Avoidance of pyroptosis accounts for the relatively high metastatic potential observed in early hybrid EMT states

EMT converts epithelial (E) phenotypes to invasive mesenchymal (M) states. However, analyses of circulating tumor cells (CTCs) indicated that biphenotypic (E+M) CTCs better correlate with metastasis. Similarly, investigations of murine tumors undergoing EMT concluded that early E+M states posses the...

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Published inbioRxiv
Main Authors Verma, Aakanksha, Genna, Alessandro, Vinik, Yaron, Nataraj, Nishant Belugali, Abedrabbo, Maha, Selvadurai, Boobash Raj, Bhandari, Tithi, Aharoni, Noa, Palaniappan Ramesh, Boguslavski, Boris, Drago, Diana, Tomer Meir Salame, Prior, Amir, Levin, Yishai, Weizman, Evitar, Zhu, Rong, Caldas, Carlos, Rueda, Oscar M, Lev, Sima, Yarden, Yosef
Format Paper
LanguageEnglish
Published Cold Spring Harbor Cold Spring Harbor Laboratory Press 27.01.2025
Cold Spring Harbor Laboratory
Edition1.1
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ISSN2692-8205
2692-8205
DOI10.1101/2025.01.26.634904

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Summary:EMT converts epithelial (E) phenotypes to invasive mesenchymal (M) states. However, analyses of circulating tumor cells (CTCs) indicated that biphenotypic (E+M) CTCs better correlate with metastasis. Similarly, investigations of murine tumors undergoing EMT concluded that early E+M states posses the highest metastatic potential. To explore this, we selected in animals with breast cancer CTCs having progressively increasing intravasation abilities. This revealed that downregulation of arrestin Arrdc4 associates with CTC aggressiveness. In xenografts, depleting Arrdc4 accelerated tumor progression, whereas overexpression hindered progression in immunocompetent, but not in immunocompromised mice. Mechanistically, high Arrdc44 suppresses glucose uptake and enhances gasdermin E, triggering pyroptosis a type of pro-inflammatory cell death. Consistently, Arrdc4's lowest levels characterize the most metastatic biphenotypic states. In patients, both epigenetic and chromosomal aberrations downregulate ARRDC4 and predict poor prognosis. In summary, the uncovered mechanism portrays pyroptosis of biphenotypic EMT cells as a rheostat of CTCs, which may resolve the controversy on the role played by EMT in metastasis.Competing Interest StatementThe authors have declared no competing interest.Footnotes* https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE280819* https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE277374
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Competing Interest Statement: The authors have declared no competing interest.
ISSN:2692-8205
2692-8205
DOI:10.1101/2025.01.26.634904