Identification of a differentiation-related prognostic nomogram based on single-cell RNA sequencing in clear cell renal cell carcinoma

被引:6
|
作者
Xia, Zhi-Nan [1 ]
Wu, Jing-Gen [2 ]
Yao, Wen-Hao [1 ]
Meng, Yu-Yang [1 ]
Jian, Wen-Gang [1 ]
Wang, Teng-Da [1 ]
Xue, Wei [1 ]
Yu, Yi-Peng [1 ]
Cai, Li-Cheng [1 ]
Wang, Xing-Yuan [1 ]
Zhang, Peng [1 ]
Li, Zhi-Yuan [1 ]
Zhou, Hao [3 ]
Jiang, Zhi-Cheng [3 ]
Zhou, Jia-Yu [4 ]
Zhang, Cheng [5 ]
机构
[1] Harbin Med Univ, Dept Urol, Affiliated Hosp 1, Harbin 150001, Peoples R China
[2] Zhejiang Univ, Dept Urol Androl, Womens Hosp, Sch Med, Hangzhou 310006, Peoples R China
[3] Zhejiang Univ, Dept Urol, Affiliated Hosp 4, Sch Med, Yiwu City 322000, Peoples R China
[4] Xinjiang Second Med Coll, Karamay City 834000, Peoples R China
[5] Zhejiang Univ, Sch Med, Hangzhou 310058, Peoples R China
基金
中国国家自然科学基金;
关键词
INTRATUMOR HETEROGENEITY; EVOLUTION; TUMOR; CHECKPOINT;
D O I
10.1038/s41598-022-15206-6
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Renal cell carcinoma (RCC) is a kidney cancer that is originated from the lined proximal convoluted tubule, and its major histological subtype is clear cell RCC (ccRCC). This study aimed to retrospectively analyze single-cell RNA sequencing (scRNA-seq) data from the Gene Expression Omnibus (GEO) database, to explore the correlation among the evolution of tumor microenvironment (TME), clinical outcomes, and potential immunotherapeutic responses in combination with bulk RNA-seq data from The Cancer Genome Atlas (TCGA) database, and to construct a differentiation-related genes (DRG)-based prognostic risk signature (PRS) and a nomogram to predict the prognosis of ccRCC patients. First, scRNA-seq data of ccRCC samples were systematically analyzed, and three subsets with distinct differentiation trajectories were identified. Then, ccRCC samples from TCGA database were divided into four DRG-based molecular subtypes, and it was revealed that the molecular subtypes were significantly correlated with prognosis, clinicopathological features, TME, and the expression levels of immune checkpoint genes (ICGs). A DRG-based PRS was constructed, and it was an independent prognostic factor, which could well predict the prognosis of ccRCC patients. Finally, we constructed a prognostic nomogram based on the PRS and clinicopathological characteristics, which exhibited a high accuracy and a robust predictive performance. This study highlighted the significance of trajectory differentiation of ccRCC cells and TME evolution in predicting clinical outcomes and potential immunotherapeutic responses of ccRCC patients, and the nomogram provided an intuitive and accurate method for predicting the prognosis of such patients.
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页数:14
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