Publication | Open Access
Ammonium tetrathiomolybdate enhances the antitumor effects of cetuximab via the suppression of osteoclastogenesis in head and neck squamous carcinoma
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Citations
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References
2018
Year
Bone InvasionHnscc CellsAmmonium TetrathiomolybdateNeck Squamous CarcinomaRedox BiologyOsteoporosisTumor BiologyOxidative StressBone Morphogenic ProteinCancer Cell BiologyRadiopharmaceutical TherapyAnti-cancer AgentRadiation OncologyBiological Inorganic ChemistryCancer ResearchBiochemistryMedicineCancer TreatmentPharmacologyCell BiologyTumor MicroenvironmentOsteocalcinBioactive MetalMetalloproteinCopper ChelatorAntitumor EffectsHead And Neck CancerOncology
Head and neck squamous cell carcinoma (HNSCC) poses a significant challenge clinically where one of the mechanisms responsible for the invasion into facial bones occurs via the activation of osteoclasts. Copper has been demonstrated to play a key role in skeletal remodeling. However, the role of copper in cancer-associated bone destruction is thus far unknown. Lysyl oxidase (LOX) is a copper-dependent enzyme that promotes osteoclastogenesis. In the present study, we investigated the effects of copper on HNSCC with bone invasion by the copper chelator, ammonium tetrathiomolybdate (TM) in vitro and in vivo. We demonstrate that TM blocks the proliferation of HNSCC cells, inhibits LOX activation and decreases the expression of the receptor activator of nuclear factor-κB ligand (RANKL) in osteoblasts and osteocytes, subsequently suppressing bone destruction. These findings suggest that copper is a potential target for the treatment of HNSCCs associated with bone destruction.
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