免疫系统
癌症
免疫疗法
癌症研究
免疫编辑
癌症免疫疗法
转录组
肿瘤微环境
表观遗传学
生物
免疫检查点
乳腺癌
医学
癌细胞
细胞
T细胞
体内
生物标志物
细胞毒性T细胞
免疫学
计算生物学
细胞生长
生物信息学
血管生成
黑色素瘤
前列腺癌
体外
癌症生物标志物
基因表达
作者
Jiajin Li,Zheng Qu,Dacheng Zhu,Ye Lu,Jiaxin Lu,Zhen Wu,Luxiao Zhang,Pengpeng Zhang,Yiqin Xia,Shengbin Pei
标识
DOI:10.1038/s41698-025-01097-z
摘要
Prostaglandin D2 synthase (PTGDS), a newly identified anti-tumor target, shows promise in inhibiting various cancers and plays significant roles in the tumor microenvironment and immune regulation, yet a comprehensive pan-cancer analysis of its expression and prognostic value remains lacking. This study used multi-omics data from public databases to assess PTGDS's expression, mutation, and modification in multiple cancers, integrated single-cell and spatial transcriptomic data to explore its relationship with immune cells, and conducted in vitro and in vivo experiments in breast cancer (BRCA). Results showed that PTGDS is significantly dysregulated in most cancers, with its expression associated with different outcomes depending on cancer type. It correlates with epigenetic and biological functions, and low expression in BRCA indicates poor prognosis. Overexpression of PTGDS can inhibit breast cancer cell proliferation and invasion, increase CD8+ T - cell activity, and enhance anti-tumor immunity. Combining it with anti-PD-L1 improves BRCA treatment. PTGDS is a potential prognostic biomarker and a novel immunotherapy target for BRCA.
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