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doi: 10.1093/nar/gkae973 Summary Keywords cuproptosis, ferroptosis, nano-drug delivery systems, oral squamous cell carcinoma, programmed cell death Citation Ma X, Chen Y, Mai H, Lai P, Alimujiang A and Lu M (2026) From molecular crosstalk to precision therapy: targeting ferroptosis and cuproptosis in oral squamous cell carcinoma

168 Monocarboxylate transporters (MCTs) 1--4 are proton-dependent membrane proteins that serve as critical mediators of transmembrane flux for glycolysis-derived metabolites (i.e., lactate and pyruvate) and ketone bodies (i.e., acetoacetate and -hydroxybutyrate)

Ferroptosis inhibitors have also been shown to ameliorate HSC deficiencies in MYSM1 function loss (Zhao et al., 2023)

For instance, the anti-angiogenic drug sorafenib and the photosensitizer chlorin e6 can self-assemble into nanostructures for synergistic PTT/PDT and anti-tumor angiogenesis therapy (Wei et al