Walker C, Robertson L J, Myskow M W, Pendleton N, Dixon G R
Clatterbridge Cancer Research Trust, J K Douglas Cancer Research Laboratory, Clatterbridge Hospital, Bebington, Wirral, UK.
Br J Cancer. 1994 Aug;70(2):297-303. doi: 10.1038/bjc.1994.296.
Bronchial epithelial dysplasia is thought to be a premalignant stage in the evolution of lung cancers. Using the CM-1 polyclonal antibody, we have examined the expression of the p53 protein in a larger series of bronchial dysplasias (n = 60) than hitherto investigated. The p53 protein was detected in 14% of mild, 25% of moderate and 59% of severe dysplasias; increased p53 expression correlated with the severity of dysplasia. p53-positive dysplasias had greater PCNA indices than p53-negative dysplasias. p53 expression in dysplastic tissues was compared with that in two groups of histologically normal epithelium: 14 bronchial biopsies from non-cancer patients of which all but one were negative and 32 bronchial margins from resected carcinomas, of which 17 showed infrequent solitary cells with p53-positive nuclei in predominantly basal locations scattered throughout the epithelium. These results for resection margins were confirmed by use of a second antibody, DO-1. Sixty-nine per cent of the corresponding carcinomas were p53 positive, but in 15 cases the p53 reactivity differed from resection margins. No correlation between p53 expression and any of the clinicopathological characteristics of these tumours was found. This study supports the observation that abnormal p53 expression may be an early but not obligatory event in malignant transformation in lung.
支气管上皮发育异常被认为是肺癌演变过程中的一个癌前阶段。我们使用CM - 1多克隆抗体,对一系列数量比以往研究更多的支气管发育异常(n = 60)样本检测了p53蛋白的表达情况。在轻度发育异常样本中,14%检测到p53蛋白;中度发育异常样本中,25%检测到;重度发育异常样本中,59%检测到。p53表达增加与发育异常的严重程度相关。p53阳性的发育异常样本的增殖细胞核抗原(PCNA)指数高于p53阴性的样本。将发育异常组织中的p53表达情况与两组组织学正常的上皮组织进行比较:一组是取自非癌症患者的14份支气管活检样本,除一份外其余均为阴性;另一组是取自切除癌组织的32份支气管切缘样本,其中17份显示在整个上皮组织中主要位于基底部位有散在的罕见单个p53阳性核细胞。使用第二种抗体DO - 1证实了这些切缘样本的结果。相应癌组织中有69%为p53阳性,但在15例中,p53反应性与切缘不同。未发现p53表达与这些肿瘤的任何临床病理特征之间存在相关性。本研究支持以下观点:p53表达异常可能是肺部恶性转化过程中的一个早期但并非必然出现的事件。