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作 者:李培峰[1] 刘晓红[1] 曹永成[1] 王翠翠[1] 周露婷[1] 耿明[1]
出 处:《中国医师杂志》2014年第5期588-591,共4页Journal of Chinese Physician
基 金:国家自然科学基金(81172261)
摘 要:目的 检测Wnt-5a基因和基因产物在原发性肝细胞癌中的表达,探讨Wnt-5a基因在肝癌发生过程中的作用和临床意义.方法 采用实时定量PCR技术,检测Wnt-5a mRNA在26例新鲜肝细胞癌和癌旁组织中的含量;用免疫组化法观察Wnt-5a蛋白在85例肝细胞癌和癌旁组织、15例肝硬化组织中的表达.结果 Wnt-5a mRNA在肝癌及癌旁组织中的相对含量分别为0.102 127±0.158 620和0.020 106±0.022 075,两者间差异有统计学意义(P<0.05);Wnt-5a蛋白在肝细胞癌、癌旁组织和肝硬化中的阳性率分别为21.2% (18/85)、81.26% (69/85)和86.7% (13/15),Wnt-5a在肝癌组织中的阳性表达显著低于肝硬化和癌旁组织,差异有统计学意义(P <0.01);Wnt-5a蛋白在肝癌中的表达与肿瘤的TNM分期和血清甲胎蛋白(AFP)含量有关(P<0.05).结论 Wnt-5a基因在HCC基因转录中呈上调表达,而在蛋白水平显示为缺失和下调表达,提示肿瘤细胞是在蛋白翻译水平而不是转录水平干扰了Wnt-5a基因功能.Objective To investigate the expression of Wnt-5a gene in primary hepatocellular carcinoma (HCC) and to expose its role and clinical significance in the development of HCC.Methods Real time quantitative reverse transcription polymerase chain reaction (RT-PCR) was performed in 26 fresh HCC samples and the corresponding para-carcinoma tissues to detect mRNA expression of Wnt-5a gene.Wnt-5a protein was detected with immunohistochemical method in paraffin embedding tissues of 85 cases of HCCs and the corresponding para-carcinoma tissues,and 15 cases of hepatic cirrhosis.Results RT-PCR analysis showed that Wnt-5a mRNA (0.102 127 ±0.158 620) in the HCC tissues was more than that (0.020 106 ±0.022 075) in the para-carcinoma tissues (P〈0.05).The positive expression rate of Wnt-5a protein in HCC,para-carcinoma,and hepatic cirrhosis tissues were 21.2% (18/85),81.26% (69/85),and 86.7% (13/15),respectively.The positive rate of Wnt-5a was significantly lower in the HCC than in the para-carcinoma and hepatic cirrhosis tissues (P 〈 0.01).The expression of Wnt-5a was significantly associated with lower tumor node metastasis (TNM) stages and small alpha fetoproteins (AFP) content of blood serum (P 〈0.05).Conclusions The high expression of Wnt-5a mRNA was found in the gene transcription of HCC,while Wnt-5a protein was absent or low in HCC.It was suggested that the roles of Wnt-5a was interfered at the protein level rather than the transcriptional level in the HCC.
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