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作 者:张晓云[1] 张春雁[2] 孙曼萍[1] 王雨稼[1] 李棣华[1]
机构地区:[1]上海中医药大学附属岳阳中西医结合医院病理科,上海200437 [2]上海中医药大学
出 处:《中国临床医学》2008年第2期189-192,共4页Chinese Journal of Clinical Medicine
基 金:上海中医药大学附属岳阳中西医结合医院院级科研项目
摘 要:目的:探讨脆性组氨酸三联体(FHIT)和β-连接素(β-catenin)蛋白在大肠癌中的表达及其临床病理学意义。方法:采用免疫组织化学EnVision两步法,检测76例大肠癌及癌周非瘤粘膜组织、30例腺瘤标本的FHIT和β-catenin表达。结果:腺癌组织中FHIT表达降低或缺失率为51.3%,明显高于腺瘤组(6.7%)(P<0.01)。在癌的组织学分级中显示高分化组占10%,与中分化(56%)或低分化组(62.5%)相比差异显著(P<0.05)。大肠癌、大肠腺瘤组织中β-catenin的异常表达率分别为86.8%、73.3%,均显著高于癌旁非瘤黏膜组织(0%)(P<0.01)。在肿瘤的组织学分级中,β-catenin的异常表达率在中、低分化组为90.9%,显著高于高分化组(60%)(P<0.05);在临床分期中,DukesC及D期的β-catenin异常表达率为95.7%,显著高于DukesA及B期(72.4%)(P<0.01);伴淋巴结转移的β-catenin的异常表达率为95.3%,显著高于无淋巴结转移(75.8%)(P<0.05)。β-catenin异常表达与FHIT表达降低或缺失之间呈显著正相关关系(r=0.244,P<0.05)。结论:FHIT表达降低或缺失及其β-catenin的异常表达在大肠癌的发生发展中起重要作用。部分大肠癌组织中β-catenin的异常表达可能由抑癌基因FHIT的表达降低或缺失所致。Objective:To investigate the expression of fragile histidine triad (FHIT) and β-catenin protein and their correlations with clinicopathologic features in colorectal carcinomas. Methods:The expression of FHIT and β-catenin protein was investigated in 76 primary colorectal carcinomas, adjacent noncancerous mucosa and 30 adenomas using EnVision immunohistochemistry. Results.. The reduction or loss rate of FHIT expression was 51.3 % in colorectal carcinomas, and significantly higher than that in adenomas (6.70%) (P〈0.01): 10% well-differentiated, 56%moderately-differentiated, 62.5%poorly-differentiated carcinomas, the frequency being significantly higher in the latter two than that in the former (P〈0.05). The abnormal expression rate of β-catenin was 86.8%, 73.3 % in colorectal carcinomas and adenomas respectively. They were significantly higher than that in adjacent noncancerous mucosa(0~) (P%0.01). The abnormal expression rate of β-catenin was significantly higher in moderately and poorly-differentiated carcinomas(90.9% ) than that in well-differentiated carcinomas(60% ) (P〈0. 05). It was also significantly higher in late stage carcinomas(Dukes stage C + D) (95.7%) (P〈0.01) and carcinomas with lymph node metastasis(95.3%) (P〈0.05). The abnormal expression of β-catenin was in positive correlation with the reduction or loss expression of FHIT(r = 0. 244, P〈0.05). Conclusion . The abnormal expression of β-catenin and the reduction or loss expression of FHIT play important roles in the carcinogenesis and progression of colorectal carcinoma. The abnormal expression of β-catenin may be induced by the reduction or loss expression of FHIT in some colorectal carcinomas.
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