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非裔美国女性的 AR 阴性三阴性或“四重阴性”乳腺癌具有丰富的基底和免疫特征。

AR negative triple negative or "quadruple negative" breast cancers in African American women have an enriched basal and immune signature.

机构信息

Department of Public Health Sciences, Henry Ford Health Systems and Henry Ford Cancer Institute, Detroit, MI, United States of America.

Department of Biology & Center for Cancer Research, Tuskegee University, Tuskegee, AL, United States of America.

出版信息

PLoS One. 2018 Jun 18;13(6):e0196909. doi: 10.1371/journal.pone.0196909. eCollection 2018.

DOI:10.1371/journal.pone.0196909
PMID:29912871
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6005569/
Abstract

There is increasing evidence that Androgen Receptor (AR) expression has prognostic usefulness in Triple negative breast cancer (TNBC), where tumors that lack AR expression are considered "Quadruple negative" Breast Cancers ("QNBC"). However, a comprehensive analysis of AR expression within all breast cancer subtypes or stratified by race has not been reported. We assessed AR mRNA expression in 925 tumors from The Cancer Genome Atlas (TCGA), and 136 tumors in 2 confirmation sets. AR protein expression was determined by immunohistochemistry in 197 tumors from a multi-institutional cohort, for a total of 1258 patients analyzed. Cox hazard ratios were used to determine correlations to PAM50 breast cancer subtypes, and TNBC subtypes. Overall, AR-negative patients are diagnosed at a younger age compared to AR-positive patients, with the average age of AA AR-negative patients being, 49. AA breast tumors express AR at lower rates compared to Whites, independent of ER and PR expression (p<0.0001). AR-negative patients have a (66.60; 95% CI, 32-146) odds ratio of being basal-like compared to other PAM50 subtypes, and this is associated with an increased time to progression and decreased overall survival. AA "QNBC" patients predominately demonstrated BL1, BL2 and IM subtypes, with differential expression of E2F1, NFKBIL2, CCL2, TGFB3, CEBPB, PDK1, IL12RB2, IL2RA, and SOS1 genes compared to white patients. Immune checkpoint inhibitors PD-1, PD-L1, and CTLA-4 were significantly upregulated in both overall "QNBC" and AA "QNBC" patients as well. Thus, AR could be used as a prognostic marker for breast cancer, particularly in AA "QNBC" patients.

摘要

越来越多的证据表明,雄激素受体 (AR) 的表达在三阴性乳腺癌 (TNBC) 中具有预后作用,缺乏 AR 表达的肿瘤被认为是“四重阴性”乳腺癌 (“QNBC”)。然而,尚未有关于 AR 表达在所有乳腺癌亚型中的综合分析或按种族分层的报告。我们评估了来自癌症基因组图谱 (TCGA) 的 925 个肿瘤和 2 个确认集的 136 个肿瘤中的 AR mRNA 表达。在一个多机构队列的 197 个肿瘤中通过免疫组织化学测定 AR 蛋白表达,共分析了 1258 例患者。Cox 风险比用于确定与 PAM50 乳腺癌亚型和 TNBC 亚型的相关性。总体而言,与 AR 阳性患者相比,AR 阴性患者的诊断年龄较小,AA AR 阴性患者的平均年龄为 49 岁。AA 乳腺肿瘤的 AR 表达率低于白人,与 ER 和 PR 表达无关 (p<0.0001)。与其他 PAM50 亚型相比,AR 阴性患者的基底样 (basal-like) 比值比为 (66.60; 95%CI, 32-146),这与进展时间延长和总生存期缩短相关。AA“QNBC”患者主要表现为 BL1、BL2 和 IM 亚型,与白人患者相比,E2F1、NFKBIL2、CCL2、TGFB3、CEBPB、PDK1、IL12RB2、IL2RA 和 SOS1 基因的表达存在差异。免疫检查点抑制剂 PD-1、PD-L1 和 CTLA-4 在总“QNBC”和 AA“QNBC”患者中均显著上调。因此,AR 可作为乳腺癌的预后标志物,特别是在 AA“QNBC”患者中。

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FOXM1 Transcriptionally Co-Upregulates Centrosome Amplification and Clustering Genes and Is a Biomarker for Poor Prognosis in Androgen Receptor-Low Triple-Negative Breast Cancer.FOXM1转录共上调中心体扩增和聚集相关基因,是雄激素受体低表达三阴性乳腺癌预后不良的生物标志物。
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