FASEB BioAdvances · 2021 · 21 citations · 28 references
MedicineOncologyPharmacologyChemotherapyMolecular OncologySignal TransductionCancer Cell SignalingTargeted Cancer TherapyTargeted TherapyBasal Cell Carcinoma SignalingKinase Signaling InhibitorsProtein Kinase InhibitorsSmoothened Activation
Abstract Vismodegib, a Smoothened antagonist, is clinically approved for treatment of human basal cell carcinoma (BCC), in the clinical trials of medulloblastoma (MB) and other cancers. However, a significant proportion of these tumors fail to respond to Vismodegib after a period of treatment. Here, we find that AMPK agonists, A769662, and Metformin, can inhibit GLI1 activity and synergize with Vismodegib to suppress MB cell growth in vitro and in vivo . Furthermore, combination of AMPK agonists with Vismodegib is effective in overcoming Vismodegib‐resistant MB. This is the first report demonstrating that combining AMPK agonist (Metformin) and SHH pathway inhibitor (Vismodegib) confers synergy for MB treatment and provides an effective chemotherapeutic regimen that can be used to overcome resistance to Vismodegib in SHH‐driven cancers.
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The LKB1 tumor suppressor negatively regulates mTOR signaling
Reuben J. Shaw, Nabeel Bardeesy, Brendan D. Manning et al. · Cancer Cell · 2004 · 1.1K citations · Full text
Genome Sequencing of SHH Medulloblastoma Predicts Genotype-Related Response to Smoothened Inhibition
Marcel Kool, David Jones, Natalie Jäger et al. · Cancer Cell · 2014 · 779 citations · Full text
Life Sciences, Genetics, Oncology +14
ERK promotes tumorigenesis by inhibiting FOXO3a via MDM2-mediated degradation
Jer-Yen Yang, Cong S. Zong, Weiya Xia et al. · Nature Cell Biology · 2008 · 699 citations