Fouret P, Dabit D, Sibony M, Alili D, Commo F, Saint-Guily J L, Callard P
Anatomy Pathology Service, Tenon Hospital, Paris, France.
Am J Pathol. 1995 Mar;146(3):599-604.
The aim of this study was to gain some insight into the relationship of human papillomavirus (HPV) infection to p53 expression and to some pathological parameters in precancerous lesions of the larynx. Formalin-fixed paraffin-embedded tissue sections containing human laryngeal precancerous lesions were screened for p53 protein by immunohistochemistry with the monoclonal antibody DO7 and for the presence of HPV infection by polymerase chain reaction with consensus primers directed against the E6 gene. The presence of p53 protein was detected in 31 of 57 specimens (54.4%) including 7 of 9 cases with mild dysplasia (78%), in 4 of 9 cases with moderate dysplasia (44%), and in 15 of 23 cases with severe dysplasia (65%). Of 16 samples with keratotic benign squamous metaplasia, 5 were also p53 positive (31%). Of 6 samples that were HPV positive, all were of type 16. Interestingly, 3 of the 6 HPV-positive samples were p53 negative. There was 1 HPV-positive case with strong p53 staining and 2 HPV-positive cases with minimal p53 staining. The 2 HPV-positive cases with minimal p53 staining had mild dysplasia. The HPV-positive case with strong p53 staining displayed severe dysplasia. Of 23 cases that were both HPV and p53 negative, 11 presented with keratosis and no dysplasia, 5 with moderate dysplasia, and 7 with severe dysplasia. Our data indicate that nuclear accumulation of p53 protein, presumably resulting from p53 gene mutation, may occur in HPV-infected epithelial tissues. On the other hand, there are many precancer lesions, some exhibiting moderate or severe dysplasia, that are both HPV negative and p53 unreactive, suggesting that alterations of genes other than the E6 oncogene and the p53 tumor suppressor gene play a role in early laryngeal carcinogenesis.
本研究旨在深入了解人乳头瘤病毒(HPV)感染与喉癌前病变中p53表达及某些病理参数之间的关系。采用单克隆抗体DO7通过免疫组织化学法对含有人喉癌前病变的福尔马林固定石蜡包埋组织切片进行p53蛋白筛查,并采用针对E6基因的共有引物通过聚合酶链反应检测HPV感染情况。在57个标本中的31个(54.4%)检测到p53蛋白,其中9例轻度发育异常中有7例(78%),9例中度发育异常中有4例(44%),23例重度发育异常中有15例(65%)。在16例角化性良性鳞状化生样本中,5例p53也呈阳性(31%)。在6例HPV阳性样本中,均为16型。有趣的是,6例HPV阳性样本中有3例p53呈阴性。有1例HPV阳性病例p53染色强,2例HPV阳性病例p53染色弱。2例p53染色弱的HPV阳性病例为轻度发育异常。p53染色强的HPV阳性病例显示为重度发育异常。在23例HPV和p53均为阴性的病例中,11例表现为角化,无发育异常,5例为中度发育异常,7例为重度发育异常。我们的数据表明,p53蛋白的核内积聚可能是由p53基因突变引起的,可能发生在HPV感染的上皮组织中。另一方面,有许多癌前病变,有些表现为中度或重度发育异常,HPV和p53均无反应,这表明除E6癌基因和p53肿瘤抑制基因外的其他基因改变在喉癌早期发生中起作用。