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Targeting Cellular Iron Homeostasis with Ironomycin in Diffuse Large B-cell Lymphoma
Diffuse large B-cell lymphoma (DLBCL) is the most common hematological malignancy. Although more than half of patients with DLBCL achieve long-term remission, the majority of remaining patients succumb to the disease. As abnormal iron homeostasis is implicated in carcinogenesis and the progression o...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for Cancer Research
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9359736/ https://www.ncbi.nlm.nih.gov/pubmed/35078814 http://dx.doi.org/10.1158/0008-5472.CAN-21-0218 |
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author | Devin, Julie Cañeque, Tatiana Lin, Yea-Lih Mondoulet, Lucie Veyrune, Jean-Luc Abouladze, Matthieu Garcia De Paco, Elvira Karmous Gadacha, Ouissem Cartron, Guillaume Pasero, Philippe Bret, Caroline Rodriguez, Raphaël Moreaux, Jerome |
author_facet | Devin, Julie Cañeque, Tatiana Lin, Yea-Lih Mondoulet, Lucie Veyrune, Jean-Luc Abouladze, Matthieu Garcia De Paco, Elvira Karmous Gadacha, Ouissem Cartron, Guillaume Pasero, Philippe Bret, Caroline Rodriguez, Raphaël Moreaux, Jerome |
author_sort | Devin, Julie |
collection | PubMed |
description | Diffuse large B-cell lymphoma (DLBCL) is the most common hematological malignancy. Although more than half of patients with DLBCL achieve long-term remission, the majority of remaining patients succumb to the disease. As abnormal iron homeostasis is implicated in carcinogenesis and the progression of many tumors, we searched for alterations in iron metabolism in DLBCL that could be exploited to develop novel therapeutic strategies. Analysis of the iron metabolism gene expression profile of large cohorts of patients with DLBCL established the iron score (IS), a gene expression–based risk score enabling identification of patients with DLBCL with a poor outcome who might benefit from a suitable targeted therapy. In a panel of 16 DLBCL cell lines, ironomycin, a promising lysosomal iron-targeting small molecule, inhibited DLBCL cell proliferation at nanomolar concentrations compared with typical iron chelators. Ironomycin also induced significant cell growth inhibition, ferroptosis, and autophagy. Ironomycin treatment resulted in accumulation of DNA double-strand breaks, delayed progression of replication forks, and increased RPA2 phosphorylation, a marker of replication stress. Ironomycin significantly reduced the median number of viable primary DLBCL cells of patients without major toxicity for nontumor cells from the microenvironment and presented low toxicity in hematopoietic progenitors compared with conventional treatments. Significant synergistic effects were also observed by combining ironomycin with doxorubicin, BH3 mimetics, BTK inhibitors, or Syk inhibitors. Altogether, these data demonstrate that a subgroup of high-risk patients with DLBCL can be identified with the IS that can potentially benefit from targeting iron homeostasis. SIGNIFICANCE: Iron homeostasis represents a potential therapeutic target for high-risk patients with DLBCL that can be targeted with ironomycin to induce cell death and to sensitize tumor cells to conventional treatments. |
format | Online Article Text |
id | pubmed-9359736 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for Cancer Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-93597362023-01-05 Targeting Cellular Iron Homeostasis with Ironomycin in Diffuse Large B-cell Lymphoma Devin, Julie Cañeque, Tatiana Lin, Yea-Lih Mondoulet, Lucie Veyrune, Jean-Luc Abouladze, Matthieu Garcia De Paco, Elvira Karmous Gadacha, Ouissem Cartron, Guillaume Pasero, Philippe Bret, Caroline Rodriguez, Raphaël Moreaux, Jerome Cancer Res Metabolism and Chemical Biology Diffuse large B-cell lymphoma (DLBCL) is the most common hematological malignancy. Although more than half of patients with DLBCL achieve long-term remission, the majority of remaining patients succumb to the disease. As abnormal iron homeostasis is implicated in carcinogenesis and the progression of many tumors, we searched for alterations in iron metabolism in DLBCL that could be exploited to develop novel therapeutic strategies. Analysis of the iron metabolism gene expression profile of large cohorts of patients with DLBCL established the iron score (IS), a gene expression–based risk score enabling identification of patients with DLBCL with a poor outcome who might benefit from a suitable targeted therapy. In a panel of 16 DLBCL cell lines, ironomycin, a promising lysosomal iron-targeting small molecule, inhibited DLBCL cell proliferation at nanomolar concentrations compared with typical iron chelators. Ironomycin also induced significant cell growth inhibition, ferroptosis, and autophagy. Ironomycin treatment resulted in accumulation of DNA double-strand breaks, delayed progression of replication forks, and increased RPA2 phosphorylation, a marker of replication stress. Ironomycin significantly reduced the median number of viable primary DLBCL cells of patients without major toxicity for nontumor cells from the microenvironment and presented low toxicity in hematopoietic progenitors compared with conventional treatments. Significant synergistic effects were also observed by combining ironomycin with doxorubicin, BH3 mimetics, BTK inhibitors, or Syk inhibitors. Altogether, these data demonstrate that a subgroup of high-risk patients with DLBCL can be identified with the IS that can potentially benefit from targeting iron homeostasis. SIGNIFICANCE: Iron homeostasis represents a potential therapeutic target for high-risk patients with DLBCL that can be targeted with ironomycin to induce cell death and to sensitize tumor cells to conventional treatments. American Association for Cancer Research 2022-03-15 2022-03-15 /pmc/articles/PMC9359736/ /pubmed/35078814 http://dx.doi.org/10.1158/0008-5472.CAN-21-0218 Text en ©2022 The Authors; Published by the American Association for Cancer Research https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) license. |
spellingShingle | Metabolism and Chemical Biology Devin, Julie Cañeque, Tatiana Lin, Yea-Lih Mondoulet, Lucie Veyrune, Jean-Luc Abouladze, Matthieu Garcia De Paco, Elvira Karmous Gadacha, Ouissem Cartron, Guillaume Pasero, Philippe Bret, Caroline Rodriguez, Raphaël Moreaux, Jerome Targeting Cellular Iron Homeostasis with Ironomycin in Diffuse Large B-cell Lymphoma |
title | Targeting Cellular Iron Homeostasis with Ironomycin in Diffuse Large B-cell Lymphoma |
title_full | Targeting Cellular Iron Homeostasis with Ironomycin in Diffuse Large B-cell Lymphoma |
title_fullStr | Targeting Cellular Iron Homeostasis with Ironomycin in Diffuse Large B-cell Lymphoma |
title_full_unstemmed | Targeting Cellular Iron Homeostasis with Ironomycin in Diffuse Large B-cell Lymphoma |
title_short | Targeting Cellular Iron Homeostasis with Ironomycin in Diffuse Large B-cell Lymphoma |
title_sort | targeting cellular iron homeostasis with ironomycin in diffuse large b-cell lymphoma |
topic | Metabolism and Chemical Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9359736/ https://www.ncbi.nlm.nih.gov/pubmed/35078814 http://dx.doi.org/10.1158/0008-5472.CAN-21-0218 |
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