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通过全基因组表达荟萃分析鉴定GATA3作为乳腺癌预后标志物

Identification of GATA3 as a breast cancer prognostic marker by global gene expression meta-analysis.

作者信息

Mehra Rohit, Varambally Sooryanarayana, Ding Lei, Shen Ronglai, Sabel Michael S, Ghosh Debashis, Chinnaiyan Arul M, Kleer Celina G

机构信息

Department of Pathology, University of Michigan Medical School, Ann Arbor, 48109, USA.

出版信息

Cancer Res. 2005 Dec 15;65(24):11259-64. doi: 10.1158/0008-5472.CAN-05-2495.

Abstract

GATA binding protein 3 (GATA3) is a transcriptional activator highly expressed by the luminal epithelial cells in the breast. Here we did a meta-analysis of the available breast cancer cDNA data sets on a cohort of 305 patients and found that GATA3 was one of the top genes with low expression in invasive carcinomas with poor clinical outcome. To validate its prognostic utility, we did a tissue microarray analysis on a cohort of 139 consecutive invasive carcinomas (n = 417 tissue samples) immunostained with a monoclonal antibody against GATA3. Low GATA3 expression was associated with higher histologic grade (P < 0.001), positive nodes (P = 0.002), larger tumor size (P = 0.03), negative estrogen receptor and progesterone receptor (P < 0.001 for both), and HER2-neu overexpression (P = 0.03). Patients whose tumors expressed low GATA3 had significantly shorter overall and disease-free survival when compared with those whose tumors had high GATA3 levels. The hazard ratio of metastasis or recurrence according to the GATA3 status was 0.31 (95% confidence interval, 0.13-0.74; P = 0.009). Cox multivariate analysis showed that GATA3 had independent prognostic significance above and beyond conventional variables. Our data suggest that immunohistochemical analysis of GATA3 may be the basis for a new clinically applicable test to predict tumor recurrence early in the progression of breast cancer.

摘要

GATA结合蛋白3(GATA3)是一种转录激活因子,在乳腺腔上皮细胞中高度表达。我们对305例患者的乳腺癌cDNA数据集进行了荟萃分析,发现GATA3是侵袭性癌中低表达且临床预后较差的顶级基因之一。为了验证其预后价值,我们对139例连续侵袭性癌(n = 417个组织样本)进行了组织芯片分析,并用抗GATA3单克隆抗体进行免疫染色。GATA3低表达与更高的组织学分级(P < 0.001)、阳性淋巴结(P = 0.002)、更大的肿瘤大小(P = 0.03)、雌激素受体和孕激素受体阴性(两者P均 < 0.001)以及HER2-neu过表达(P = 0.03)相关。与肿瘤GATA3水平高的患者相比,肿瘤表达低GATA3的患者的总生存期和无病生存期明显更短。根据GATA3状态,转移或复发的风险比为0.31(95%置信区间,0.13 - 0.74;P = 0.009)。Cox多因素分析表明,GATA3除了传统变量外具有独立的预后意义。我们的数据表明,GATA3的免疫组化分析可能是一种新的临床适用检测方法的基础,用于在乳腺癌进展早期预测肿瘤复发。

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