Construction and validation of a regulatory T cells-based classification of renal cell carcinoma: an integrated bioinformatic analysis and clinical cohort study

肾细胞癌 比例危险模型 队列 肿瘤科 医学 肾透明细胞癌 内科学 免疫疗法 多元分析 舒尼替尼 免疫组织化学 癌症
作者
Yuntao Yao,Yifan Liu,Bing-Nan Lu,Guo Ji,Lei Wang,Keqin Dong,Zihui Zhao,Donghao Lyu,Maodong Wei,Sanfang Tu,Xukun Lyu,Yuanan Li,Runzhi Huang,Zhou Wang,Guofeng Xu,Xiuwu Pan,Xingang Cui
出处
期刊:Cellular oncology [Springer Nature]
标识
DOI:10.1007/s13402-024-01030-9
摘要

Renal cell carcinoma (RCC), exhibiting remarkable heterogeneity, can be highly infiltrated by regulatory T cells (Tregs). However, the relationship between Treg and the heterogeneity of RCC remains to be explored. We acquired single-cell RNA-seq profiles and 537 bulk RNA-seq profiles of TCGA-KIRC cohort. Through clustering, monocle2 pseudotime and prognostic analyses, we identified Treg states-related prognostic genes (TSRPGs), then constructing the RCC Treg states-related prognostic classification (RCC-TSC). We also explored its prognostic significance and multi-omics landmarks. Additionally, we utilized correlation analysis to establish regulatory networks, and predicted candidate inhibitors. More importantly, in Xinhua cohort of 370 patients with kidney neoplasm, we used immunohistochemical (IHC) staining for classification, then employing statistical analyses including Chi-square tests and multivariate Cox proportional hazards regression analysis to explore its clinical relevance. We defined 44 TSRPGs in four different monocle states, and identified high immune infiltration RCC (HIRC, LAG3+, Mki67+) as the highly exhausted subtype with the worst prognosis in RCC-TSC (p < 0.001). BATF-LAG3-immune cells axis might be its underlying metastasis-related mechanism. Immunotherapy and inhibitors including sunitinib potentially conferred best therapeutic effects for HIRC. Furthermore, we successfully validated HIRC subtype as an independent prognostic factor within the Xinhua cohort (OS, HR = 16.68, 95% CI = 1.88–148.1, p = 0.011; PFS, HR = 4.43, 95% CI = 1.55–12.6, p = 0.005). Through integrated bioinformatics analysis and a large-sample retrospective clinical study, we successfully established RCC-TSC and a diagnostic kit, which could stratify RCC patients with different prognosis and to guide personalized treatment. Utilizing integrated bioinformatics analyses and a large-sample retrospective clinical study, a Treg states-related RCC prognostic classification is successfully established, which could stratify RCC patients with different prognosis and to guide personalized treatment.

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