Identification of BIRC5 and HMMR as prognostic biomarkers for immune infiltration in prostate cancer.

IF 1.9 3区 医学 Q4 ANDROLOGY Translational andrology and urology Pub Date : 2024-11-30 Epub Date: 2024-11-28 DOI:10.21037/tau-24-359
Huarui Tang, Fanyang Zhou, Wentao Hu, Chen Zhang, Jianping Tao, Fawang Xing, Zhenxing Zhang, Yukui Gao
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Abstract

Background: Understanding the molecular mechanisms and identifying prognostic markers across various subtypes and stages of prostate cancer (PCa) are crucial for improving therapeutic strategies against the disease. This study focuses on discovering novel immune-related biomarkers that could aid in the evaluation and prognosis of PCa at different stages and serve as promising therapeutic targets.

Methods: Transcriptomic and clinical data from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) databases were analyzed to identify differentially expressed genes (DEGs) linked to PCa progression. The relationship between immune cell infiltration in the tumor microenvironment (TME) and the expression levels of baculoviral inhibitor of apoptosis protein repeat containing 5 (BIRC5) and hyaluronan-mediated motility receptor (HMMR) were examined using xCELL and quanTIseq algorithms.

Results: The analysis identified ten key hub genes, with survival analysis indicating that higher expressions of BIRC5 and HMMR were associated with poor outcomes and may contribute to tumor progression. Notably, the expressions of BIRC5 and HMMR showed a significant correlation with tumor-infiltrating lymphocytes (TILs) in various PCa subgroups. Immunohistochemistry (IHC) evaluations further corroborated the bioinformatics findings.

Conclusions: This study confirms BIRC5 and HMMR as potential biomarkers for predicting the prognosis of PCa, providing important evidence for the development of future therapeutic strategies. Through further research, these biomarkers may be utilized in clinical practice to improve patient management and treatment outcomes.

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BIRC5和HMMR作为前列腺癌免疫浸润预后生物标志物的鉴定
背景:了解前列腺癌(PCa)不同亚型和分期的分子机制和预后标志物对改善治疗策略至关重要。本研究的重点是发现新的免疫相关生物标志物,这些生物标志物可以帮助评估和预后不同阶段的前列腺癌,并作为有希望的治疗靶点。方法:分析来自Cancer Genome Atlas (TCGA)和Gene Expression Omnibus (GEO)数据库的转录组学和临床数据,以确定与PCa进展相关的差异表达基因(DEGs)。采用xCELL和quanTIseq算法检测肿瘤微环境免疫细胞浸润(TME)与杆状病毒凋亡蛋白重复抑制剂5 (BIRC5)和透明质酸介导的运动受体(HMMR)表达水平的关系。结果:该分析确定了10个关键枢纽基因,生存分析表明BIRC5和HMMR的高表达与不良预后相关,并可能导致肿瘤进展。值得注意的是,BIRC5和HMMR的表达与肿瘤浸润淋巴细胞(til)在各PCa亚组中均有显著相关性。免疫组织化学(IHC)评估进一步证实了生物信息学的发现。结论:本研究证实BIRC5和HMMR是预测前列腺癌预后的潜在生物标志物,为未来治疗策略的制定提供了重要依据。通过进一步的研究,这些生物标志物可用于临床实践,以改善患者的管理和治疗效果。
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来源期刊
CiteScore
4.10
自引率
5.00%
发文量
80
期刊介绍: ranslational Andrology and Urology (Print ISSN 2223-4683; Online ISSN 2223-4691; Transl Androl Urol; TAU) is an open access, peer-reviewed, bi-monthly journal (quarterly published from Mar.2012 - Dec. 2014). The main focus of the journal is to describe new findings in the field of translational research of Andrology and Urology, provides current and practical information on basic research and clinical investigations of Andrology and Urology. Specific areas of interest include, but not limited to, molecular study, pathology, biology and technical advances related to andrology and urology. Topics cover range from evaluation, prevention, diagnosis, therapy, prognosis, rehabilitation and future challenges to urology and andrology. Contributions pertinent to urology and andrology are also included from related fields such as public health, basic sciences, education, sociology, and nursing.
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