Metabolism-Related Signature Analysis Uncovers the Prognostic and Immunotherapeutic Characteristics of Renal Cell Carcinoma.
Metabolism-Related Signature Analysis Uncovers the Prognostic and Immunotherapeutic Characteristics of Renal Cell Carcinoma.
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代谢相关特征分析揭示肾细胞癌的预后和免疫治疗特征
DOI:
10.3389/fmolb.2022.837145
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发表时间:
2022
影响因子:
5
通讯作者:
Zhou L
中科院分区:
文献类型:
--
作者:
Zhang J;Zhang Q;Shi Y;Wang P;Gong Y;He S;Li Z;Feng N;Wang Y;Jiang P;Ci W;Li X;Zhou L
Renal cell carcinoma (RCC) is one of the most common urological cancers. RCC has a poor prognosis and is considered a metabolic disease. It has been reported that many metabolic pathways are associated with the development of RCC. However, the prognostic value of metabolism-related genes in RCC is unclear. We herein aimed to establish a scoring system based on the gene expression profile of metabolic genes to evaluate the response to immunotherapy and predict the prognosis of RCC. In this study, we collected multicentre RCC data and performed integrated analysis to characterize the role of tumour metabolism in RCC and explore the relationship between metabolism and prognosis and immune therapy. Based on transcriptomic data, metabolism-related genes were used for nonnegative matrix factorization clustering. We obtained three subclasses of RCC (M1, M2, and M3), and they are associated with different prognoses and immune infiltrate levels. Then, based on the pathway activity of 113 metabolism-related gene signatures, we classified patients into three distinct metabolism-related signatures. Finally, we provide a metabolism-related pathway score (MRPScore) that is significantly associated with RCC prognosis and the response to immunotherapy. Taken together, in this study, we established an RCC classification system based on metabolic gene expression profiles that could further the understanding of the diversity of RCC. We also present the MRPScore, which may be used as an indicator to predict the response to clinical immune therapy.
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影响因子:
23.4
作者:
Moch, Holger;Cubilla, Antonio L.;Ulbright, Thomas M.
通讯作者:
Ulbright, Thomas M.
影响因子:
64.8
作者:
Sreekumar, Arun;Poisson, Laila M.;Rajendiran, Thekkelnaycke M.;Khan, Amjad P.;Cao, Qi;Yu, Jindan;Laxman, Bharathi;Mehra, Rohit;Lonigro, Robert J.;Li, Yong;Nyati, Mukesh K.;Ahsan, Aarif;Kalyana-Sundaram, Shanker;Han, Bo;Cao, Xuhong;Byun, Jaeman;Omenn, Gilbert S.;Ghosh, Debashis;Pennathur, Subramaniam;Alexander, Danny C.;Berger, Alvin;Shuster, Jeffrey R.;Wei, John T.;Varambally, Sooryanarayana;Beecher, Christopher;Chinnaiyan, Arul M.
通讯作者:
Chinnaiyan, Arul M.
影响因子:
10.1
作者:
McKay RR;Bossé D;Xie W;Wankowicz SAM;Flaifel A;Brandao R;Lalani AA;Martini DJ;Wei XX;Braun DA;Van Allen E;Castellano D;De Velasco G;Wells JC;Heng DY;Fay AP;Schutz FA;Hsu J;Pal SK;Lee JL;Hsieh JJ;Harshman LC;Signoretti S;Motzer RJ;Feldman D;Choueiri TK
通讯作者:
Choueiri TK
影响因子:
10.5
作者:
Jaramillo MC;Zhang DD
通讯作者:
Zhang DD
影响因子:
11.2
作者:
Ganti S;Taylor SL;Abu Aboud O;Yang J;Evans C;Osier MV;Alexander DC;Kim K;Weiss RH
通讯作者:
Weiss RH