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E3 ligase FBXW7 restricts M2-like tumor-associated macrophage polarization by targeting c-Myc

FBXW7 functions as an E3 ubiquitin ligase to mediate oncoprotein degradation via the ubiquitin-proteasome system in cancer cells, effectively inhibiting the growth and survival of tumor cells. However, little is known about the functions of FBXW7 in macrophages and the tumor immune microenvironment....

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Autores principales: Zhong, Lijia, Zhang, Yuanyuan, Li, Mengyao, Song, Yinjing, Liu, Danhui, Yang, Xin, Yang, Dehua, Qu, Hao, Lai, Lihua, Wang, Qingqing, Chen, Zhimin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7762499/
https://www.ncbi.nlm.nih.gov/pubmed/33260160
http://dx.doi.org/10.18632/aging.202293
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author Zhong, Lijia
Zhang, Yuanyuan
Li, Mengyao
Song, Yinjing
Liu, Danhui
Yang, Xin
Yang, Dehua
Qu, Hao
Lai, Lihua
Wang, Qingqing
Chen, Zhimin
author_facet Zhong, Lijia
Zhang, Yuanyuan
Li, Mengyao
Song, Yinjing
Liu, Danhui
Yang, Xin
Yang, Dehua
Qu, Hao
Lai, Lihua
Wang, Qingqing
Chen, Zhimin
author_sort Zhong, Lijia
collection PubMed
description FBXW7 functions as an E3 ubiquitin ligase to mediate oncoprotein degradation via the ubiquitin-proteasome system in cancer cells, effectively inhibiting the growth and survival of tumor cells. However, little is known about the functions of FBXW7 in macrophages and the tumor immune microenvironment. In this study, we find that FBXW7 suppresses M2-like tumor-associated macrophage (TAM) polarization to limit tumor progression. We identified a significant increase in the proportion of M2-like TAMs and aggravated tumor growth in mice with myeloid FBXW7 deficiency by subcutaneous inoculation with Lewis lung carcinoma cells (LLCs). When stimulated with LLCs supernatant in vitro, FBXW7-knockout macrophages displayed increased M2 macrophage polarization and enhanced ability of supporting cancer cells growth. In mechanism, we confirmed that FBXW7 inhibited M2-like TAM polarization by mediating c-Myc degradation via the ubiquitin-proteasome system. These findings highlight the role of FBXW7 in M2-like TAM polarization and provide new insights into the potential targets for cancer immunotherapies.
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spelling pubmed-77624992021-01-08 E3 ligase FBXW7 restricts M2-like tumor-associated macrophage polarization by targeting c-Myc Zhong, Lijia Zhang, Yuanyuan Li, Mengyao Song, Yinjing Liu, Danhui Yang, Xin Yang, Dehua Qu, Hao Lai, Lihua Wang, Qingqing Chen, Zhimin Aging (Albany NY) Research Paper FBXW7 functions as an E3 ubiquitin ligase to mediate oncoprotein degradation via the ubiquitin-proteasome system in cancer cells, effectively inhibiting the growth and survival of tumor cells. However, little is known about the functions of FBXW7 in macrophages and the tumor immune microenvironment. In this study, we find that FBXW7 suppresses M2-like tumor-associated macrophage (TAM) polarization to limit tumor progression. We identified a significant increase in the proportion of M2-like TAMs and aggravated tumor growth in mice with myeloid FBXW7 deficiency by subcutaneous inoculation with Lewis lung carcinoma cells (LLCs). When stimulated with LLCs supernatant in vitro, FBXW7-knockout macrophages displayed increased M2 macrophage polarization and enhanced ability of supporting cancer cells growth. In mechanism, we confirmed that FBXW7 inhibited M2-like TAM polarization by mediating c-Myc degradation via the ubiquitin-proteasome system. These findings highlight the role of FBXW7 in M2-like TAM polarization and provide new insights into the potential targets for cancer immunotherapies. Impact Journals 2020-12-01 /pmc/articles/PMC7762499/ /pubmed/33260160 http://dx.doi.org/10.18632/aging.202293 Text en Copyright: © 2020 Zhong et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Zhong, Lijia
Zhang, Yuanyuan
Li, Mengyao
Song, Yinjing
Liu, Danhui
Yang, Xin
Yang, Dehua
Qu, Hao
Lai, Lihua
Wang, Qingqing
Chen, Zhimin
E3 ligase FBXW7 restricts M2-like tumor-associated macrophage polarization by targeting c-Myc
title E3 ligase FBXW7 restricts M2-like tumor-associated macrophage polarization by targeting c-Myc
title_full E3 ligase FBXW7 restricts M2-like tumor-associated macrophage polarization by targeting c-Myc
title_fullStr E3 ligase FBXW7 restricts M2-like tumor-associated macrophage polarization by targeting c-Myc
title_full_unstemmed E3 ligase FBXW7 restricts M2-like tumor-associated macrophage polarization by targeting c-Myc
title_short E3 ligase FBXW7 restricts M2-like tumor-associated macrophage polarization by targeting c-Myc
title_sort e3 ligase fbxw7 restricts m2-like tumor-associated macrophage polarization by targeting c-myc
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7762499/
https://www.ncbi.nlm.nih.gov/pubmed/33260160
http://dx.doi.org/10.18632/aging.202293
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