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Construction and validation of an immunity-related prognostic signature for breast cancer

机译:乳腺癌免疫相关预后签名的构建与验证

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摘要

Breast cancer is one of the most lethal malignancies among women, and understanding the effects of host immunity on disease progression offers the potential to improve immunotherapies against it. Here, we constructed an immunity-related gene (IRG)-based prognostic signature to stratify breast cancer patients and predict their survival. We identified differentially-expressed genes by analyzing the breast cancer transcriptome data from The Cancer Genome Atlas. Univariate Cox regression revealed 179 survival-correlated IRGs, 12 of which we used to construct an immunity-based prognostic signature that stratified breast cancer patients into high- and low-risk groups. The signature was an independent predictor for survival and was validated in an independent dataset. We also investigated the correlations between our prognostic signature and immune infiltrates and found that signature-derived risk scores correlated negatively with infiltration of B cells, CD4+ T cells, CD8+ T cells, neutrophils and dendritic cells. Our results show that the proposed prognostic signature reflects the tumor immune microenvironment, which makes it a potential indicator for survival that warrants further research to assess its clinical utility.
机译:乳腺癌是女性中最致命的恶性肿瘤之一,并且了解宿主免疫性对疾病进展的影响提供了改善免疫治疗IT的潜力。在这里,我们构建了与基于预后签名的免疫相关基因(IRG),以分层乳腺癌患者并预测其存活率。通过从癌症基因组地图集分析乳腺癌转录组数据,我们鉴定了差异表达的基因。单变量Cox回归揭示了179个生存相关的IRGS,其中12个我们用于构建基于免疫的预后签名,将乳腺癌患者分析为高风险群体。签名是生存的独立预测因子,并在独立数据集中验证。我们还研究了我们的预后签名和免疫浸润之间的相关性,发现签名衍生的风险评分与B细胞,CD4 + T细胞,CD8 + T细胞,中性粒细胞和树枝状细胞的浸润负相关。我们的研究结果表明,所提出的预后签名反映了肿瘤免疫微环境,使其成为存活率的潜在指标,以便进一步研究评估其临床效用。

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