期刊文献+

乙醛脱氢酶与人类疾病的相互关系研究进展 被引量:1

Research Progress in the Relationship between Aldehyde Dehydrogenase and Human Diseases
下载PDF
导出
摘要 乙醛脱氢酶(acetaldehyde dehydrogenase,ALDH)是人体重要的醛脱氢酶之一,催化体内乙醛氧化为乙酸。在组织细胞中,ALDH能解除醛基的毒害作用,其活性的高低与多种人类疾病密切相关。ALDH主要有ALDH1和ALDH2两种同工酶:ALDH1与多种肿瘤的发生发展及预后有紧密联系,在乳腺癌、结直肠癌及肺癌等疾病中均存在高表达现象;ALDH2的基因多态性在亚洲人中多见,除了与消化道肿瘤、酒精性肝病等消化道疾病息息相关,还与心肌梗死、帕金森病(PD)、白血病等密切相关。近年来,关于ALDH的研究日益增多,现就ALDH与人类疾病之间相互关系的研究现状作一综述。 Aldehyde dehydrogenase(ALDH) is one of the important human aldehyde dehydrogenase catalyzing the oxidation of acetaldehyde to acetic acid in vivo. ALDH can eliminate the toxic effects of aldehyde in tissue cells and its activity is closely related to various human diseases.There are two kinds of ALDH isozymes: ALDH1 and ALDH2. ALDH1 is associated with the development and the prognosis of various tumors and highly expressed in breast cancer, colorectal cancer and lung cancer. Polymorphism of ALDH2 is more common in Asians. In addition to gastrointestinal cancer, alcoholic liver disease and other gastrointestinal diseases, ALDH2 is closely related to myocardial infarction, Parkinson's disease(PD), leukemia and other diseases. In recent years, there are more and more researches on the relationship between ALDH and human diseases. In this paper, the research progress in their relationship was reviewed and summarized.
出处 《酿酒科技》 北大核心 2014年第10期89-91,共3页 Liquor-Making Science & Technology
基金 国家基础医学人才培养基地--能力提高项目(编号J1103604)
关键词 ALDH 疾病 肿瘤 饮酒与健康 ALDH disease tumor drinking and health
  • 相关文献

参考文献11

二级参考文献73

  • 1丁建华,吴建中,高长明,李苏平,周建农,曹海霞,苏平,周学富,丁保国,王如鸿.乙醛脱氢酶2基因多态性和饮酒习惯与肝癌的易感性[J].肿瘤,2004,24(4):309-312. 被引量:16
  • 2沈海幸,付颖,袁杨,邸亚丽,付强,张开立,马景昕,李宏.细胞色素P4501 A1基因多态性与胃癌易感性的研究[J].大连医科大学学报,2005,27(1):22-24. 被引量:4
  • 3Chia-Fang Wu,Deng-Chyang Wu,Hon-Ki Hsu,Ein-Long Kao,Jang-Ming Lee,Cheng-Chieh Lin,Ming-Tsang Wu.Relationship between genetic polymorphisms of alcohol and aldehyde dehydrogenases and esophageal squamous cell carcinoma risk in males[J].World Journal of Gastroenterology,2005,11(33):5103-5108. 被引量:7
  • 4[1]Schoffner J,Wallace DC.Heart disease and mitochondrial DNA mutations.Heart Dis Stroke,1992,1 (4):235-238
  • 5[3]Murray J,Gilkerson R,Capaldi RA.Quantitative proteomics:the copy number of pyruvate dehydrogenase is more than 10(2)-fold lower than that of complex Ⅲ in human mitochondria.Febs Lett,2002,529 (2-3):173-178
  • 6[4]Kernec F,Unlu M,Labeikovsky W,Minden JS,Koretsky AP.Changes in the mitochondrial proteome from mouse hearts deficient in creatine kinase.Physiol Genomics,2001,6 (2):117-128
  • 7[5]Rabilloud T,Kieffer S,Procaccio V,Louwagie M,Courchesne PL,Patterson SD,et al.Two-dimensional electrophoresis of human placental mitochondria and protein identification by mass spectrometry:Toward a human mitochondrial proteome.Electrophoresis,1998,19 (6):1 006-014
  • 8[7]Aebersold R,Goodlett DR.Mass spectrometry in proteomics.Chem Rev,2001,101 (2):269-295
  • 9[8]Ferguson RA,Goldberg DM.Genetic markers of alcolol abuse.J Clin Chim Acta,1997,257 (2):199-250
  • 10[9]Watanabe S,Sasahara K,Kinekawa F,Uchida N,Masaki T,Kurokohchi K,et al.Aldehyde dehydrogenase-2 genotypes and HLA haplotypes in Japanese patients with esophageal cancer.Oncol Rep,2002,9 (5):1 063-068

共引文献74

同被引文献30

引证文献1

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部