Androgens Modulate Tumor-Immune Interactions in Testicular Germ Cell Tumors.

IF 3.4 2区 医学 Q1 ANDROLOGY
Andrology Pub Date : 2026-09-29 DOI:10.1111/andr.70402
Ida Hamann, Lucas Klaus, Patrick Fruth, Alexander Fichtner, Tobias J Legler, Holger M Reichardt, Fabian A Gayer
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Abstract

Background: The majority of testicular germ cell tumors (TGCT) are derived from the germ cell neoplasia in situ and arise after puberty in the local presence of high levels of testosterone. The seminoma subtype features a rich inflammatory infiltrate which impacts tumor progression but the role of testosterone in shaping tumor-immune interactions is yet unknown.

Objective: We characterized androgen receptor and associated gene expression in the TGCT microenvironment and investigated the impact of dihydrotestosterone (DHT) on seminomatous tumor cells as well as stimulated T cells and monocytes. As an in vitro model of the seminoma microenvironment, cocultures of TCam-2 cells with immune cell subtypes were analyzed in the presence of DHT.

Material and methods: Gene expression was analyzed in tumorous and nontumorous tissue specimens from TGCT patients and TGCT cell lines. Bulk and single-cell RNA-sequencing data were used for validation. T cells and monocytes were isolated from the blood of healthy individuals and either activated in vitro or cocultured with TCam-2 cells. Proliferation and metabolic assays, quantitative RT-PCR, flow cytometry, and ELISA were employed to assess the impact of DHT on tumor and immune cells.

Results: Androgen receptor and related gene expression was demonstrated in tumorous tissue from patients, TGCT cell lines, and activated primary immune cells, which was supported by the analysis of published RNA-seq data sets. DHT exerted only a minor effect on TCam-2 cells, whereas hormone treatment markedly mitigated T cell and monocyte activation in a dose-dependent manner. In addition, DHT modulated immune cell activity and selected features of TCam-2 cells in T cell and monocyte cocultures serving as an in vitro model of the seminoma microenvironment.

Discussion and conclusion: Our results suggest that androgens present in tumorous testis of TGCT patients could impact tumor-immune interactions and thereby clinical outcome.

雄激素调节睾丸生殖细胞肿瘤的肿瘤免疫相互作用。
背景:大多数睾丸生殖细胞瘤(TGCT)来源于原位生殖细胞瘤,发生在青春期后,局部存在高水平睾丸激素。精原细胞瘤亚型具有丰富的炎症浸润,影响肿瘤进展,但睾酮在形成肿瘤免疫相互作用中的作用尚不清楚。目的:研究TGCT微环境中雄激素受体及相关基因的表达,探讨双氢睾酮(DHT)对半瘤性肿瘤细胞及受刺激的T细胞和单核细胞的影响。作为精原细胞瘤微环境的体外模型,我们分析了DHT存在下TCam-2细胞与免疫细胞亚型共培养的情况。材料和方法:分析TGCT患者肿瘤和非肿瘤组织标本及TGCT细胞系的基因表达。使用大量和单细胞rna测序数据进行验证。从健康个体的血液中分离出T细胞和单核细胞,在体外激活或与TCam-2细胞共培养。采用增殖和代谢试验、定量RT-PCR、流式细胞术和ELISA法评估DHT对肿瘤和免疫细胞的影响。结果:来自患者、TGCT细胞系和激活的原代免疫细胞的肿瘤组织中均存在雄激素受体及相关基因表达,已发表的RNA-seq数据集分析支持了这一结果。DHT仅对TCam-2细胞产生轻微影响,而激素治疗则以剂量依赖的方式显著减轻T细胞和单核细胞的活化。此外,DHT在T细胞和单核细胞共培养中调节免疫细胞活性和TCam-2细胞的选择特征,作为精原细胞瘤微环境的体外模型。讨论和结论:我们的研究结果表明,TGCT患者肿瘤睾丸中的雄激素可能影响肿瘤免疫相互作用,从而影响临床结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Andrology
Andrology ANDROLOGY-
CiteScore
9.10
自引率
6.70%
发文量
200
期刊介绍: Andrology is the study of the male reproductive system and other male gender related health issues. Andrology deals with basic and clinical aspects of the male reproductive system (gonads, endocrine and accessory organs) in all species, including the diagnosis and treatment of medical problems associated with sexual development, infertility, sexual dysfunction, sex hormone action and other urological problems. In medicine, Andrology as a specialty is a recent development, as it had previously been considered a subspecialty of urology or endocrinology
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