口腔癌及癌旁正常黏膜中p53表达与多发原发癌发生的关系

V. Bongers , G.B. Snow , I. van der Waal , B.J.M. Braakhuis
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引用次数: 37

摘要

使用Bp53-11抗体对原发口腔鳞状细胞癌患者的石蜡包埋、福尔马林固定组织切片进行免疫组织化学检测,检测p53的表达。本研究的目的是确定p53表达作为呼吸和上消化道第二原发性肿瘤(SPT)发展的生物标志物的预测价值。在一项巢式病例对照研究中,使用了44名既往有癌症病史的患者的肿瘤和正常组织切片。44例中有15例发展为SPT,而其他29例至少7年无疾病。此外,本研究还纳入了9个spt,以确定在同一领域发展的肿瘤中是否存在一致性。随访期间无肿瘤的29例患者中有10例(34%)为p53阳性肿瘤。15例发生SPT的患者中有8例(53%)原发肿瘤为p53阳性。该差异无统计学差异(χ2-test)。40%的原发性口腔肿瘤呈p53阳性。当比较第一和第二肿瘤时,9例中有4例在第一和第二肿瘤中发现p53表达不一致。邻近正常黏膜无p53阳性。总之,肿瘤、非典型增生和正常组织中p53的免疫反应性不能预测SPT的发展。此外,多个原发肿瘤的p53表达并不相同。
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value of p53 expression in oral cancer and adjacent normal mucosa in relation to the occurrence of multiple primary carcinomas

Paraffin embedded, formalin fixed tissue sections from patients suffering from a primary oral squamous cell carcinoma were immunohistochemically investigated for the presence of p53 expression using the Bp53-11 antibody. The aim of this study was to determine the predictive value of p53 expression as a biomarker for the development of a second primary tumour (SPT) in the respiratory and upper digestive tract. In a nested case control study, neoplastic and normal tissue sections of 44 patients who had a previous history of cancer were used. 15 of the 44 had developed a SPT, while the other 29 were minimally 7 years free of disease. Additionally, nine SPTs were included in this study to establish whether concordance exists in tumours that develop in the same field. 10 of the 29 patients (34%) free of tumour during follow-up had p53 positive tumours. 8 of 15 patients (53%) who developed a SPT had a p53 positive primary tumour. This difference is not statistically different (χ2-test). Forty per cent of the total group of primary oral cavity tumours showed p53 positivity. When comparing the first and the second tumours, discordance in p53 expression between the first and second tumours was seen in 4 out of 9 cases. None of the cases showed p53 positivity in adjacent normal mucosa. In conclusion, p53 immunoreactivity in neoplasia, dysplasia and normal tissue does not predict the development of a SPT. In addition, multiple primary tumours do not have identical p53 expression.

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