mTORC1 shutdown unleashes TFEB to drive triple-negative breast cancer invasion
Dev Cell. 2025 Apr 7;60(7):979-981. doi: 10.1016/j.devcel.2025.03.006.
Published on April 8, 2025
ABSTRACT
The PI3K/AKT/mTOR pathway is considered a key therapeutic target in triple-negative breast cancer (TNBC). In this issue of Developmental Cell, Remy et al. challenge this idea by demonstrating that mTORC1 inhibition activates TFEB, promoting MT1-MMP exocytosis, ECM degradation, and increased cell invasion, especially when combined with chemotherapy.
PMID:40199239 | DOI:10.1016/j.devcel.2025.03.006
Latest Publications
- Staphylococcus aureus Augments Epithelial Skin Barrier Damage Through T Cell Activation in Cutaneous T Cell Lymphoma
- XMD8-92 and JWG-045 exhibit anti-ferroptotic activities, independently of inhibiting ERK5
- Molecular Characterization of Extracellular Vesicles From Human B Cell Lymphomas: Methodological Comparison to Vesicles From Patient Serum
- Evolving epigenomics of immune cells at single-nucleus resolution in children en route to type 1 diabetes
- Restoring the tumour mechanophenotype of vocal fold cancer reverts its malignant properties