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通过体内表达显性负性c-jun预防人乳头瘤病毒16型E7癌基因诱导的肿瘤发生

Protection against human papillomavirus type 16-E7 oncogene-induced tumorigenesis by in vivo expression of dominant-negative c-jun.

作者信息

Young Matthew R, Farrell Linda, Lambert Paul, Awasthi Parirokh, Colburn Nancy H

机构信息

Basic Research Laboratory, National Institute of Cancer-Frederick, Maryland, USA.

出版信息

Mol Carcinog. 2002 Jun;34(2):72-7. doi: 10.1002/mc.10050.

Abstract

Expression of the human papillomavirus (HPV) type 16 E6 and E7 gene products is a risk factor for human cervical carcinogenesis as well as skin and oral carcinogenesis. Expression of the HPV-16 E7 gene in mouse skin induces hyperplasia and enhances tumor promotion. Expression of dominant-negative c-jun (TAM67) in the mouse skin protects mice from 7,12-dimethylbenz[a]anthracene (DMBA)/12-O-tetradecanoylphorbol-13-acetate (TPA)-induced papillomagenesis without blocking mitogen-induced hyperproliferation. To determine the role of activator protein-1 (AP-1) in HPV-induced cancer, we crossed HPV-16 E7 mice with TAM67 mice and analyzed the effects of DMBA/TPA on tumor promotion. We showed that expression of TAM67 protected mice from HPV-16 E7-enhanced tumorigenesis, suggesting AP-1 as a target for prevention of HPV-induced cancer.

摘要

人乳头瘤病毒16型(HPV-16)E6和E7基因产物的表达是人类宫颈癌发生以及皮肤癌和口腔癌发生的危险因素。HPV-16 E7基因在小鼠皮肤中的表达会诱导增生并增强肿瘤促进作用。在小鼠皮肤中表达显性负性c-jun(TAM67)可保护小鼠免受7,12-二甲基苯并[a]蒽(DMBA)/12-O-十四烷酰佛波醇-13-乙酸酯(TPA)诱导的乳头状瘤发生,而不会阻断丝裂原诱导的过度增殖。为了确定活化蛋白-1(AP-1)在HPV诱导的癌症中的作用,我们将HPV-16 E7小鼠与TAM67小鼠杂交,并分析了DMBA/TPA对肿瘤促进的影响。我们发现TAM67的表达可保护小鼠免受HPV-16 E7增强的肿瘤发生,这表明AP-1是预防HPV诱导癌症的一个靶点。

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