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MHC II 途径在三阴性乳腺癌肿瘤细胞中的表达与良好的预后和浸润淋巴细胞相关。

Expression of the MHC Class II Pathway in Triple-Negative Breast Cancer Tumor Cells Is Associated with a Good Prognosis and Infiltrating Lymphocytes.

机构信息

Department of Medicine, University of Alabama at Birmingham, Comprehensive Cancer Center, Birmingham, Alabama.

Department of Pathology, University of Alabama at Birmingham, Comprehensive Cancer Center, Birmingham, Alabama.

出版信息

Cancer Immunol Res. 2016 May;4(5):390-9. doi: 10.1158/2326-6066.CIR-15-0243. Epub 2016 Mar 15.

Abstract

Triple-negative breast cancer (TNBC) is a subtype with heterogeneous patient outcomes. Approximately 40% of patients experience rapid relapse, while the remaining patients have long-term disease-free survival. To determine if there are molecular differences between primary tumors that predict prognosis, we performed RNA-seq on 47 macrodissected tumors from newly diagnosed patients with TNBC (n = 47; 22 relapse, 25 no relapse; follow-up median, 8 years; range, 2-11 years). We discovered that expression of the MHC class II (MHC II) antigen presentation pathway in tumor tissue was the most significant pathway associated with progression-free survival (HR, 0.36; log-rank P = 0.0098). The association between MHC II pathway expression and good prognosis was confirmed in a public gene expression database of 199 TNBC cases (HR, 0.28; log-rank P = 4.5 × 10(-8)). Further analysis of immunohistochemistry, laser-capture microdissected tumors, and TNBC cell lines demonstrated that tumor cells, in addition to immune cells, aberrantly express the MHC II pathway. MHC II pathway expression was also associated with B-cell and T-cell infiltration in the tumor. Together, these data support the model that aberrant expression of the MHC II pathway in TNBC tumor cells may trigger an antitumor immune response that reduces the rate of relapse and enhances progression-free survival. Cancer Immunol Res; 4(5); 390-9. ©2016 AACR.

摘要

三阴性乳腺癌(TNBC)是一种异质性患者结局的亚型。约 40%的患者经历快速复发,而其余患者则有长期无病生存。为了确定原发性肿瘤中是否存在预测预后的分子差异,我们对 47 例新诊断为 TNBC 的患者进行了 47 例宏切割肿瘤的 RNA-seq(n=47;22 例复发,25 例无复发;中位随访时间为 8 年;范围为 2-11 年)。我们发现肿瘤组织中 MHC Ⅱ类(MHC II)抗原呈递途径的表达是与无进展生存最显著相关的途径(HR,0.36;对数秩 P=0.0098)。在 199 例 TNBC 病例的公共基因表达数据库中,MHC II 途径表达与良好预后的相关性得到了证实(HR,0.28;对数秩 P=4.5×10(-8))。对免疫组化、激光捕获微切割肿瘤和 TNBC 细胞系的进一步分析表明,肿瘤细胞除了免疫细胞外,还异常表达 MHC II 途径。MHC II 途径的表达也与肿瘤中的 B 细胞和 T 细胞浸润有关。综上所述,这些数据支持这样的模型,即 TNBC 肿瘤细胞中 MHC II 途径的异常表达可能触发抗肿瘤免疫反应,从而降低复发率并增强无进展生存。Cancer Immunol Res; 4(5); 390-9. ©2016 AACR.

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