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家族史阳性和阴性食管癌患者癌组织中FHIT和BRCA2及MLH1的表达变化
引用本文:常志伟,王立东,王宁博,王苒,江亚南,杜芳,齐义军,郭涛,孙哲,李吉林,常扶保,常志军,郭海云,未庆丽,范宗民,高珊珊,何欣,郭花芹.家族史阳性和阴性食管癌患者癌组织中FHIT和BRCA2及MLH1的表达变化[J].中华肿瘤防治杂志,2006,13(18):1371-1374.
作者姓名:常志伟  王立东  王宁博  王苒  江亚南  杜芳  齐义军  郭涛  孙哲  李吉林  常扶保  常志军  郭海云  未庆丽  范宗民  高珊珊  何欣  郭花芹
作者单位:1. 河南省食管癌重点开放实验室,郑州大学医学实验中心癌症研究室,郑州大学第一附属医院消化内科,河南,郑州,450052
2. 林州市姚村食管癌医院病理科,河南,林州,456592
3. 林州市中心医院外科,河南,林州,456550
基金项目:国家杰出青年科学基金(30025016),河南省医学科技攻关(20058),河南省高校创新人才工程基金(1999125),河南省食管癌重点开放实验室基金(20050227),郑州大学211工程项目
摘    要:目的:探讨FHIT、BRCA2及MLH1在河南食管癌高发区家族史阳、阴性食管癌患者癌组织中的表达变化,及其与食管癌遗传易感性之间的关系。方法:采用ABC法检测河南省食管癌高发区林州市74例食管癌患者(其中33例家族史阳性,41例家族史阴性)手术切除标本癌组织FHIT、BRCA2及MLH1蛋白表达情况。结果:FHIT56%(18/33)]、BRCA267%(22/33)]和MLH173%(24/33)]在家族史阳性食管癌患者癌组织中阴性表达率,显著高于家族史阴性食管癌患者27%(11/41)、37%(15/44)和27%(16/41)],P值均<0·05。结论:FHIT、BRCA2和MLH1蛋白可能是影响食管癌遗传易感性的重要分子事件之一。

关 键 词:食管肿瘤  疾病遗传易感性  蛋白质类  近亲
文章编号:1673-5269(2006)18-1371-04
收稿时间:2005-12-05
修稿时间:2006-03-30

Alterations of FHIT, BRCA2 and MLH1 expressions in esophageal cancer tissues from the esophageal cancer patients with and without family history
CHANG Zhi-wei,WANG Li-dong,WANG Ning-bo,WANG Ran,JIANG Ya-nan,DU Fang,QI Yi-jun,GUO Tao,SUN Zhe,LI Ji-lin,CHANG Fu-bao,CHANG Zhi-jun,GUO Hai-yun,WEI Qin-li,FAN Zong-min,GAO Shan-shan,HE Xin,GUO Hua-qin.Alterations of FHIT, BRCA2 and MLH1 expressions in esophageal cancer tissues from the esophageal cancer patients with and without family history[J].Chinese Journal of Cancer Prevention and Treatment,2006,13(18):1371-1374.
Authors:CHANG Zhi-wei  WANG Li-dong  WANG Ning-bo  WANG Ran  JIANG Ya-nan  DU Fang  QI Yi-jun  GUO Tao  SUN Zhe  LI Ji-lin  CHANG Fu-bao  CHANG Zhi-jun  GUO Hai-yun  WEI Qin-li  FAN Zong-min  GAO Shan-shan  HE Xin  GUO Hua-qin
Abstract:OBJECTIVE:To explore the alterations of FHIT,BRCA2 and MLH1 expressions in esophageal cancer (EC) tissues from the patients with and without EC familial history at a high-incidence area for EC in Henan Province, and to correlate these changes with EC hereditary susceptibility. METHODS:The immunohistochemical method (ABC) and histopathological method were applied to test 74 EC specimens and the expressions of FHIT,BRCA2 and MLH1 proteins in SCC were correlated with the hereditary susceptibility distribution. Thirty-three of the 74 EC specimens were from the families which had two or more EC patients in continuous two generations (positive EC family history, ECFH ) and 41 specimens were from the families without positive tumor history (ECFH-). RESULTS:The negative expression of FHIT gene was significantly higher in ECFH (56%,18/33) than that in ECFH-(27%,11/41, P< 0.05). The negative expression of BRCA2 gene was significantly higher in EC tissue from the ECFH than that from the ECFH-67%( 22/33 ) vs 37%(15/41),P<0.05). The negative expression rate for MLH1 in the ECFH (73%,24/33) was higher than that in the ECFH-(27%, 16/41 ), P< 0.01.CONCLUSION:FHIT,BRCA2 and MLH1 may play an important role in the EC familial hereditary susceptibility.
Keywords:esophageal neoplasms  genetic predisposeitim to disease  proteins  consanguinity
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