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胃癌及胃癌前病变中APC、bcl-2和c-met基因的表达及意义
引用本文:陆以霞,祝喜萍,卢艳红,迟宝荣.胃癌及胃癌前病变中APC、bcl-2和c-met基因的表达及意义[J].吉林大学学报(医学版),2007,33(2):314-317.
作者姓名:陆以霞  祝喜萍  卢艳红  迟宝荣
作者单位:1.吉林大学第一医院消化内科,吉林 长春 130021;2.黑龙江省医院消化内科,黑龙江 哈尔滨 150001;3.黑龙江省医院病理科,黑龙江 哈尔滨 150001
摘    要:目的:探讨APC、bcl-2和c-met基因在胃癌发生、发展中的作用以及在胃癌早期诊断中的意义。方法:应用免疫组化技术检测APC、bcl-2、c-met蛋白在30例胃癌、30例不典型增生、30例肠上皮化生(肠化)、10例胃腺瘤及20例正常胃黏膜组织中的表达。结果: ①APC 阳性表达率在肠化、不典型增生、胃癌及胃腺瘤组织中表达率分别为66.7%、53.3%、53.3%和50.0%,与正常胃黏膜组织(90.0%)比较明显降低(P<0.05),其中中重度不典型增生APC表达率(47.1%)低于轻度不典型增生(61.5%)(P<0.05)。APC在无淋巴结转移的胃癌组织中表达率高于有淋巴结转移的胃癌组织(P<0.05)。② bcl-2阳性表达率在胃癌(66.7%)、不典型增生(43.3%)、肠化(40.0%)胃黏膜组织中表达率均明显高于正常对照组(5.0%)和胃腺瘤组(10.0%)(P<0.05);轻度不典型增生组阳性表达率(30.8%)低于胃癌组 (P<0.05);中重度不典型增生组(52.9%)与胃癌组比较差异无显著性 (P>0.05)。中高分化胃癌组织中bcl-2表达率者高于低分化者(P<0.05), Lauren分型肠型胃癌中表达率高于弥漫型(P<0.05)。③ c-met阳性表达率在胃癌(63.3%)、肠化(63.3%)和不典型增生组织(60.0%)均明显高于正常胃黏膜组(10.0%)和胃腺瘤组(10.0%)(P<0.05);中重度不典型增生组阳性表达率(70.6%)明显高于轻度不典型增生组(46.1%)(P<0.05);中重度肠化组阳性表达率(75.0%)明显高于轻度肠化组(55.6%)(P<0.05)。中高分化胃癌c-met阳性表达率高于低分化胃癌(P<0.05),有淋巴结转移者高于无淋巴结转移者(P<0.05)。结论:APC基因的失活、bcl-2和c-met基因的过表达对胃癌的发生、发展起促进作用;对中重度不典型增生胃黏膜进行APC、bcl-2和c-met基因检测有助于胃癌的早期诊断。

关 键 词:癌前状态    基因  APC    基因    bcl-2    原癌基因蛋白质  c-met    免疫组织化学    
文章编号:1671-587X(2007)02-0314-04
收稿时间:2006-10-18
修稿时间:2006年10月18日

Expressions of APC, bcl-2 and c-met in gastric cancer and its precancerous lesion and their significances
LU Yi-xia,ZHU Xi-ping,LU Yan-hong,CHI Bao-rong.Expressions of APC, bcl-2 and c-met in gastric cancer and its precancerous lesion and their significances[J].Journal of Jilin University: Med Ed,2007,33(2):314-317.
Authors:LU Yi-xia  ZHU Xi-ping  LU Yan-hong  CHI Bao-rong
Institution:1.Department of Digestive Medicine, First Hospital, Jilin University, Changchun 130021,China;2.Department of Digestive Medicine, Heilongjiang Province Hospital, Haerbin 150001, China;3.Department of Pathology,Heilongjiang Province Hospital, Haerbin 150001,
Abstract:Objective To investigate the role of the expressions of APC,bcl-2 and c-met gene in the progress of gastric cancer and their significances in the diagnosis of early gastric cancer.Methods The immunohistochemical technique was used to detect the expressions of APC,bcl-2 and c-met gene in 30 cases of human gastric carcinoma(GC),30 cases of intestinal metaplasia(IM),30 dysplasia(Dys) gastric mucosa,10 gastric adenoma(GA) and 20 normal gastric mucosa.Results ①The positive expression rates of APC in GC,IM,Dys and GA(53.3%,67.7% and 53.3%,respectively) were significantly lower than those in normal gastric mucosa(90.0%,P<0.05).The positive rate of APC in moderate and severe Dys(47.1%) was lower than that in mild Dys(61.5%,P<0.05).The expression rate of APC in GC without lymph node metastasis was higher than those with lymph node metastasis(P<0.05).②The positive expression rates of bcl-2 in GC(66.7%),IM(40.0%) and Dys(43.3%)were higher than those in normal gastric mucosa(5.0%) and GA(10.0%).The positive expression rate of bcl-2 in mild Dys(30.8%) was lower than those in GC(66.7%,P<0.05).The bcl-2 expression showed a significant negative correlation with lymph node metastasis and Lauren type(P<0.05).③The positive expression rates of c-met in GC(76.0%),IM(63.3%) and Dys(60.0%) were higher than those in normal gastric mucosa(10.0%,P<0.05)) and gastric adenoma(10.0%,P<0.05).The positive expression rate of c-met in moderate and severe IM(70.6%)was higher than those in mild IM(46.1%,P<0.05).The positive expression rate of c-met in moderate and severe Dys(75%) was higher than that in mild Dys(55.6%,P<0.05).The expression of c-met gene in GC with well differentiation was higher than that with bad differentiation(P<0.05).The expression of c-met gene in GC with lymph node metastasis was higher than that without lymph node metastasis(P<0.05).Conclusion The lose of APC or bcl-2 and c-met gene overexpression are contributed to the occurance and development of GC.To detect the expressions of APC,bcl-2 and c-met gene in moderate and severe Dys may be helpful for diagnosis of early gastric cancer.
Keywords:gastric neoplasms  precancerous conditions  genes  APC  genes  bcl-2  proto-oncogene protein c-met  immunohistochemistry
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