USP14 promotes tryptophan metabolism and immune suppression by stabilizing IDO1 in colorectal cancer

IDO1-mediated tryptophan metabolism plays an important role in creating an immunosuppressive tumour microenvironment. Here, the authors show that deubiquitinase USP14 regulates immune suppression by inducing IDO1 stabilization and suggest USP14 as a potential therapeutic target to improve immunother...

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Main Authors: Dongni Shi, Xianqiu Wu, Yunting Jian, Junye Wang, Chengmei Huang, Shuang Mo, Yue Li, Fengtian Li, Chao Zhang, Dongsheng Zhang, Huizhong Zhang, Huilin Huang, Xin Chen, Y. Alan Wang, Chuyong Lin, Guozhen Liu, Libing Song, Wenting Liao
Format: Article
Language:English
Published: Nature Portfolio 2022-09-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-022-33285-x
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author Dongni Shi
Xianqiu Wu
Yunting Jian
Junye Wang
Chengmei Huang
Shuang Mo
Yue Li
Fengtian Li
Chao Zhang
Dongsheng Zhang
Huizhong Zhang
Huilin Huang
Xin Chen
Y. Alan Wang
Chuyong Lin
Guozhen Liu
Libing Song
Wenting Liao
author_facet Dongni Shi
Xianqiu Wu
Yunting Jian
Junye Wang
Chengmei Huang
Shuang Mo
Yue Li
Fengtian Li
Chao Zhang
Dongsheng Zhang
Huizhong Zhang
Huilin Huang
Xin Chen
Y. Alan Wang
Chuyong Lin
Guozhen Liu
Libing Song
Wenting Liao
author_sort Dongni Shi
collection DOAJ
description IDO1-mediated tryptophan metabolism plays an important role in creating an immunosuppressive tumour microenvironment. Here, the authors show that deubiquitinase USP14 regulates immune suppression by inducing IDO1 stabilization and suggest USP14 as a potential therapeutic target to improve immunotherapy in colorectal cancer.
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spelling doaj.art-da0e7849fcb34a24976064852f9e4e8c2022-12-22T03:24:21ZengNature PortfolioNature Communications2041-17232022-09-0113111810.1038/s41467-022-33285-xUSP14 promotes tryptophan metabolism and immune suppression by stabilizing IDO1 in colorectal cancerDongni Shi0Xianqiu Wu1Yunting Jian2Junye Wang3Chengmei Huang4Shuang Mo5Yue Li6Fengtian Li7Chao Zhang8Dongsheng Zhang9Huizhong Zhang10Huilin Huang11Xin Chen12Y. Alan Wang13Chuyong Lin14Guozhen Liu15Libing Song16Wenting Liao17Department of Experimental Research, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer MedicineDepartment of Experimental Research, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer MedicineDepartment of Experimental Research, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer MedicineDepartment of Thoracic Surgery, Sun Yat-Sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer MedicineDepartment of Experimental Research, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer MedicineDepartment of Biochemistry, Zhongshan School of Medicine, Sun Yat-sen UniversityDepartment of Experimental Research, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer MedicineDepartment of Experimental Research, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer MedicineDepartment of Pathology, Sun Yat-sen University Cancer CenterDepartment of Medical Oncology, Sun Yat-sen University Cancer CenterDepartment of Pathology, Sun Yat-sen University Cancer CenterDepartment of Experimental Research, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer MedicineKey Laboratory of Protein Modification and Degradation, School of Basic Medical Sciences, Guangzhou Institute of Oncology, Tumor Hospital, Guangzhou Medical UniversityBrown Center for Immunotherapy, Department of Medicine, Indiana University School of Medicine, Indiana University Melvin and Bren Simon Comprehensive Cancer CenterDepartment of Experimental Research, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer MedicineSchool of Life and Health Sciences, The Chinese University of Hong KongDepartment of Experimental Research, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer MedicineDepartment of Experimental Research, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer MedicineIDO1-mediated tryptophan metabolism plays an important role in creating an immunosuppressive tumour microenvironment. Here, the authors show that deubiquitinase USP14 regulates immune suppression by inducing IDO1 stabilization and suggest USP14 as a potential therapeutic target to improve immunotherapy in colorectal cancer.https://doi.org/10.1038/s41467-022-33285-x
spellingShingle Dongni Shi
Xianqiu Wu
Yunting Jian
Junye Wang
Chengmei Huang
Shuang Mo
Yue Li
Fengtian Li
Chao Zhang
Dongsheng Zhang
Huizhong Zhang
Huilin Huang
Xin Chen
Y. Alan Wang
Chuyong Lin
Guozhen Liu
Libing Song
Wenting Liao
USP14 promotes tryptophan metabolism and immune suppression by stabilizing IDO1 in colorectal cancer
Nature Communications
title USP14 promotes tryptophan metabolism and immune suppression by stabilizing IDO1 in colorectal cancer
title_full USP14 promotes tryptophan metabolism and immune suppression by stabilizing IDO1 in colorectal cancer
title_fullStr USP14 promotes tryptophan metabolism and immune suppression by stabilizing IDO1 in colorectal cancer
title_full_unstemmed USP14 promotes tryptophan metabolism and immune suppression by stabilizing IDO1 in colorectal cancer
title_short USP14 promotes tryptophan metabolism and immune suppression by stabilizing IDO1 in colorectal cancer
title_sort usp14 promotes tryptophan metabolism and immune suppression by stabilizing ido1 in colorectal cancer
url https://doi.org/10.1038/s41467-022-33285-x
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