Crosstalk between the CBM complex/NF-κB and MAPK/P27 signaling pathways of regulatory T cells contributes to the tumor microenvironment

Regulatory T cells (Tregs), which execute their immunosuppressive functions by multiple mechanisms, have been verified to contribute to the tumor microenvironment (TME). Numerous studies have shown that the activation of the CBM complex/NF-κB signaling pathway results in the expression of hypoxia-in...

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Main Authors: Tongbing Qi, Ying Luo, Weitong Cui, Yue Zhou, Xuan Ma, Dongming Wang, Xuewen Tian, Qinglu Wang
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-07-01
Series:Frontiers in Cell and Developmental Biology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fcell.2022.911811/full
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author Tongbing Qi
Tongbing Qi
Ying Luo
Weitong Cui
Yue Zhou
Xuan Ma
Dongming Wang
Xuewen Tian
Qinglu Wang
Qinglu Wang
author_facet Tongbing Qi
Tongbing Qi
Ying Luo
Weitong Cui
Yue Zhou
Xuan Ma
Dongming Wang
Xuewen Tian
Qinglu Wang
Qinglu Wang
author_sort Tongbing Qi
collection DOAJ
description Regulatory T cells (Tregs), which execute their immunosuppressive functions by multiple mechanisms, have been verified to contribute to the tumor microenvironment (TME). Numerous studies have shown that the activation of the CBM complex/NF-κB signaling pathway results in the expression of hypoxia-inducible factor-1 (HIF-1α) and interleukin-6 (IL-6), which initiate the TME formation. HIF-1α and IL-6 promote regulatory T cells (Tregs) proliferation and migration through the MAPK/CDK4/6/Rb and STAT3/SIAH2/P27 signaling pathways, respectively. IL-6 also promotes the production of HIF-1α and enhances the self-regulation of Tregs in the process of tumor microenvironment (TME) formation. In this review, we discuss how the crosstalk between the CARMA1–BCL10–MALT1 signalosome complex (CBM complex)/NF-κB and MAPK/P27 signaling pathways contributes to the formation of the TME, which may provide evidence for potential therapeutic targets in the treatment of solid tumors.
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spelling doaj.art-fff4b6ee87bb4286be031a0a57d1c4c82022-12-22T00:43:06ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2022-07-011010.3389/fcell.2022.911811911811Crosstalk between the CBM complex/NF-κB and MAPK/P27 signaling pathways of regulatory T cells contributes to the tumor microenvironmentTongbing Qi0Tongbing Qi1Ying Luo2Weitong Cui3Yue Zhou4Xuan Ma5Dongming Wang6Xuewen Tian7Qinglu Wang8Qinglu Wang9College of Sport and Health, Shandong Sport University, Jinan, ChinaKey Laboratory of Biomedical Engineering and Technology of Shandong High School, Qilu Medical University, Zibo, ChinaClinical Laboratory, Zibo Central Hospital, Zibo, ChinaKey Laboratory of Biomedical Engineering and Technology of Shandong High School, Qilu Medical University, Zibo, ChinaKey Laboratory of Biomedical Engineering and Technology of Shandong High School, Qilu Medical University, Zibo, ChinaKey Laboratory of Biomedical Engineering and Technology of Shandong High School, Qilu Medical University, Zibo, ChinaDepartment of Pediatrics, People’s Hospital of Huantai, Zibo, ChinaCollege of Sport and Health, Shandong Sport University, Jinan, ChinaCollege of Sport and Health, Shandong Sport University, Jinan, ChinaKey Laboratory of Biomedical Engineering and Technology of Shandong High School, Qilu Medical University, Zibo, ChinaRegulatory T cells (Tregs), which execute their immunosuppressive functions by multiple mechanisms, have been verified to contribute to the tumor microenvironment (TME). Numerous studies have shown that the activation of the CBM complex/NF-κB signaling pathway results in the expression of hypoxia-inducible factor-1 (HIF-1α) and interleukin-6 (IL-6), which initiate the TME formation. HIF-1α and IL-6 promote regulatory T cells (Tregs) proliferation and migration through the MAPK/CDK4/6/Rb and STAT3/SIAH2/P27 signaling pathways, respectively. IL-6 also promotes the production of HIF-1α and enhances the self-regulation of Tregs in the process of tumor microenvironment (TME) formation. In this review, we discuss how the crosstalk between the CARMA1–BCL10–MALT1 signalosome complex (CBM complex)/NF-κB and MAPK/P27 signaling pathways contributes to the formation of the TME, which may provide evidence for potential therapeutic targets in the treatment of solid tumors.https://www.frontiersin.org/articles/10.3389/fcell.2022.911811/fullregulatory T cellstumor microenvironmentCBM signaling pathwayMAPK/P27 signaling pathwayCARMA1
spellingShingle Tongbing Qi
Tongbing Qi
Ying Luo
Weitong Cui
Yue Zhou
Xuan Ma
Dongming Wang
Xuewen Tian
Qinglu Wang
Qinglu Wang
Crosstalk between the CBM complex/NF-κB and MAPK/P27 signaling pathways of regulatory T cells contributes to the tumor microenvironment
Frontiers in Cell and Developmental Biology
regulatory T cells
tumor microenvironment
CBM signaling pathway
MAPK/P27 signaling pathway
CARMA1
title Crosstalk between the CBM complex/NF-κB and MAPK/P27 signaling pathways of regulatory T cells contributes to the tumor microenvironment
title_full Crosstalk between the CBM complex/NF-κB and MAPK/P27 signaling pathways of regulatory T cells contributes to the tumor microenvironment
title_fullStr Crosstalk between the CBM complex/NF-κB and MAPK/P27 signaling pathways of regulatory T cells contributes to the tumor microenvironment
title_full_unstemmed Crosstalk between the CBM complex/NF-κB and MAPK/P27 signaling pathways of regulatory T cells contributes to the tumor microenvironment
title_short Crosstalk between the CBM complex/NF-κB and MAPK/P27 signaling pathways of regulatory T cells contributes to the tumor microenvironment
title_sort crosstalk between the cbm complex nf κb and mapk p27 signaling pathways of regulatory t cells contributes to the tumor microenvironment
topic regulatory T cells
tumor microenvironment
CBM signaling pathway
MAPK/P27 signaling pathway
CARMA1
url https://www.frontiersin.org/articles/10.3389/fcell.2022.911811/full
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