PAX3-FOXO1 Drives Targetable Cell State–Dependent Metabolic Vulnerabilities in Rhabdomyosarcoma

PAX3-FOXO1+ rhabdomyosarcoma cells and tumors exhibit increased sensitivity to DHFR inhibition via methotrexate, identifying a potential therapeutic vulnerability that can be exploited to treat this aggressive pediatric sarcoma.

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Publication Details

Journal
Cancer Research
Published
2025-09-05
DOI
https://doi.org/10.1158/0008-5472.can-25-0315
Primary Topic
FOXO transcription factor regulation
Type
article
Field-Weighted Citation Impact
0.00
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PAX3-FOXO1 Drives Targetable Cell State–Dependent Metabolic Vulnerabilities in Rhabdomyosarcoma

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PAX3-FOXO1 Drives Targetable Cell State–Dependent Metabolic Vulnerabilities in Rhabdomyosarcoma

Lydia W.S. Finley, Kristina Guillan, Abigail Xie, Armaan Siddiquee, Benjamin T. Jackson, Joshua D. Rabinowitz, Sangita Chakraborty, Andrew L. Kung, Filemon S. Dela Cruz, Angela M. Montero, Julia S. Brunner, Daoqi You, Katrina I. Paras, Jacob A. Boyer, Lourdes Pajuelo Torres
article en

Abstract

PAX3-FOXO1+ rhabdomyosarcoma cells and tumors exhibit increased sensitivity to DHFR inhibition via methotrexate, identifying a potential therapeutic vulnerability that can be exploited to treat this aggressive pediatric sarcoma.

Cancer ResearchVol. 85(23)
Memorial Sloan Kettering Cancer Center (US), Duke University (US), Princeton University (US), Cornell University (US)
Openalex Percentile: Top 79%
FOXO transcription factor regulation
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