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原发性肝细胞性肝癌中p16基因的失活与P16蛋白表达的研究
引用本文:黄建钊,沈文律.原发性肝细胞性肝癌中p16基因的失活与P16蛋白表达的研究[J].华西医科大学学报,2000,31(3):306-309.
作者姓名:黄建钊  沈文律
作者单位:[1]同济医科大学同济医院器官移植研究所,武汉 [2]华西医科大学附属第一医院普外科,武汉
摘    要:为探讨p16基因与原发性肝细胞性肝癌(HCC)的关系,作者分别采用多重PCR、SSCP以及以PCR为基础的甲基化分析法,对25例原发性HCC标本及其相应的非肿瘤肝组织标本中p16基因的缺失,点突变及甲基化情况进行了检测。另用免疫组化SLAB法对35例(包括前述已作基因检测的25例)原发性HCC肿瘤标本及其相应的非肿瘤组织标本中P16蛋白的表达情况进行了检测。结果:25例原发性HCC肿瘤标本中,3例

关 键 词:p16基因  肝细胞癌  免疫组织化学  P16蛋白

A study on the inactivation of p16 genes and the expression of P16 protein in primary hepatocellular carcinomas]
J Huang,W Shen,B Li,Y Luo,S Liao,W Zhang,N Cheng.A study on the inactivation of p16 genes and the expression of P16 protein in primary hepatocellular carcinomas][J].Journal of West China University of Medical Sciences,2000,31(3):306-309.
Authors:J Huang  W Shen  B Li  Y Luo  S Liao  W Zhang  N Cheng
Institution:Organ Transplantation Research Institute, Tongji Hospital, Tongji University of Medical Sciences, Wuhan 430030.
Abstract:The aim of the present study was to determine whether p16 gene is involved in the genesis of primary hepatocellular carcinoma (HCC). Twenty-five primary HCC tumor and corresponding non-tumor liver tissue specimens were examined for P16 gene alterations. The identification of deletion of p16 gene exon 1 and exon 2 was performed using comparative multiplex polymerase chain reaction (PCR) analysis. The point mutation of p16 gene exon 2 was investigated by single strand conformational polymorphism(SSCP) analysis, and the status of p16 gene methylation was screened using PCR-based methylation analysis. Moreover, 35 parafin specimens of primary HCCs with corresponding non-tumor liver tissues, including the 25 cases described above for screening of p16 gene alterations, were investigated also for P16 protein expression by using immunohistochemical analysis. The results of comparative multiplex PCR analysis showed that 12% (3/25) p16 gene deletions, including homozygous deletions in 2 tumors and hemizygous deletion in 1 tumor, were found in the primary HCCs samples. No point mutation was identified in the remaining 22 tumor samples without p16 gene deletions by using SSCP analysis. Hypermethylation was detected in 24% (6/25) of tumor samples by PCR-based analysis. However the corresponding non-tumor liver tissue specimens were always unmethylated at p16 locus. Loss of P16 protein expression, detected by immunohistochemistry, occurred in 16 of 35 (45.7%) tumor samples, whereas all the non-tumor liver tissue specimens showed positive p16 staining. These results indicate that inactivation of p16 gene is relevant to the genesis of HCC.
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