Exploring BIRC family genes as prognostic biomarkers and therapeutic targets in prostate cancer.

IF 2.9 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM Discover. Oncology Pub Date : 2025-02-26 DOI:10.1007/s12672-025-02002-7
Xiao-Xiang Yu, Yi Liu, Zeng-Mi Mo, Rong-Jiang Luo, Wen-Kai Chen
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Abstract

The potential oncogenic role of Baculoviral inhibitor of apoptosis (IAP) Repeat-Containing (BIRC) genes in prostate cancer (PCa) has yet to be fully investigated. Two genes associated with disease recurrence, BIRC5 and BIRC7, were identified through survival analysis, and prostate cancer patients were categorized into two subtypes, C1 and C2, based on these genes. We performed survival analyses to assess the relationship between subtypes and the prognosis of PCa. Single-cell dataset analysis was used to identify specific cell types with enriched expression of BIRC family genes. Our findings show that BIRC5 and BIRC7 exhibit higher expression in PCa tissues compared to non-cancerous tissues. High expression of BIRC5 and BIRC7 independently correlates with an adverse prognosis in PCa. The analysis of mechanisms reveals that the differentially expressed genes impact signaling pathways associated with cancer and immunity. BIRC5/BIRC7 correlate with several immune cells infiltrating levels including T cells and macrophages. Furthermore, our research indicates that elevated expression of BIRC5 is associated with immune infiltration in PCa. These findings highlight the potential of BIRC5/BIRC7 or C1 subtype as prognostic biomarkers, offering new insights into possible targets for the development of therapeutic biomarkers and immunotherapeutic for PCa.

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探讨BIRC家族基因作为前列腺癌预后生物标志物和治疗靶点的作用。
杆状病毒细胞凋亡抑制剂(IAP)内含重复序列(BIRC)基因在前列腺癌(PCa)中的潜在致癌作用尚未得到充分研究。通过生存分析鉴定出与疾病复发相关的两个基因BIRC5和BIRC7,并根据这些基因将前列腺癌患者分为C1和C2两个亚型。我们通过生存分析来评估前列腺癌亚型与预后之间的关系。单细胞数据集分析用于鉴定BIRC家族基因富集表达的特定细胞类型。我们的研究结果表明,BIRC5和BIRC7在PCa组织中的表达高于非癌组织。BIRC5和BIRC7的高表达与前列腺癌的不良预后独立相关。机制分析表明,差异表达的基因影响与癌症和免疫相关的信号通路。BIRC5/BIRC7与包括T细胞和巨噬细胞在内的多种免疫细胞浸润水平相关。此外,我们的研究表明,BIRC5的表达升高与前列腺癌的免疫浸润有关。这些发现突出了BIRC5/BIRC7或C1亚型作为预后生物标志物的潜力,为PCa治疗性生物标志物和免疫治疗的可能靶点的开发提供了新的见解。
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来源期刊
Discover. Oncology
Discover. Oncology Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
2.40
自引率
9.10%
发文量
122
审稿时长
5 weeks
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