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Tasquinimod suppresses tumor cell growth and bone resorption by targeting immunosuppressive myeloid cells and inhibiting c-MYC expression in multiple myeloma

BACKGROUND: Immunotherapy emerged as a promising treatment option for multiple myeloma (MM) patients. However, therapeutic efficacy can be hampered by the presence of an immunosuppressive bone marrow microenvironment including myeloid cells. S100A9 was previously identified as a key regulator of mye...

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Autores principales: Fan, Rong, Satilmis, Hatice, Vandewalle, Niels, Verheye, Emma, Vlummens, Philip, Maes, Anke, Muylaert, Catharina, De Bruyne, Elke, Menu, Eline, Evans, Holly, Chantry, Andrew, De Beule, Nathan, Hose, Dirk, Törngren, Marie, Eriksson, Helena, Vanderkerken, Karin, Maes, Ken, Breckpot, Karine, De Veirman, Kim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9853259/
https://www.ncbi.nlm.nih.gov/pubmed/36650020
http://dx.doi.org/10.1136/jitc-2022-005319
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author Fan, Rong
Satilmis, Hatice
Vandewalle, Niels
Verheye, Emma
Vlummens, Philip
Maes, Anke
Muylaert, Catharina
De Bruyne, Elke
Menu, Eline
Evans, Holly
Chantry, Andrew
De Beule, Nathan
Hose, Dirk
Törngren, Marie
Eriksson, Helena
Vanderkerken, Karin
Maes, Ken
Breckpot, Karine
De Veirman, Kim
author_facet Fan, Rong
Satilmis, Hatice
Vandewalle, Niels
Verheye, Emma
Vlummens, Philip
Maes, Anke
Muylaert, Catharina
De Bruyne, Elke
Menu, Eline
Evans, Holly
Chantry, Andrew
De Beule, Nathan
Hose, Dirk
Törngren, Marie
Eriksson, Helena
Vanderkerken, Karin
Maes, Ken
Breckpot, Karine
De Veirman, Kim
author_sort Fan, Rong
collection PubMed
description BACKGROUND: Immunotherapy emerged as a promising treatment option for multiple myeloma (MM) patients. However, therapeutic efficacy can be hampered by the presence of an immunosuppressive bone marrow microenvironment including myeloid cells. S100A9 was previously identified as a key regulator of myeloid cell accumulation and suppressive activity. Tasquinimod, a small molecule inhibitor of S100A9, is currently in a phase Ib/IIa clinical trial in MM patients (NCT04405167). We aimed to gain more insights into its mechanisms of action both on the myeloma cells and the immune microenvironment. METHODS: We analyzed the effects of tasquinimod on MM cell viability, cell proliferation and downstream signaling pathways in vitro using RNA sequencing, real-time PCR, western blot analysis and multiparameter flow cytometry. Myeloid cells and T cells were cocultured at different ratios to assess tasquinimod-mediated immunomodulatory effects. The in vivo impact on immune cells (myeloid cell subsets, macrophages, dendritic cells), tumor load, survival and bone disease were elucidated using immunocompetent 5TMM models. RESULTS: Tasquinimod treatment significantly decreased myeloma cell proliferation and colony formation in vitro, associated with an inhibition of c-MYC and increased p27 expression. Tasquinimod-mediated targeting of the myeloid cell population resulted in increased T cell proliferation and functionality in vitro. Notably, short-term tasquinimod therapy of 5TMM mice significantly increased the total CD11b(+) cells and shifted this population toward a more immunostimulatory state, which resulted in less myeloid-mediated immunosuppression and increased T cell activation ex vivo. Tasquinimod significantly reduced the tumor load and increased the trabecular bone volume, which resulted in prolonged overall survival of MM-bearing mice in vivo. CONCLUSION: Our study provides novel insights in the dual therapeutic effects of the immunomodulator tasquinimod and fosters its evaluation in combination therapy trials for MM patients.
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spelling pubmed-98532592023-01-21 Tasquinimod suppresses tumor cell growth and bone resorption by targeting immunosuppressive myeloid cells and inhibiting c-MYC expression in multiple myeloma Fan, Rong Satilmis, Hatice Vandewalle, Niels Verheye, Emma Vlummens, Philip Maes, Anke Muylaert, Catharina De Bruyne, Elke Menu, Eline Evans, Holly Chantry, Andrew De Beule, Nathan Hose, Dirk Törngren, Marie Eriksson, Helena Vanderkerken, Karin Maes, Ken Breckpot, Karine De Veirman, Kim J Immunother Cancer Clinical/Translational Cancer Immunotherapy BACKGROUND: Immunotherapy emerged as a promising treatment option for multiple myeloma (MM) patients. However, therapeutic efficacy can be hampered by the presence of an immunosuppressive bone marrow microenvironment including myeloid cells. S100A9 was previously identified as a key regulator of myeloid cell accumulation and suppressive activity. Tasquinimod, a small molecule inhibitor of S100A9, is currently in a phase Ib/IIa clinical trial in MM patients (NCT04405167). We aimed to gain more insights into its mechanisms of action both on the myeloma cells and the immune microenvironment. METHODS: We analyzed the effects of tasquinimod on MM cell viability, cell proliferation and downstream signaling pathways in vitro using RNA sequencing, real-time PCR, western blot analysis and multiparameter flow cytometry. Myeloid cells and T cells were cocultured at different ratios to assess tasquinimod-mediated immunomodulatory effects. The in vivo impact on immune cells (myeloid cell subsets, macrophages, dendritic cells), tumor load, survival and bone disease were elucidated using immunocompetent 5TMM models. RESULTS: Tasquinimod treatment significantly decreased myeloma cell proliferation and colony formation in vitro, associated with an inhibition of c-MYC and increased p27 expression. Tasquinimod-mediated targeting of the myeloid cell population resulted in increased T cell proliferation and functionality in vitro. Notably, short-term tasquinimod therapy of 5TMM mice significantly increased the total CD11b(+) cells and shifted this population toward a more immunostimulatory state, which resulted in less myeloid-mediated immunosuppression and increased T cell activation ex vivo. Tasquinimod significantly reduced the tumor load and increased the trabecular bone volume, which resulted in prolonged overall survival of MM-bearing mice in vivo. CONCLUSION: Our study provides novel insights in the dual therapeutic effects of the immunomodulator tasquinimod and fosters its evaluation in combination therapy trials for MM patients. BMJ Publishing Group 2023-01-17 /pmc/articles/PMC9853259/ /pubmed/36650020 http://dx.doi.org/10.1136/jitc-2022-005319 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Clinical/Translational Cancer Immunotherapy
Fan, Rong
Satilmis, Hatice
Vandewalle, Niels
Verheye, Emma
Vlummens, Philip
Maes, Anke
Muylaert, Catharina
De Bruyne, Elke
Menu, Eline
Evans, Holly
Chantry, Andrew
De Beule, Nathan
Hose, Dirk
Törngren, Marie
Eriksson, Helena
Vanderkerken, Karin
Maes, Ken
Breckpot, Karine
De Veirman, Kim
Tasquinimod suppresses tumor cell growth and bone resorption by targeting immunosuppressive myeloid cells and inhibiting c-MYC expression in multiple myeloma
title Tasquinimod suppresses tumor cell growth and bone resorption by targeting immunosuppressive myeloid cells and inhibiting c-MYC expression in multiple myeloma
title_full Tasquinimod suppresses tumor cell growth and bone resorption by targeting immunosuppressive myeloid cells and inhibiting c-MYC expression in multiple myeloma
title_fullStr Tasquinimod suppresses tumor cell growth and bone resorption by targeting immunosuppressive myeloid cells and inhibiting c-MYC expression in multiple myeloma
title_full_unstemmed Tasquinimod suppresses tumor cell growth and bone resorption by targeting immunosuppressive myeloid cells and inhibiting c-MYC expression in multiple myeloma
title_short Tasquinimod suppresses tumor cell growth and bone resorption by targeting immunosuppressive myeloid cells and inhibiting c-MYC expression in multiple myeloma
title_sort tasquinimod suppresses tumor cell growth and bone resorption by targeting immunosuppressive myeloid cells and inhibiting c-myc expression in multiple myeloma
topic Clinical/Translational Cancer Immunotherapy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9853259/
https://www.ncbi.nlm.nih.gov/pubmed/36650020
http://dx.doi.org/10.1136/jitc-2022-005319
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