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人乳头瘤病毒16/18型转化(E6)癌蛋白与p53肿瘤抑制基因蛋白在食管癌中的免疫组织化学共表达

Immunohistochemical co-expression of human papillomavirus type 16/18 transforming (E6) oncoprotein and p53 tumour suppressor gene proteins in oesophageal cancer.

作者信息

Agarwal S K, Chatterji A, Bhambhani S, Sharma B K

机构信息

Department of Medicine, Maulana Azad Medical College, New Delhi, India.

出版信息

Indian J Exp Biol. 1998 Jun;36(6):559-63.

PMID:9731468
Abstract

Human papillomaviruses have been widely implicated as important etiologic agents in various squamous cell carcinomas including oesophageal carcinoma. p53 mutant oncoprotein has also been implicated in various tumours. Immunohistochemical analysis was employed to detect the co-expression of HPV and p53 mutant protein in biopsy specimens of patients of cancer oesophagus as well as controls. This analysis revealed a significantly higher immunopositivity (63%) of E6 oncoprotein of HPV 16/18 in carcinoma of the oesophagus. Immunoexpression of E6 oncoprotein of HPV did not alter significantly the degree of differentiation of the tumour. Seventy-seven percent of cases of oesophageal carcinoma showed strong immuno-staining for mutant p53 protein. A higher percentage (89%) of tissues showed immunoexpression of mutant p53 protein in conjunction with E6 oncoprotein of HPV 16/18 indicating a selective degradation of key cellular protein of p53 having regulatory properties which in turn leads to uncontrolled cellular proliferation. Therefore, coexpression of oncoprotein E6 of HPV 16/18 and mutant p53 protein may be considered as a "high risk" factor for progression to oesophageal malignancy.

摘要

人乳头瘤病毒已被广泛认为是包括食管癌在内的各种鳞状细胞癌的重要病因。p53突变癌蛋白也与各种肿瘤有关。采用免疫组织化学分析来检测食管癌患者活检标本以及对照中HPV和p53突变蛋白的共表达情况。该分析显示,在食管癌中HPV 16/18的E6癌蛋白免疫阳性率显著更高(63%)。HPV的E6癌蛋白免疫表达并未显著改变肿瘤的分化程度。77%的食管癌病例对突变p53蛋白呈强免疫染色。更高比例(89%)的组织显示突变p53蛋白与HPV 16/18的E6癌蛋白共同免疫表达,表明具有调节特性的关键细胞蛋白p53被选择性降解,进而导致细胞增殖失控。因此,HPV 16/18的癌蛋白E6与突变p53蛋白的共表达可被视为进展为食管恶性肿瘤的“高危”因素。

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引用本文的文献

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The aetiological role of human papillomavirus in oesophageal squamous cell carcinoma: a meta-analysis.
PLoS One. 2013 Jul 24;8(7):e69238. doi: 10.1371/journal.pone.0069238. Print 2013.

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