Inhibition of Tumor Microenvironment-Driven JAK-STAT Signaling Enhances Response to Arginine Deprivation Therapy in Triple-Negative Breast Cancer

Argininosuccinate synthetase 1 (ASS1) expression and arginine availability are key metabolic determinants that influence tumor fitness and regulate immune interactions within the tumor microenvironment (TME). Using an orthotopic triple-negative breast cancer (TNBC) model, we demonstrate that arginine deprivation heightens tumor dependence on the TME for survival. Mechanistically, fibroblasts sustain tumor viability by supplying arginine, whereas macrophages cooperate with stromal cues to activate Janus kinase-signal transducer and activator of transcription (JAK-STAT) signaling, thereby enhancing tumor survival. Concordantly, a JAK-STAT gene-expression signature correlates with ASS1 levels in human TNBC datasets. Translationally, combined pharmacological inhibition of JAK signaling with arginine deprivation markedly suppresses tumor growth. Together, these findings reveal a TME-driven, targetable stromal-immune circuit that enables tumors to withstand arginine deficiency-induced metabolic stress. Broadly, our work highlights that mapping and strategically inducing metabolic dependencies can reveal actionable compensatory pathways, offering opportunities to improve cancer therapy.

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Publication Details

Journal
Cells
Published
2025-12-23
DOI
https://doi.org/10.3390/cells15010025
Primary Topic
Cancer Research and Treatments
Type
article
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article

Inhibition of Tumor Microenvironment-Driven JAK-STAT Signaling Enhances Response to Arginine Deprivation Therapy in Triple-Negative Breast Cancer

Roni Oren, Tevie Mehlman, Bareket Dassa, Ron Rotkopf et al.
Cells
Cancer Research and Treatments
article

Inhibition of Tumor Microenvironment-Driven JAK-STAT Signaling Enhances Response to Arginine Deprivation Therapy in Triple-Negative Breast Cancer

Roni Oren, Tevie Mehlman, Bareket Dassa, Ron Rotkopf, Alexander Brandis, Michal Levi, Elizabeta Bab-Dinitz, Nataly Rosenfeld, Saar Ezagouri, Ayelet Erez, Mirie Zerbib, Sara Donzelli, Yarden Ariav, Nitsan Nimni, Giovanni Blandino, Naama Darzi, Neel Sanghvi, Lital N. Adler, Yuri Kuznetsov, Shahar Ziman, R Seger, Hila Tishler, Kuoyuan Cheng, Eytan Ruppin, Kun Wang, Gil Stelzer, Omer Goldman, Hillary Maniriho, Sivan Galai
article en

Abstract

Argininosuccinate synthetase 1 (ASS1) expression and arginine availability are key metabolic determinants that influence tumor fitness and regulate immune interactions within the tumor microenvironment (TME). Using an orthotopic triple-negative breast cancer (TNBC) model, we demonstrate that arginine deprivation heightens tumor dependence on the TME for survival. Mechanistically, fibroblasts sustain tumor viability by supplying arginine, whereas macrophages cooperate with stromal cues to activate Janus kinase-signal transducer and activator of transcription (JAK-STAT) signaling, thereby enhancing tumor survival. Concordantly, a JAK-STAT gene-expression signature correlates with ASS1 levels in human TNBC datasets. Translationally, combined pharmacological inhibition of JAK signaling with arginine deprivation markedly suppresses tumor growth. Together, these findings reveal a TME-driven, targetable stromal-immune circuit that enables tumors to withstand arginine deficiency-induced metabolic stress. Broadly, our work highlights that mapping and strategically inducing metabolic dependencies can reveal actionable compensatory pathways, offering opportunities to improve cancer therapy.

CellsVol. 15(1)
University of Illinois Urbana-Champaign (US), Rabin Medical Center (IL), National Cancer Institute (US), Istituti di Ricovero e Cura a Carattere Scientifico (IT), Weizmann Institute of Science (IL)
Openalex Percentile: Top 32%
Cancer Research and Treatments
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