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These receptors bind to testosterone and use the hormone to fuel tumor growth

Conclusions This review provides insights into the influence of DPP-4 on bone metabolism and delineates the potential mechanisms of the interaction between DPP-4 and bone (Fig

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Furthermore, developing small molecule inhibitors targeting BCAA transporters in tumor cells and immunosuppressive cells allows CD8 + T cells to obtain amino acid metabolic advantages in the immune microenvironment and enhance the anti-tumor effect

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