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Targeting FMRP: A new window for cancer immunotherapy
FMRP is regulated by Myc and is highly expressed in a variety of human and mouse tumor tissues. FMRP recruits Treg and M2 macrophages to form an immunosuppressive tumor microenvironment by IL3, PROS1 and exosomes. FMRP‐KO up‐regulates tumor cell secretion of CCL7, which directly activates and recrui...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10030685/ https://www.ncbi.nlm.nih.gov/pubmed/36968189 http://dx.doi.org/10.1002/mco2.233 |
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author | Zhang, Yaguang Wu, Tong Han, Junhong |
author_facet | Zhang, Yaguang Wu, Tong Han, Junhong |
author_sort | Zhang, Yaguang |
collection | PubMed |
description | FMRP is regulated by Myc and is highly expressed in a variety of human and mouse tumor tissues. FMRP recruits Treg and M2 macrophages to form an immunosuppressive tumor microenvironment by IL3, PROS1 and exosomes. FMRP‐KO up‐regulates tumor cell secretion of CCL7, which directly activates and recruits CD8+ T cells. FMRP‐KO recruits CCR5 and CXCR4 receptor‐positive CD8 T cells indirectly by promoting M1 macrophages to secrete CCL5, CXCL9, and CXCL10. [Image: see text] |
format | Online Article Text |
id | pubmed-10030685 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100306852023-03-23 Targeting FMRP: A new window for cancer immunotherapy Zhang, Yaguang Wu, Tong Han, Junhong MedComm (2020) Highlights FMRP is regulated by Myc and is highly expressed in a variety of human and mouse tumor tissues. FMRP recruits Treg and M2 macrophages to form an immunosuppressive tumor microenvironment by IL3, PROS1 and exosomes. FMRP‐KO up‐regulates tumor cell secretion of CCL7, which directly activates and recruits CD8+ T cells. FMRP‐KO recruits CCR5 and CXCR4 receptor‐positive CD8 T cells indirectly by promoting M1 macrophages to secrete CCL5, CXCL9, and CXCL10. [Image: see text] John Wiley and Sons Inc. 2023-03-21 /pmc/articles/PMC10030685/ /pubmed/36968189 http://dx.doi.org/10.1002/mco2.233 Text en © 2023 The Authors. MedComm published by Sichuan International Medical Exchange & Promotion Association (SCIMEA) and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Highlights Zhang, Yaguang Wu, Tong Han, Junhong Targeting FMRP: A new window for cancer immunotherapy |
title | Targeting FMRP: A new window for cancer immunotherapy |
title_full | Targeting FMRP: A new window for cancer immunotherapy |
title_fullStr | Targeting FMRP: A new window for cancer immunotherapy |
title_full_unstemmed | Targeting FMRP: A new window for cancer immunotherapy |
title_short | Targeting FMRP: A new window for cancer immunotherapy |
title_sort | targeting fmrp: a new window for cancer immunotherapy |
topic | Highlights |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10030685/ https://www.ncbi.nlm.nih.gov/pubmed/36968189 http://dx.doi.org/10.1002/mco2.233 |
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