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人乳头瘤病毒E6和E7癌蛋白与肿瘤抑制基因产物的相互作用。

Interactions of HPV E6 and E7 oncoproteins with tumour suppressor gene products.

作者信息

Münger K, Scheffner M, Huibregtse J M, Howley P M

机构信息

Laboratory of Tumour Virus Biology, National Cancer Institute, Bethesda, Maryland 20892.

出版信息

Cancer Surv. 1992;12:197-217.

PMID:1322242
Abstract

The HPVs associated with anogenital cancers encode two oncoproteins, E6 and E7. Both E6 and E7 can form specific complexes with tumour suppressor gene products. The E7 protein binds to the retinoblastoma tumour suppressor gene product pRB, with a preference for the underphosphorylated, "active" form of pRB. The E7 proteins derived from the "high risk" HPVs bind to pRB with a higher affinity than the E7 proteins from the "low risk" HPVs. The "high risk" HPV E6 proteins can associate with the p53 tumour suppressor protein. This interaction promotes the degradation of p53 in vitro, which presumably accounts for the very low levels of p53 in cervical carcinoma cell lines. The functional inactivation of pRB and p53 by the HPV oncoproteins E7 and E6, respectively, are likely to be important steps in cervical carcinogenesis, since mutations in the RB and p53 genes were detected in HPV negative but not HPV positive cervical carcinoma cell lines. Cytogenetic studies strongly suggest, however, that additional chromosomal changes may be necessary for carcinogenic progression of HPV induced anogenital lesions.

摘要

与肛门生殖器癌相关的人乳头瘤病毒(HPV)编码两种癌蛋白,即E6和E7。E6和E7都能与肿瘤抑制基因产物形成特定复合物。E7蛋白与视网膜母细胞瘤肿瘤抑制基因产物pRB结合,更倾向于未磷酸化的“活性”形式的pRB。源自“高危”HPV的E7蛋白比源自“低危”HPV的E7蛋白与pRB的结合亲和力更高。“高危”HPV E6蛋白可与p53肿瘤抑制蛋白结合。这种相互作用在体外促进p53的降解,这大概可以解释子宫颈癌细胞系中p53水平极低的原因。HPV癌蛋白E7和E6分别导致pRB和p53的功能失活,这可能是子宫颈癌发生过程中的重要步骤,因为在HPV阴性而非HPV阳性的子宫颈癌细胞系中检测到RB和p53基因的突变。然而,细胞遗传学研究强烈表明,HPV诱导的肛门生殖器病变的致癌进展可能还需要其他染色体变化。

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