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出 处:《医学分子生物学杂志》2011年第3期253-256,共4页Journal of Medical Molecular Biology
摘 要:目的 检测p-MAPK、CyclinD1和CDK4蛋白在大肠癌中的表达,并探讨其相关性.方法 选取78例大肠癌组织,距癌灶3 cm以外的癌旁组织,进行组织切片,HE染色进行病理分型,应用S-P免疫组化法对组织中的p-MAPK、Cyclin D1和CDK4进行检测.结果 病理分型后,78例大肠癌中p-MAPK、CyclinD1和CDK4蛋白的阳性表达率分别为67.9 %(53/78)、57.7 %(45/78)和39.7 %(31/78);78例相应癌旁组织中阳性表达率分别为6.4 %(5/78)、10.3 %(8/78)和19.2 %(15/78).三者阳性表达率和阳性强度均以大肠癌中为高(P<0.01);大肠癌中p-MAPK与CyclinD1表达呈明显正相关(P<0.01),而与CDK4蛋白表达无明显相关性(P>0.05),CyclinD1和CDK4表达呈正相关(P<0.05),RT-PCR检测结果与免疫组化相似,p-MAPK、CyclinD1和CDK4蛋白的阳性表达率分别为8.2 %(61/78)、67.9 %(53/78)和53.8 %(42/78);相应癌旁组织中阳性表达率分别为3.8 %(3/78)、2.6 %(2/78)和6.4 %(5/78).结论 MAPK活化可能是cylinD1激活的原因之一,并在大肠癌发生过程中可能起重要作用;而Cyclin D1 在细胞周期中可与CDK4 结合,从而促进细胞周期进程.Objective To detect the expression of p-MAPK, CyclinD1 and CDK4 proteins in human colorectal carcinomas, and explore their correlations. Methods Seventy-eight samples of colorectal carcinoma tissues were intraoperatively obtained, and stained with HE for pathomorpho- logic examination, p-MAPK, CyclinD1 and CDK4 were detected in the 78 colorectal carcinoma, tumor adjacent colorectal carcinoma tissues and normal tissues by immunohistochemical method and RT-PCR. Results Positive expression rates for p-MAPK, CyelinD1 and CDK4 proteins in coloreetal carcinoma were 67.9 % (53/78) , 57.7 % (45/78) and 39.7 % (31/78) and in the tissues adjacent to tumors were 6.4 % (5/78), 10.3 % (8/78) and 19.2 % (15/78), respectively. Positive expression rates and levels of p-MAPK, CyclinD1 and CDK4 protein in carcinoma were significantly higher than those in the mucosa (P 〈 0.01 ) . Significant correlation between the expression of p-MAPK and CyclinD1 was found (P 〈0. 01 ) . There were no significant correlations between the expression of p-MAPK, CyelinD1 and CDK4 proteion (P 〉 0. 05) . The correlation between the expression of CyclinD1 and CDK4 was found (P 〈 0. 05) . The results of immunohisto- chemistry, RT-PCR indicated that positive expression rates for p-MAPK, CyclinD1 and CDK4 proteins in coloreetal carcinoma were 8.2 % (61/78) , 67.9 % (53/78) and 53.8 % (42/78) , and in the tissues adjacent to tumors were 3.8 % (3/78), 2.6 % (2/78) and 6.4 % (5/78). Conclusion The results indicate that MAPK may play an important role in the pathogenesis of colorectal carcinoma. The Cyclin D1 and cdk complex can promot cell cycle progression.
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