• 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

p53 密码子 72 多态性与冠状动脉疾病:与 ACP₁ 相互作用的证据。

p53 codon 72 polymorphism and coronary artery disease: evidence of interaction with ACP₁.

机构信息

Department of Biopathology and Imaging Diagnostics, University of Rome Tor Vergata, Rome, Italy.

出版信息

Med Sci Monit. 2012 Dec;18(12):CR712-5. doi: 10.12659/msm.883597.

DOI:10.12659/msm.883597
PMID:23197232
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3560788/
Abstract

BACKGROUND

Common biological features between cancer and atherosclerosis suggest possible association of p53 with atherosclerotic diseases, but data on such a relationship are controversial, suggesting interactions with other variables. Acid phosphatase locus 1 (ACPACP₁) is a polymorphic gene that controls the synthesis of an enzyme involved in important metabolic functions. Since ACPACP₁ is associated with coronary artery disease (CAD), we searched for possible interactions between this enzyme and p53 codon 72 polymorphism with regard to their effects on susceptibility to CAD.

MATERIAL/METHODS: The study included 381 patients admitted to the hospital for cardiovascular disease (232 patients with CAD and 149 with other cardiovascular problems) and 97 healthy newborns.

RESULTS

The proportion of subjects carrying the *Pro allele of p53 codon 72 and the high activity BC genotype of ACPACP₁ is higher in CAD (10.3%) than in non-CAD patients (2.0%) and in healthy newborns (6.2%).

CONCLUSIONS

The data suggest an interaction between p53 codon 72 and ACPACP₁ wherein a positive effect of the p53 *Pro allele on susceptibility to CAD occurs, but only in the presence of the ACPACP₁ genotype characterized by high enzymatic activity.

摘要

背景

癌症和动脉粥样硬化之间存在共同的生物学特征,这表明 p53 可能与动脉粥样硬化疾病有关,但关于这种关系的数据存在争议,表明其与其他变量存在相互作用。酸性磷酸酶基因座 1(ACPACP₁)是一种多态性基因,控制着参与重要代谢功能的酶的合成。由于 ACPACP₁与冠心病(CAD)有关,我们搜索了这种酶与 p53 密码子 72 多态性之间可能存在的相互作用,以研究它们对 CAD 易感性的影响。

材料/方法:该研究纳入了 381 名因心血管疾病住院的患者(232 名 CAD 患者和 149 名其他心血管问题患者)和 97 名健康新生儿。

结果

携带 p53 密码子 72 的Pro 等位基因和 ACPACP₁高活性B*C 基因型的受试者在 CAD 患者(10.3%)中的比例高于非 CAD 患者(2.0%)和健康新生儿(6.2%)。

结论

数据表明 p53 密码子 72 与 ACPACP₁ 之间存在相互作用,其中 p53*Pro 等位基因对 CAD 的易感性有正向影响,但仅在 ACPACP₁ 基因型具有高酶活性的情况下才会发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b087/3560788/6df7701b772b/medscimonit-18-12-CR712-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b087/3560788/6df7701b772b/medscimonit-18-12-CR712-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b087/3560788/6df7701b772b/medscimonit-18-12-CR712-g001.jpg

相似文献

1
p53 codon 72 polymorphism and coronary artery disease: evidence of interaction with ACP₁.p53 密码子 72 多态性与冠状动脉疾病:与 ACP₁ 相互作用的证据。
Med Sci Monit. 2012 Dec;18(12):CR712-5. doi: 10.12659/msm.883597.
2
Coronary artery disease: evidence of interaction between PTPN22 and p53 genetic polymorphisms.冠状动脉疾病:PTPN22与p53基因多态性之间相互作用的证据。
Cardiology. 2011;120(3):166-8. doi: 10.1159/000334808. Epub 2011 Dec 29.
3
The Arg72 variant of the p53 functional polymorphism (rs1042522) is associated with coronary artery disease in young South Africans of Indian ancestry.p53功能多态性(rs1042522)的Arg72变体与印度裔南非年轻人的冠状动脉疾病有关。
Gene. 2016 Nov 30;593(2):261-4. doi: 10.1016/j.gene.2016.07.040. Epub 2016 Jul 17.
4
p53 codon 72 polymorphism and coronary artery disease: evidence of association with left ventricular ejection fraction.p53 密码子 72 多态性与冠状动脉疾病:与左心室射血分数相关的证据。
Am J Med Sci. 2012 Feb;343(2):127-130. doi: 10.1097/MAJ.0b013e318223ac71.
5
The effect of ACP1, ADA6 and PTPN22 genetic polymorphisms on the association between p53 codon 72 polymorphism and endometriosis.ACP1、ADA6和PTPN22基因多态性对p53密码子72多态性与子宫内膜异位症之间关联的影响。
Arch Gynecol Obstet. 2016 Feb;293(2):399-402. doi: 10.1007/s00404-015-3827-6. Epub 2015 Jul 28.
6
Interaction between p53 codon 72 and MDM2 309T>G polymorphisms and the risk of hepatocellular carcinoma.p53密码子72与MDM2 309T>G多态性之间的相互作用及肝细胞癌风险
Tumour Biol. 2016 Mar;37(3):3863-70. doi: 10.1007/s13277-015-4222-4. Epub 2015 Oct 17.
7
Polymorphism of p53 gene codon 72 in Kuwaiti with coronary artery disease and diabetes.科威特冠心病和糖尿病患者中p53基因密码子72的多态性
Int J Cardiol. 2007 Jan 31;115(1):1-6. doi: 10.1016/j.ijcard.2006.01.029. Epub 2006 Jun 23.
8
ACP1 genetic polymorphism and coronary artery disease: an association study.ACP1基因多态性与冠状动脉疾病:一项关联研究。
Cardiology. 2009;113(4):236-42. doi: 10.1159/000203405. Epub 2009 Feb 25.
9
Association of p53 codon 72 genetic polymorphism with the risk of ulcerative colitis in northern Iran.p53 密码子 72 遗传多态性与伊朗北部溃疡性结肠炎发病风险的关联。
Int J Colorectal Dis. 2011 Feb;26(2):235-8. doi: 10.1007/s00384-010-1021-7. Epub 2010 Jul 29.
10
Meta-analysis of an association of codon 72 polymorphisms of the p53 gene with increased endometrial cancer risk.p53基因密码子72多态性与子宫内膜癌风险增加相关性的Meta分析。
Genet Mol Res. 2011 Oct 31;10(4):3609-19. doi: 10.4238/2011.October.31.11.

引用本文的文献

1
The association between peroxisome proliferator-activated receptor Δ rs3777744, rs3798343, and rs6922548 and coronary artery disease.过氧化物酶体增殖物激活受体 Δ rs3777744、rs3798343 和 rs6922548 与冠状动脉疾病的相关性。
Biosci Rep. 2019 Jan 3;39(1). doi: 10.1042/BSR20181510. Print 2019 Jan 31.
2
TP53 single nucleotide polymorphism (rs1042522) in Iranian patients with coronary artery disease.伊朗冠心病患者的TP53单核苷酸多态性(rs1042522)
Biomed Rep. 2018 Sep;9(3):259-265. doi: 10.3892/br.2018.1121. Epub 2018 Jul 2.
3
Association of P53 gene polymorphism with gastric cancer in Northern Iran as a high-risk region.

本文引用的文献

1
Application of a multiplex SNP genotyping system in predicting genetic susceptibility to CAD in Chinese people of Han ethnicity.多重 SNP 基因分型系统在预测汉族中国人 CAD 遗传易感性中的应用。
Med Sci Monit. 2010 Dec;16(12):BR384-95.
2
Apoptosis of CD4+ CD25(high) T cells in type 1 diabetes may be partially mediated by IL-2 deprivation.1 型糖尿病中 CD4+ CD25(high) T 细胞的凋亡可能部分由 IL-2 剥夺介导。
PLoS One. 2009 Aug 5;4(8):e6527. doi: 10.1371/journal.pone.0006527.
3
ACP1 genetic polymorphism and coronary artery disease: an association study.
伊朗北部作为高风险地区P53基因多态性与胃癌的关联
Biomed Rep. 2018 May;8(5):433-438. doi: 10.3892/br.2018.1070. Epub 2018 Feb 22.
4
Association Between Paraoxonase 2 Ser311Cys Polymorphism and Coronary Heart Disease Risk: A Meta-Analysis.对氧磷酶2基因Ser311Cys多态性与冠心病风险的关联:一项荟萃分析。
Med Sci Monit. 2016 Sep 9;22:3196-201. doi: 10.12659/msm.896601.
5
Intercellular adhesion molecule-1 K469E polymorphism and risk of coronary artery disease: a meta-analysis.细胞间黏附分子-1 K469E 多态性与冠心病风险的关系:一项荟萃分析。
Med Sci Monit. 2014 Dec 15;20:2677-82. doi: 10.12659/MSM.891235.
6
Meta-analysis of Ubiquilin1 gene polymorphism and Alzheimer's disease risk.泛素连接酶1基因多态性与阿尔茨海默病风险的荟萃分析。
Med Sci Monit. 2014 Nov 12;20:2250-5. doi: 10.12659/MSM.891030.
7
The OSR1 rs12329305 polymorphism contributes to the development of congenital malformations in cases of stillborn/neonatal death.OSR1基因rs12329305多态性在死产/新生儿死亡病例中对先天性畸形的发生有影响。
Med Sci Monit. 2014 Aug 28;20:1531-8. doi: 10.12659/MSM.890916.
8
Association between phosphatase related gene variants and coronary artery disease: case-control study and meta-analysis.磷酸酶相关基因变异与冠状动脉疾病之间的关联:病例对照研究与荟萃分析。
Int J Mol Sci. 2014 Aug 13;15(8):14058-76. doi: 10.3390/ijms150814058.
ACP1基因多态性与冠状动脉疾病:一项关联研究。
Cardiology. 2009;113(4):236-42. doi: 10.1159/000203405. Epub 2009 Feb 25.
4
Polymorphism of p53 gene codon 72 in Kuwaiti with coronary artery disease and diabetes.科威特冠心病和糖尿病患者中p53基因密码子72的多态性
Int J Cardiol. 2007 Jan 31;115(1):1-6. doi: 10.1016/j.ijcard.2006.01.029. Epub 2006 Jun 23.
5
Serum glucose concentration and ACP1 genotype in healthy adult subjects.健康成年受试者的血清葡萄糖浓度与ACP1基因型
Metabolism. 2005 Jul;54(7):891-4. doi: 10.1016/j.metabol.2005.02.002.
6
Tumor suppressor p53 inhibits autoimmune inflammation and macrophage function.
Diabetes. 2005 May;54(5):1423-8. doi: 10.2337/diabetes.54.5.1423.
7
P53 codon 72 polymorphism in coronary artery disease: no evidence for association with increased risk or micronucleus frequency.冠状动脉疾病中P53密码子72多态性:无证据表明与风险增加或微核频率相关。
Environ Mol Mutagen. 2002;40(2):110-5. doi: 10.1002/em.10098.
8
Low-molecular-weight protein tyrosine phosphatase and human disease: in search of biochemical mechanisms.
Arch Immunol Ther Exp (Warsz). 2002;50(2):95-104.
9
Activation of ZAP-70 through specific dephosphorylation at the inhibitory Tyr-292 by the low molecular weight phosphotyrosine phosphatase (LMPTP).低分子量磷酸酪氨酸磷酸酶(LMPTP)通过对抑制性酪氨酸292进行特异性去磷酸化来激活ZAP-70。
J Biol Chem. 2002 Jul 5;277(27):24220-4. doi: 10.1074/jbc.M202885200. Epub 2002 Apr 25.
10
Evidence for DNA damage in patients with coronary artery disease.冠状动脉疾病患者DNA损伤的证据。
Mutat Res. 2001 Jun 27;493(1-2):23-30. doi: 10.1016/s1383-5718(01)00162-0.