 多态性与宫颈癌风险相关。
PLoS One. 2012;7(5):e37446. doi: 10.1371/journal.pone.0037446. Epub 2012 May 18.
5
Correlation between PARP-1 Val762Ala polymorphism and the risk of lung cancer in a Chinese population.PARP-1基因Val762Ala多态性与中国人群肺癌风险的相关性
Tumour Biol. 2015 Jan;36(1):177-81. doi: 10.1007/s13277-014-2373-3. Epub 2014 Sep 2.
6
The Ala allele at Val762Ala polymorphism in poly(ADP-ribose) polymerase-1 (PARP-1) gene is associated with a decreased risk of asthma in a Turkish population.聚(ADP - 核糖)聚合酶 -1(PARP - 1)基因中Val762Ala多态性的丙氨酸(Ala)等位基因与土耳其人群哮喘风险降低相关。
J Asthma. 2009 May;46(4):371-4. doi: 10.1080/02770900902777791.
7
Modulation of brain tumor risk by genetic SNPs in PARP1gene: Hospital based case control study.PARP1 基因中遗传 SNP 对脑肿瘤风险的调节:基于医院的病例对照研究。
PLoS One. 2019 Oct 14;14(10):e0223882. doi: 10.1371/journal.pone.0223882. eCollection 2019.
8
PARP-1 Val762Ala polymorphism, CagA+ H. pylori infection and risk for gastric cancer in Han Chinese population.PARP-1基因第762位密码子缬氨酸到丙氨酸多态性、CagA阳性幽门螺杆菌感染与中国汉族人群胃癌风险
Mol Biol Rep. 2009 Jul;36(6):1461-7. doi: 10.1007/s11033-008-9336-y. Epub 2008 Aug 21.
9
The Val762Ala polymorphism in the poly(ADP-ribose) polymerase-1 gene is not associated with susceptibility in Turkish rheumatoid arthritis patients.聚(ADP - 核糖)聚合酶 -1基因中的Val762Ala多态性与土耳其类风湿性关节炎患者的易感性无关。
Rheumatol Int. 2009 May;29(7):797-800. doi: 10.1007/s00296-008-0772-8. Epub 2008 Nov 22.
10
H2AFX polymorphisms are associated with decreased risk of diffuse large B cell lymphoma in Koreans.H2AFX 多态性与韩国人弥漫性大 B 细胞淋巴瘤风险降低相关。
DNA Cell Biol. 2011 Dec;30(12):1039-44. doi: 10.1089/dna.2010.1130. Epub 2011 Jun 1.

引用本文的文献

1
rs1136410 Val762Ala contributes to an increased risk of overall cancer in the East Asian population: a meta-analysis.rs1136410 Val762Ala 增加东亚人群总体癌症风险:一项荟萃分析。
J Int Med Res. 2021 Mar;49(3):300060521992956. doi: 10.1177/0300060521992956.
2
Interaction among susceptibility genotypes of PARP1 SNPs in thyroid carcinoma.甲状腺癌中 PARP1 SNPs 易感性基因型的相互作用。
PLoS One. 2018 Sep 5;13(9):e0199007. doi: 10.1371/journal.pone.0199007. eCollection 2018.
3
PARP-1 Val762Ala polymorphism and risk of cancer: a meta-analysis based on 39 case-control studies.

本文引用的文献

1
Association and interactions between DNA repair gene polymorphisms and adult glioma.DNA修复基因多态性与成人胶质瘤之间的关联及相互作用。
Cancer Epidemiol Biomarkers Prev. 2009 Jan;18(1):204-14. doi: 10.1158/1055-9965.EPI-08-0632.
2
PARP-1 Val762Ala polymorphism, CagA+ H. pylori infection and risk for gastric cancer in Han Chinese population.PARP-1基因第762位密码子缬氨酸到丙氨酸多态性、CagA阳性幽门螺杆菌感染与中国汉族人群胃癌风险
Mol Biol Rep. 2009 Jul;36(6):1461-7. doi: 10.1007/s11033-008-9336-y. Epub 2008 Aug 21.
3
Polygenic model of DNA repair genetic polymorphisms in human breast cancer risk.
聚(ADP-核糖)聚合酶-1(PARP-1)第762位缬氨酸到丙氨酸多态性与癌症风险:基于39项病例对照研究的荟萃分析
PLoS One. 2014 May 22;9(5):e98022. doi: 10.1371/journal.pone.0098022. eCollection 2014.
4
Association between the PARP1 Val762Ala polymorphism and cancer risk: evidence from 43 studies.PARP1基因Val762Ala多态性与癌症风险的关联:来自43项研究的证据。
PLoS One. 2014 Jan 28;9(1):e87057. doi: 10.1371/journal.pone.0087057. eCollection 2014.
5
Therapeutic applications of PARP inhibitors: anticancer therapy and beyond.PARP 抑制剂的治疗应用:抗癌治疗及其他。
Mol Aspects Med. 2013 Dec;34(6):1217-56. doi: 10.1016/j.mam.2013.01.006. Epub 2013 Jan 29.
6
The roles of beta-adrenergic receptors in tumorigenesis and the possible use of beta-adrenergic blockers for cancer treatment: possible genetic and cell-signaling mechanisms.β-肾上腺素能受体在肿瘤发生中的作用及β-肾上腺素能阻滞剂在癌症治疗中的可能应用:可能的遗传和细胞信号转导机制。
Cancer Manag Res. 2012;4:431-45. doi: 10.2147/CMAR.S39153. Epub 2012 Dec 18.
7
Lack of an association between two BER gene polymorphisms and breast cancer risk: a meta-analysis.两种 BER 基因多态性与乳腺癌风险之间缺乏关联:一项荟萃分析。
PLoS One. 2012;7(12):e50857. doi: 10.1371/journal.pone.0050857. Epub 2012 Dec 14.
8
Racial and tissue-specific cancer risk associated with PARP1 (ADPRT) Val762Ala polymorphism: a meta-analysis.PARP1(ADPRT)Val762Ala 多态性与种族和组织特异性癌症风险的关联:一项荟萃分析。
Mol Biol Rep. 2012 Dec;39(12):11061-72. doi: 10.1007/s11033-012-2009-x. Epub 2012 Oct 17.
9
Correlation between base-excision repair gene polymorphisms and levels of in-vitro BPDE-induced DNA adducts in cultured peripheral blood lymphocytes.碱基切除修复基因多态性与体外 BPDE 诱导的培养外周血淋巴细胞 DNA 加合物水平的相关性。
PLoS One. 2012;7(7):e40131. doi: 10.1371/journal.pone.0040131. Epub 2012 Jul 5.
10
Association between PARP-1 V762A polymorphism and cancer susceptibility: a meta-analysis.PARP-1 V762A 多态性与癌症易感性的关联:一项荟萃分析。
Genet Epidemiol. 2012 Jan;36(1):56-65. doi: 10.1002/gepi.20663. Epub 2011 Nov 29.
人类乳腺癌风险中DNA修复基因多态性的多基因模型。
Carcinogenesis. 2008 Nov;29(11):2132-8. doi: 10.1093/carcin/bgn193. Epub 2008 Aug 13.
4
High-resolution melt curve analysis: initial screening for mutations in BCR-ABL kinase domain.高分辨率熔解曲线分析:BCR-ABL激酶结构域突变的初步筛查
Leuk Res. 2008 Aug;32(8):1236-43. doi: 10.1016/j.leukres.2008.01.010. Epub 2008 Mar 4.
5
Genetic polymorphisms in DNA base-excision repair genes ADPRT, XRCC1, and APE1 and the risk of squamous cell carcinoma of the head and neck.DNA碱基切除修复基因ADPRT、XRCC1和APE1的基因多态性与头颈部鳞状细胞癌风险
Cancer. 2007 Aug 15;110(4):867-75. doi: 10.1002/cncr.22861.
6
Polymorphisms involved in the folate metabolizing pathway and risk of multiple myeloma.叶酸代谢途径中的多态性与多发性骨髓瘤风险
Am J Hematol. 2007 Sep;82(9):798-801. doi: 10.1002/ajh.20967.
7
Genetic variation in the base excision repair pathway and bladder cancer risk.碱基切除修复途径中的基因变异与膀胱癌风险
Hum Genet. 2007 Apr;121(2):233-42. doi: 10.1007/s00439-006-0294-y. Epub 2007 Jan 3.
8
Polymorphisms in DNA repair genes and risk of non-Hodgkin lymphoma among women in Connecticut.康涅狄格州女性DNA修复基因多态性与非霍奇金淋巴瘤风险
Hum Genet. 2006 Jul;119(6):659-68. doi: 10.1007/s00439-006-0177-2. Epub 2006 Apr 26.
9
[Correlation of genetic polymorphisms in DNA repair genes ADPRT and XRCC1 to risk of gastric cancer].[DNA修复基因ADPRT和XRCC1的基因多态性与胃癌风险的相关性]
Ai Zheng. 2006 Jan;25(1):7-10.
10
Gender differences in the endotoxin-induced inflammatory and vascular responses: potential role of poly(ADP-ribose) polymerase activation.内毒素诱导的炎症和血管反应中的性别差异:聚(ADP - 核糖)聚合酶激活的潜在作用。
J Pharmacol Exp Ther. 2005 Nov;315(2):812-20. doi: 10.1124/jpet.105.090480. Epub 2005 Aug 3.