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CCAAT/增强子结合蛋白C/EBPα、C/EBPβ和C/EBPδ在乳腺癌中的表达:与临床病理参数及细胞周期调节蛋白的相关性

Expression of the CCAAT/enhancer-binding proteins C/EBPalpha, C/EBPbeta and C/EBPdelta in breast cancer: correlations with clinicopathologic parameters and cell-cycle regulatory proteins.

作者信息

Milde-Langosch Karin, Löning Thomas, Bamberger Ana-Maria

机构信息

Institute of Pathology, Department of Gynecopathology, University-Hospital Hamburg-Eppendorf (UKE), Hamburg, Germany.

出版信息

Breast Cancer Res Treat. 2003 May;79(2):175-85. doi: 10.1023/a:1023929504884.

Abstract

Members of the CCAAT/enhancer-binding protein (C/EBP) family of transcription factors are involved in the regulation of proliferation and differentiation of the mammary gland. In order to investigate the role of C/EBPalpha, -beta and -delta in breast cancer, we performed western blot analysis and partly immunohistochemistry in 75 mammary carcinomas, 10 normal mammary tissue samples and four mammary cell lines. Expression levels of both C/EBPalpha isoforms, C/EBPbeta isoforms LAP1, LAP2 (liver-enriched transcriptional activating proteins), and LIP (liver-enriched transcriptional inhibitory protein), and C/EBPdelta in the tumors were correlated with clinicopathological tumor parameters, expression of estrogen and progesterone receptors (ER, PR), Ki67 immunostaining, and expression of seven cell-cycle regulatory proteins which had been analyzed before. High C/EBPalpha and -delta protein levels correlated significantly with expression of cell-cycle promoters (cyclin D1 and E) and cell-cycle inhibitory proteins (Rb, p27, p16), but with none of the established prognostic parameters. In contrast, statistically significant relationships of the full-length C/EBPbeta isoform LAP1 and a negative estrogen receptor status, high grading, nodal involvement, and high cyclin E and p16 expression were found. For the shorter isoform LIP, correlations with an ER-negative phenotype and high Ki67 immunostaining were detected, and high histological grading (G3) correlated with lower LAP/LIP ratio. These results suggest that high C/EBPbeta expression might be involved in tumor progression and indicative of an unfavorable prognosis.

摘要

CCAAT/增强子结合蛋白(C/EBP)转录因子家族成员参与乳腺的增殖和分化调控。为了研究C/EBPα、-β和-δ在乳腺癌中的作用,我们对75例乳腺癌、10例正常乳腺组织样本和4种乳腺细胞系进行了蛋白质免疫印迹分析,并部分进行了免疫组织化学分析。肿瘤中C/EBPα两种异构体、C/EBPβ异构体LAP1、LAP2(肝脏富集转录激活蛋白)、LIP(肝脏富集转录抑制蛋白)以及C/EBPδ的表达水平与临床病理肿瘤参数、雌激素和孕激素受体(ER、PR)表达、Ki67免疫染色以及之前分析的7种细胞周期调节蛋白的表达相关。高C/EBPα和-δ蛋白水平与细胞周期启动子(细胞周期蛋白D1和E)和细胞周期抑制蛋白(Rb、p27、p16)的表达显著相关,但与任何已确立的预后参数均无关联。相比之下,发现全长C/EBPβ异构体LAP1与雌激素受体阴性状态、高分级、淋巴结受累以及高细胞周期蛋白E和p16表达之间存在统计学显著关系。对于较短的异构体LIP,检测到其与ER阴性表型和高Ki67免疫染色相关,高组织学分级(G3)与较低的LAP/LIP比值相关。这些结果表明,高C/EBPβ表达可能参与肿瘤进展并提示预后不良。

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