Machine learning-based risk model incorporating tumor immune and stromal contexture predicts cancer prognosis and immunotherapy efficacy.
Machine learning-based risk model incorporating tumor immune and stromal contexture predicts cancer prognosis and immunotherapy efficacy.
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DOI:
10.1016/j.isci.2023.107058
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发表时间:
2023-07-21
期刊:
影响因子:
5.8
通讯作者:
Hong, Shaodong
中科院分区:
文献类型:
--
作者:
He, Li-Na;Li, Haifeng;Du, Wei;Fu, Sha;Luo, Linfeng;Chen, Tao;Zhang, Xuanye;Chen, Chen;Jiang, Yongluo;Wang, Yixing;Wang, Yuhong;Yu, Hui;Zhou, Yixin;Lin, Zuan;Zhao, Yuanyuan;Huang, Yan;Zhao, Hongyun;Fang, Wenfeng;Yang, Yunpeng;Zhang, Li;Hong, Shaodong
The immune and stromal contexture within the tumor microenvironment (TME) interact with cancer cells and jointly determine disease process and therapeutic response. We aimed at developing a risk scoring model based on TME-related genes of squamous cell lung cancer to predict patient prognosis and immunotherapeutic response. TME-related genes were identified through exploring genes that correlated with immune scores and stromal scores. LASSO-Cox regression model was used to establish the TME-related risk scoring (TMErisk) model. A TMErisk model containing six genes was established. High TMErisk correlated with unfavorable OS in LUSC patients and this association was validated in multiple NSCLC datasets. Genes involved in pathways associated with immunosuppressive microenvironment were enriched in the high TMErisk group. Tumors with high TMErisk showed elevated infiltration of immunosuppressive cells. High TMErisk predicted worse immunotherapeutic response and prognosis across multiple carcinomas. TMErisk model could serve as a robust biomarker for predicting OS and immunotherapeutic response. A TMErisk model was established based on six immune/stroma-related genes High TMErisk predicts poor prognosis and immunotherapy efficacy in multiple cancers High TMErisk correlated with immune-suppressive tumor micro-milieu TMErisk outperformed PD-L1 and TMB in predicting immunotherapy efficacy Biological sciences; Immunology; Cancer; Machine learning
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影响因子:
9.5
作者:
Maeser, Danielle;Gruener, Robert F.;Huang, Rong Stephanie
通讯作者:
Huang, Rong Stephanie
影响因子:
12.4
作者:
Choi H;Na KJ
通讯作者:
Na KJ
影响因子:
3
作者:
Langfelder P;Horvath S
通讯作者:
Horvath S
影响因子:
64.5
作者:
Basu A;Bodycombe NE;Cheah JH;Price EV;Liu K;Schaefer GI;Ebright RY;Stewart ML;Ito D;Wang S;Bracha AL;Liefeld T;Wawer M;Gilbert JC;Wilson AJ;Stransky N;Kryukov GV;Dancik V;Barretina J;Garraway LA;Hon CS;Munoz B;Bittker JA;Stockwell BR;Khabele D;Stern AM;Clemons PA;Shamji AF;Schreiber SL
通讯作者:
Schreiber SL
影响因子:
82.9
作者:
Binnewies M;Roberts EW;Kersten K;Chan V;Fearon DF;Merad M;Coussens LM;Gabrilovich DI;Ostrand-Rosenberg S;Hedrick CC;Vonderheide RH;Pittet MJ;Jain RK;Zou W;Howcroft TK;Woodhouse EC;Weinberg RA;Krummel MF
通讯作者:
Krummel MF