Mitochondrial division inhibitor (mdivi-1) induces extracellular matrix (ECM)-detachment of viable breast cancer cells by a DRP1-independent mechanism
| dc.coverage | DOI: 10.1038/s41598-024-64228-9 | |
| dc.creator | Silva-Pavez, Eduardo | |
| dc.creator | Mendoza, Elizabeth | |
| dc.creator | Morgado-Cáceres, Pablo | |
| dc.creator | Ahumada-Castro, Ulises | |
| dc.creator | Bustos, Galdo | |
| dc.creator | Kangme-Encalada, Matías | |
| dc.creator | de Arbina, Amaia Lopez | |
| dc.creator | Puebla-Huerta, Andrea | |
| dc.creator | Muñoz, Felipe | |
| dc.creator | Cereceda, Lucas | |
| dc.creator | Varas-Godoy, Manuel | |
| dc.creator | Hidalgo, Yessia | |
| dc.creator | Cardenas, J. Cesar | |
| dc.date | 2024 | |
| dc.date.accessioned | 2025-11-18T19:45:11Z | |
| dc.date.available | 2025-11-18T19:45:11Z | |
| dc.description | <p>Increasing evidence supports the hypothesis that cancer progression is under mitochondrial control. Mitochondrial fission plays a pivotal role in the maintenance of cancer cell homeostasis. The inhibition of DRP1, the main regulator of mitochondrial fission, with the mitochondrial division inhibitor (mdivi-1) had been associated with cancer cell sensitivity to chemotherapeutics and decrease proliferation. Here, using breast cancer cells we find that mdivi-1 induces the detachment of the cells, leading to a bulk of floating cells that conserved their viability. Despite a decrease in their proliferative and clonogenic capabilities, these floating cells maintain the capacity to re-adhere upon re-seeding and retain their migratory and invasive potential. Interestingly, the cell detachment induced by mdivi-1 is independent of DRP1 but relies on inhibition of mitochondrial complex I. Furthermore, mdivi-1 induces cell detachment rely on glucose and the pentose phosphate pathway. Our data evidence a novel DRP1-independent effect of mdivi-1 in the attachment of cancer cells. The generation of floating viable cells restricts the use of mdivi-1 as a therapeutic agent and demonstrates that mdivi-1 effect on cancer cells are more complex than anticipated.</p> | eng |
| dc.identifier | https://investigadores.uandes.cl/en/publications/d93e1fce-78d0-41b1-9f87-b71b0eaddcc1 | |
| dc.identifier.uri | https://repositorio.uandes.cl/handle/uandes/53836 | |
| dc.language | eng | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.source | vol.14 (2024) nr.1 | |
| dc.subject | Cancer | |
| dc.subject | Cell detachment | |
| dc.subject | Mdivi-1 | |
| dc.subject | Metabolism | |
| dc.subject | Mitochondrial complex I | |
| dc.subject | SDG 3 - Good Health and Well-being | |
| dc.title | Mitochondrial division inhibitor (mdivi-1) induces extracellular matrix (ECM)-detachment of viable breast cancer cells by a DRP1-independent mechanism | eng |
| dc.type | Article | eng |
| dc.type | Artículo | spa |