Expression of the cell cycle regulatory proteins p34cdc2, p21waf1, and p53 in node negative invasive ductal breast carcinoma.

H P Kourea, A K Koutras, C D Scopa, M N Marangos, E Tzoracoeleftherakis, D Koukouras, H P Kalofonos
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引用次数: 27

Abstract

Aims: To look for correlations between expression of cell cycle regulatory proteins p34(cdc2), p21(WAF1), and p53 in node negative invasive ductal breast carcinoma, or between these proteins and clinicopathological parameters, and to assess their prognostic value.

Methods: Immunohistochemistry using formalin fixed, paraffin wax embedded sections from 94 breast carcinomas. Adjacent benign epithelial breast tissue was available in 74 cases. Median follow up was 72 months.

Results: Nuclear and cytoplasmic p34(cdc2) expression was seen in 80 and 62 tumours, respectively; nuclear expression was seen in adjacent benign epithelium in 12 cases. p21(WAF1) and p53 were positive in 48 and 21 tumours, respectively. High expression of p34(cdc2) in neoplastic nuclei was associated with higher histological grade and p53 expression, but not with tumour size, steroid receptor status, patient age, menopausal status, recurrence, metastasis, disease free survival (DFS), or overall survival (OS). p34(cdc2) in tumour cytoplasm was associated with p34(cdc2) nuclear positivity, high tumour grade, and DFS in univariate but not multivariate analysis. In contrast, p34(cdc2) expression in benign tissue independently predicted DFS and OS in univariate and multivariate analysis. Expression of p53 was associated with high tumour grade and negative steroid receptors, but not with recurrence, metastasis, DFS, or OS. p21(WAF1) expression was not associated with the examined parameters.

Conclusions: p34(cdc2), p21(WAF1), and p53 expression does not predict outcome in node negative breast carcinoma, although p34(cdc2) expression in benign tissue is related to prognosis. The association between p34(cdc2) and p53 implicates p53 in G2-M cell cycle checkpoint control, possibly via mediators unrelated to p21(WAF1).

细胞周期调节蛋白p34cdc2、p21waf1和p53在淋巴结阴性浸润性导管性乳腺癌中的表达
目的:探讨细胞周期调节蛋白p34(cdc2)、p21(WAF1)、p53在淋巴结阴性浸润性导管乳腺癌中的表达及其与临床病理参数的相关性,并评价其预后价值。方法:采用免疫组化法,采用福尔马林固定、石蜡包埋法对94例乳腺癌切片进行免疫组化处理。74例乳腺旁有良性上皮组织。中位随访时间为72个月。结果:细胞核表达p34(cdc2) 80例,细胞质表达cdc2 62例;12例癌旁良性上皮可见核表达。p21(WAF1)和p53分别在48例和21例肿瘤中呈阳性。肿瘤细胞核中p34(cdc2)的高表达与较高的组织学分级和p53表达相关,但与肿瘤大小、类固醇受体状态、患者年龄、绝经状态、复发、转移、无病生存期(DFS)或总生存期(OS)无关。在单因素分析中,肿瘤细胞质中p34(cdc2)与p34(cdc2)核阳性、高肿瘤分级和DFS相关,而非多因素分析。相比之下,p34(cdc2)在良性组织中的表达在单因素和多因素分析中独立预测DFS和OS。p53的表达与高肿瘤分级和阴性类固醇受体相关,但与复发、转移、DFS或OS无关。p21(WAF1)表达与检测参数无关。结论:p34(cdc2)、p21(WAF1)和p53的表达不能预测淋巴结阴性乳腺癌的预后,尽管良性组织中p34(cdc2)的表达与预后有关。p34(cdc2)和p53之间的关联暗示p53可能通过与p21无关的介质(WAF1)参与G2-M细胞周期检查点控制。
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