Horne G M, Anderson J J, Tiniakos D G, McIntosh G G, Thomas M D, Angus B, Henry J A, Lennard T W, Horne C H
Department of Pathology, Royal Victoria Infirmary, University of Newcastle upon Tyne, UK.
Br J Cancer. 1996 Jan;73(1):29-35. doi: 10.1038/bjc.1996.6.
We examined the reactivity of four p53-specific monoclonal antibodies--PAb 1801, p53-BP-12, D07 and CM1--on sections of formalin-fixed tissue collected from 245 breast carcinomas. Immunodetection of p53 varied between 37.6% and 46.6%. The greatest variation was observed among lobular carcinomas and low-grade tumors in which immunodetection varied between 8.3% and 27.3%. In contrast, immunodetection of p53 in invasive ductal carcinomas was subject to a lower degree of variability with between 40.6% and 49.7% of these tumours proving to be positive. In general, we found antibodies PAb 1801 and DO7 to be the most effective in immunolocalising p53. Immunodetection of p53 with each of the four antibodies was found to correlate strongly with tumour grade. In survival analysis, the results gained using antibody PAb 1801 proved to be of greatest statistical significance and to provide the strongest index of prognosis. A significant relationship was observed between immunodetection of p53 with each of the four antibodies and poor responsiveness to endocrine therapy. In addition, relationships were also observed between p53 immunostaining and tumour oestrogen receptor (ER) status as well as c-jun expression. We observed no correlation between abnormalities of the p53 and the Rb gene products or between elevated c-erbB-2 or epidermal growth factor receptor (EGFR) expression and immunodetection of p53.
我们检测了四种p53特异性单克隆抗体——PAb 1801、p53-BP-12、D07和CM1——对245例乳腺癌福尔马林固定组织切片的反应性。p53的免疫检测率在37.6%至46.6%之间。小叶癌和低级别肿瘤中的变化最大,其免疫检测率在8.3%至27.3%之间。相比之下,浸润性导管癌中p53的免疫检测率变异性较低,其中40.6%至49.7%的肿瘤呈阳性。总体而言,我们发现抗体PAb 1801和D07在免疫定位p53方面最有效。发现用这四种抗体中的每一种进行p53的免疫检测都与肿瘤分级密切相关。在生存分析中,使用抗体PAb 1801获得的结果被证明具有最大的统计学意义,并提供了最强的预后指标。观察到用这四种抗体中的每一种进行p53的免疫检测与内分泌治疗反应不佳之间存在显著关系。此外,还观察到p53免疫染色与肿瘤雌激素受体(ER)状态以及c-jun表达之间的关系。我们未观察到p53与Rb基因产物异常之间或c-erbB-2或表皮生长因子受体(EGFR)表达升高与p53免疫检测之间的相关性。