Gupta R K, Norton A J, Thompson I W, Lister T A, Bodmer J G
ICRF Department of Medical Oncology, St Bartholomew's Hospital, West Smithfield, London, UK.
Br J Cancer. 1992 Oct;66(4):649-52. doi: 10.1038/bjc.1992.331.
Mutation of the p53 protein may represent the commonest genetic event in human malignancy. Abnormal p53 expression has been reported in a variety of carcinomas, sarcomas and lymphoid neoplasms; however there is little information in relation to Hodgkin's disease. The expression of the nuclear phosphoprotein was investigated in paraffin-embedded biopsies from fifty patients with Hodgkin's disease using a polyclonal antibody, CM-1 and in snap-frozen material with monoclonal antibodies, PAb 1801 and PAb 240. Specifically, immunoreactivity was localised to the Reed-Sternberg cells or mononuclear variants in both nodular sclerosing (86% cases) and mixed cellularity (57% cases) subtypes of Hodgkin's disease. However, no positive staining was found in our cases of nodular lymphocyte predominant type Hodgkin's disease. Serial biopsies following recurrence of disease demonstrated consistent results. It is suggested that overexpression of p53, probably mutant, may have a role in the tumorigenesis of Hodgkin's disease.
p53蛋白的突变可能是人类恶性肿瘤中最常见的基因事件。在多种癌、肉瘤和淋巴瘤中均有异常p53表达的报道;然而,关于霍奇金病的相关信息却很少。使用多克隆抗体CM-1对50例霍奇金病患者的石蜡包埋活检组织以及使用单克隆抗体PAb 1801和PAb 240对速冻材料进行研究,以检测核磷蛋白的表达。具体而言,在结节硬化型(86%的病例)和混合细胞型(57%的病例)霍奇金病亚型中,免疫反应性定位于里德-斯腾伯格细胞或单核变体。然而,在我们的结节性淋巴细胞为主型霍奇金病病例中未发现阳性染色。疾病复发后的系列活检显示结果一致。提示p53的过表达(可能是突变型)可能在霍奇金病的肿瘤发生中起作用。