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As an emerging oncotherapeutic strategy, cuproptosis-directed therapy holds broad promise for OSCC, and future exploration should therefore reach beyond ionophores and nanomedicines to encompass systematic mining of natural-product libraries for plant-derived cuproptosis inducers, structure-based design of next-generation agents that selectively engage FDX1, DLAT or ATP7B, and rational integration of cuproptosis activators with radiation or cisplatin so as to override canonical resistance pathways

Wu MX, Ustyugova IV, Han L, Akilov OE