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mdm2基因的表达可能与人肝细胞癌中p53基因的畸变有关。

The expression of the mdm2 gene may be related to the aberration of the p53 gene in human hepatocellular carcinoma.

作者信息

Qiu S J, Ye S L, Wu Z Q, Tang Z Y, Liu Y K

机构信息

Liver Cancer Institute, Shanghai Medical University, PR China.

出版信息

J Cancer Res Clin Oncol. 1998;124(5):253-8. doi: 10.1007/s004320050162.

DOI:10.1007/s004320050162
PMID:9645455
Abstract

The relationship between mdm2 gene expression and p53 gene mutation in hepatocellular carcinoma (HCC) and their correlation with the invasiveness of the disease were investigated in this study. Either the expression level of the mdm2 gene or the mutation rate of the p53 gene was higher in HCC than in paratumor liver tissues. Studies on the relationship between mdm2 and p53 revealed that mdm2 gene expression in HCC without p53 mutation was higher than when there was p53 mutation, while the p53 mutation rate in HCC with mdm2 overexpression was significantly lower than in HCC without mdm2 overexpression. Among 23 HCC with invasion, mdm2 gene overexpression was found in 6 patients while p53 mutation was found in the other 11 patients, and only 1 patient was found to have both mdm2 overexpression and p53 mutation. These results indicated that either mdm2 overexpression or p53 mutation may be related to the invasiveness of HCC. Considering that an autoregulatory feedback loop between the mdm2 and p53 genes may exist, wild-type P53 can induce the expression of mdm2 via a p53-binding site in the mdm2 gene, while MDM2 protein functions as a negative regulator of P53 protein. These results also suggest that mdm2 may be related to the high invasiveness of HCC through inactivating the tumor-suppressor function of the p53 gene.

摘要

本研究调查了肝细胞癌(HCC)中mdm2基因表达与p53基因突变之间的关系及其与疾病侵袭性的相关性。HCC中mdm2基因的表达水平或p53基因的突变率均高于癌旁肝组织。对mdm2与p53关系的研究表明,无p53突变的HCC中mdm2基因表达高于有p53突变时,而mdm2过表达的HCC中p53突变率显著低于无mdm2过表达的HCC。在23例有侵袭的HCC中,6例患者存在mdm2基因过表达,11例患者存在p53突变,仅1例患者同时存在mdm2过表达和p53突变。这些结果表明,mdm2过表达或p53突变可能与HCC的侵袭性有关。鉴于mdm2与p53基因之间可能存在自动调节反馈环,野生型P53可通过mdm2基因中的p53结合位点诱导mdm2表达,而MDM2蛋白作为P53蛋白的负调节因子。这些结果还表明,mdm2可能通过使p53基因的肿瘤抑制功能失活而与HCC的高侵袭性有关。

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