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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...

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Autores principales: Zeng, Furong, Ye, Lin, Zhou, Qian, He, Yi, Zhang, Yilei, Deng, Guangtong, Chen, Xiang, Liu, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
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.
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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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