Authors
Josep Tarragó-Celada, Asad S Mahmood, Yulia Panina, Sakshi Lalwani, Samantha Atkinson, Amy Spicer, Michael Kossifos, Weigang Cai, Ersa Gjelaj, Sharavan Vishaan Venkateswaran, Saidu Sesay, Izadora Furlani, Nathalie Michelle Legrave, Tegan Gilmore, Richard Mitter, Jayanta Bordoloi, Avinash Ghanate, Vincen Wu, Zoltán Takáts, Bin Yan, Alex Dexter, Rory T Steven, Josephine Bunch, George Georgiou, Everett M Stone, Míriam Tarrado-Castellarnau, James I MacRae, Richard J Burt, Mariia Yuneva
Published in
Cancer research. Jul 07, 2026. Epub Jul 07, 2026.
Abstract
Metastatic disease remains a major cause of cancer-related mortality. Recent studies suggest that dissemination to other organs comes with metabolic changes that allow the metastasizing cancer cells to adapt to new microenvironments. A deeper knowledge of these specific metabolic features and associated vulnerabilities could lead to the development of more effective therapies against metastasis. We used in vivo and ex vivo models of MYC-driven breast tumorigenesis to explore the key metabolic pathways that change when mammary gland tumor cells metastasize to the lung. Stable isotope-resolved metabolomics, mass spectrometry imaging, and single-cell RNA sequencing demonstrated that mammary gland tumor-derived lung metastases have increased synthesis of glutathione fueled by increased cystine uptake. Metastatic cells relied heavily on the availability of extracellular cysteine or cystine, possibly due to downregulated intracellular cysteine synthesis through the transsulfuration pathway. When combined with focal radiotherapy, the amino acid degrader cyst(e)inase effectively reduced metastatic burden in the lungs. Together, these findings show that targeting cystine/cysteine exploits a metabolic dependency that is unique to metastatic cells and acts as a sensitizer to radiotherapy-induced oxidative stress, offering a promising targeted strategy.
PMID:
42412619
Bibliographic data and abstract were imported from PubMed on 08 Jul 2026.
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