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Inhibiting SCD expression by IGF1R during lorlatinib therapy sensitizes melanoma to ferroptosis
Induction of ferroptosis is an emerging strategy to suppress melanoma progression. Strategies to enhance the sensitivity to ferroptosis induction would be a major advance in melanoma therapy. Here, we used a drug synergy screen that combined a ferroptosis inducer, RSL3, with 240 anti-tumor drugs fro...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10009726/ https://www.ncbi.nlm.nih.gov/pubmed/36889082 http://dx.doi.org/10.1016/j.redox.2023.102653 |
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author | Zeng, Furong Ye, Lin Zhou, Qian He, Yi Zhang, Yilei Deng, Guangtong Chen, Xiang Liu, Hong |
author_facet | Zeng, Furong Ye, Lin Zhou, Qian He, Yi Zhang, Yilei Deng, Guangtong Chen, Xiang Liu, Hong |
author_sort | Zeng, Furong |
collection | PubMed |
description | Induction of ferroptosis is an emerging strategy to suppress melanoma progression. Strategies to enhance the sensitivity to ferroptosis induction would be a major advance in melanoma therapy. Here, we used a drug synergy screen that combined a ferroptosis inducer, RSL3, with 240 anti-tumor drugs from the FDA-approved drug library and identified lorlatinib to synergize with RSL3 in melanoma cells. We further demonstrated that lorlatinib sensitized melanoma to ferroptosis through inhibiting PI3K/AKT/mTOR signaling axis and its downstream SCD expression. Moreover, we found that lorlatinib's target IGF1R, but not ALK or ROS1, was the major mediator of lorlatinib-mediated sensitivity to ferroptosis through targeting PI3K/AKT/mTOR signaling axis. Finally, lorlatinib treatment sensitized melanoma to GPX4 inhibition in preclinical animal models, and melanoma patients with low GPX4 and IGF1R expression in their tumors survived for longer period. Altogether, lorlatinib sensitizes melanoma to ferroptosis by targeting IGF1R-mediated PI3K/AKT/mTOR signaling axis, suggesting that combination with lorlatinib could greatly expand the utility of GPX4 inhibition to melanoma patients with IGF1R-proficient expression. |
format | Online Article Text |
id | pubmed-10009726 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-100097262023-03-14 Inhibiting SCD expression by IGF1R during lorlatinib therapy sensitizes melanoma to ferroptosis Zeng, Furong Ye, Lin Zhou, Qian He, Yi Zhang, Yilei Deng, Guangtong Chen, Xiang Liu, Hong Redox Biol Research Paper Induction of ferroptosis is an emerging strategy to suppress melanoma progression. Strategies to enhance the sensitivity to ferroptosis induction would be a major advance in melanoma therapy. Here, we used a drug synergy screen that combined a ferroptosis inducer, RSL3, with 240 anti-tumor drugs from the FDA-approved drug library and identified lorlatinib to synergize with RSL3 in melanoma cells. We further demonstrated that lorlatinib sensitized melanoma to ferroptosis through inhibiting PI3K/AKT/mTOR signaling axis and its downstream SCD expression. Moreover, we found that lorlatinib's target IGF1R, but not ALK or ROS1, was the major mediator of lorlatinib-mediated sensitivity to ferroptosis through targeting PI3K/AKT/mTOR signaling axis. Finally, lorlatinib treatment sensitized melanoma to GPX4 inhibition in preclinical animal models, and melanoma patients with low GPX4 and IGF1R expression in their tumors survived for longer period. Altogether, lorlatinib sensitizes melanoma to ferroptosis by targeting IGF1R-mediated PI3K/AKT/mTOR signaling axis, suggesting that combination with lorlatinib could greatly expand the utility of GPX4 inhibition to melanoma patients with IGF1R-proficient expression. Elsevier 2023-03-01 /pmc/articles/PMC10009726/ /pubmed/36889082 http://dx.doi.org/10.1016/j.redox.2023.102653 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Paper Zeng, Furong Ye, Lin Zhou, Qian He, Yi Zhang, Yilei Deng, Guangtong Chen, Xiang Liu, Hong Inhibiting SCD expression by IGF1R during lorlatinib therapy sensitizes melanoma to ferroptosis |
title | Inhibiting SCD expression by IGF1R during lorlatinib therapy sensitizes melanoma to ferroptosis |
title_full | Inhibiting SCD expression by IGF1R during lorlatinib therapy sensitizes melanoma to ferroptosis |
title_fullStr | Inhibiting SCD expression by IGF1R during lorlatinib therapy sensitizes melanoma to ferroptosis |
title_full_unstemmed | Inhibiting SCD expression by IGF1R during lorlatinib therapy sensitizes melanoma to ferroptosis |
title_short | Inhibiting SCD expression by IGF1R during lorlatinib therapy sensitizes melanoma to ferroptosis |
title_sort | inhibiting scd expression by igf1r during lorlatinib therapy sensitizes melanoma to ferroptosis |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10009726/ https://www.ncbi.nlm.nih.gov/pubmed/36889082 http://dx.doi.org/10.1016/j.redox.2023.102653 |
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