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MKK4基因启动子区-1304T>G多态与食管癌易感性研究 被引量:5

No association between the functional polymorphism(-1304T>G) in the MKK4 gene and the risk of esophageal cancer
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摘要 目的:探讨MKK4基因-1304T>G位点单核苷酸多态基因型在中国东部人群中的分布及其对食管癌易感性的影响。方法:设计以医院为基础的病例对照研究,进行食管癌患者与对照人群频数匹配,采用聚合酶链反应-限制性片段长度多态性的方法(PCR-RFLP)对571例食管癌患者和785名正常人的MKK4基因-1304T>G位点(rs3826392)进行基因分型。利用Logistic回归分析基因多态性与食管癌发病风险的关联,并校正年龄和性别。结果:MKK4基因-1304T>G位点基因多态性在病例和对照组中分布差异无统计学意义,GG基因型(OR=0.98,95%CI:0.67~1.61),TG基因型(OR=1.12,95%CI:0.90~1.43),P=0.435。结论:MKK4基因-1304T>G位点的单核苷酸多态可能与中国东部人群食管癌易感性无关。 OBJECTIVE: To detect the association between the functional polymorphism (-1304T〉 G) of the MKK4 gene and the risk of esophageal cancer in Eastern Chinese population. METHODS: A hospital based case-control study was carried out in Eastern Chinese populations, totally contain 571 esophageal cancer patients and 785 age and sex matched controls by using polymerase chain reaction-restriction fragment length polymorphism (PCR RFLP) method. RESULTS: No significant association was observed between the -1304T〉G polymorphism genotypes and esophageal cancer risk (GG: OR=0.98,95%CI:0.67-1.61; TG: OR=1. 12, 95%CI:0. 90-1. 43; P=0. 435). CONCLUSION: It suggests that the genetic variant MKK4 -1304T〉 G may not as a causative factor for the susceptibility of esophageal cancer in Eastern Chinese population.
出处 《中华肿瘤防治杂志》 CAS 北大核心 2012年第2期88-91,共4页 Chinese Journal of Cancer Prevention and Treatment
基金 国家自然科学基金面上项目(81171895)
关键词 食管癌 MKK4 基因多态性 esophageal neoplasms MKK4 polymorphisms
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  • 1Kyle J Napier,Mary Scheerer,Subhasis Misra.Esophageal cancer: A Review of epidemiology, pathogenesis, staging workup and treatment modalities[J].World Journal of Gastrointestinal Oncology,2014,6(5):112-120. 被引量:97
  • 2周彩虹,黄启福.凋亡与肿瘤及其治疗进展[J].中国病理生理杂志,2004,20(11):2124-2133. 被引量:16
  • 3柴立勋,孙克林,郭黎平,张宏图,陆士新.食管鳞癌中Ezrin和CD44-v6的表达及其临床意义[J].中华肿瘤杂志,2007,29(9):685-688. 被引量:26
  • 4Dong SW,Cui YT,Zhong RR,et al. Decreased expression of retinoblastoma protein-interacting zinc-finger gene 1 in human esophageal squamous cell cancer by DNA methylation [J]. Clin Lab,2012,58(1-2) :41-51.
  • 5Nie GY,Hampton A ,Li Y,et al. Identification and cloning of two isoforms of human high-temperature requirement factor A3 (HtrA3), characterization of its genomic structure and comparison of its tissue distribution with HtrA1 and HtrA2[J]. Bioehem J, 2003,371 (Pt 1 ) : 39-48.
  • 6Garrido C, Kroemer G. Life's smile ,death's grin :vital functions of apoptosis-executing proteins[J]. Curr Opin Cell Biol,2004,16 (6) : 639-646.
  • 7Verhagen AM ,Silke J ,Ekert PG,et al. HtrAZ promotes ceil aeam through its serine protease activity and its ability to antagonize inhibitor of apoptosis proteins[J]. J Biol Chem,2002,277 (1): 445-454.
  • 8Hegde R,Srinivasula SM,Zhang Z,et al. Identification of Omi/ HtrA2 as a mitochondrial apoptotic serine protease that disntpts inhibitor of apoptosis protein-caspase interaction[J]. J Biol Chem, 2002,277 (1) : 432-438.
  • 9Winkler J,Rand ML,Schmugge M,et al. Omi/HtrA2 and XIAP are components of platelet apoptosis signalling[J]. Thromb Haemost, 2013,109(3) :532-539.
  • 10CHEN L, HU C S, CHEN X Z, et al. Concurrent chemoradiotherapy plus adjuvant chemotherapy versus concurrent chemoradiotherapy alone in patients with locoregionally advanced nasopharyngeal carcinoma: a phase 3 multicentre randomised controlled trial[J]. Lancet Oncol, 2012,13.163--171.

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