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

机译:MHC II类通路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

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摘要

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 x 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. (C) 2016 AACR.
机译:三阴性乳腺癌(TNBC)是患者结果异质性的亚型。大约40%的患者经历了快速复发,而其余患者则具有长期无病生存期。为了确定可预测预后的原发性肿瘤之间是否存在分子差异,我们对来自新诊断的TNBC患者的47例宏观解剖肿瘤进行了RNA测序(n = 47; 22复发,25无复发;随访中位数,8年;范围,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相关的最重要途径(HR,0.36;对数秩P = 0.0098)。 MHC II途径表达与良好预后之间的关联在199例TNBC病例的公共基因表达数据库中得到了证实(HR,0.28;对数秩P = 4.5 x 10(-8))。免疫组织化学,激光捕获显微切割的肿瘤和TNBC细胞系的进一步分析表明,除了免疫细胞外,肿瘤细胞还异常表达MHC II途径。 MHC II途径表达还与肿瘤中的B细胞和T细胞浸润有关。总之,这些数据支持了模型,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,从而降低复发率并提高无进展生存期。 (C)2016 AACR。

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