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Expression of X-Linked Inhibitor of Apoptosis Protein (XIAP) in Breast Cancer Is Associated with Shorter Survival and Resistance to Chemotherapy

机译:乳腺癌中凋亡蛋白(XIAP)的表达与较短的存活和化疗抗性相关

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摘要

The X-linked inhibitor of apoptosis protein (XIAP) is considered the most potent inhibitor of cell death, and it is well established that XIAP promotes resistance to chemotherapy, radiation, and anti-cancer immune responses. This study evaluates the correlations between XIAP expression and clinicopathological features, including disease-free survival (DFS) and pathological complete response (pCR) to chemotherapy, in more than 2300 invasive primary breast cancer samples. We found a significant association of XIAP expression with younger patients’ age (≤50 years), pathological ductal type, lower tumor grade, node-positive status, and PAM50 luminal B subtype. Analysis of molecular subtypes revealed a stronger prognostic value in HR+/HER2− tumors. Higher XIAP expression was associated with shorter DFS and lower pCR rate to chemotherapy in both uni- and multivariate analyses. All these correlations were observed at both the RNA and protein level, indicating the potential of XIAP as a promising therapeutic target in primary invasive breast cancer.
机译:癫痫蛋白(XIAP)的X链接抑制剂被认为是最有效的细胞死亡抑制剂,并且很好地确定了XIAP促进对化疗,辐射和抗癌免疫反应的抵抗力。本研究评估了XIAP表达和临床病理学特征之间的相关性,包括无病生存(DFS)和病理完全反应(PCR)化疗,在2300多种侵袭性原发性乳腺癌样品中。我们发现XIAP表达与年轻患者年龄(≤50岁),病理导管型,下肿瘤等级,节点阳性状态和PAM50腔B亚型的重大关联。分子亚型分析显示HR + / HER2-肿瘤中的更强预后值。在单一和多变量分析中,较高的XIAP表达与较短的DFS和降低PCR率降低到化疗。在RNA和蛋白质水平中观察到所有这些相关性,表明XIAP作为主要侵入性乳腺癌中有希望的治疗靶标的潜力。

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