4.6 Review

USP7 Inhibitors in Cancer Immunotherapy: Current Status and Perspective

Journal

CANCERS
Volume 14, Issue 22, Pages -

Publisher

MDPI
DOI: 10.3390/cancers14225539

Keywords

ubiquitin-specific protease 7; cancer; immunotherapy; small-molecule inhibitors

Categories

Funding

  1. Sirius University of Science and Technology [BTH-RND-2128]

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Elevated levels of USP7 are associated with poor survival in many cancers. Inhibition of USP7 can affect the function of regulatory T cells and tumor-associated macrophages, as well as decrease levels of oncogenic markers. The application of USP7 inhibitors, alone or in combination with immunotherapy, has great potential for cancer treatment.
Simple Summary Elevated levels of ubiquitin-specific protease 7 (USP7) are associated with poor survival in many cancers. This protein impairs the balance of various cellular proteins and regulates the anti-tumor immune response. Its inhibition affects regulatory T cells and tumor-associated macrophages and decreases levels of various oncogenic markers. Thus, the application of USP7 inhibitors alone and in combination with cancer immunotherapeutics is highly promising. We review the potential benefits of the application of USP7 inhibitors for cancer immunotherapy and their interplay with other cancer therapeutics. Ubiquitin-specific protease 7 (USP7) regulates the stability of a plethora of intracellular proteins involved in the suppression of anti-tumor immune responses and its overexpression is associated with poor survival in many cancers. USP7 impairs the balance of the p53/MDM2 axis resulting in the proteasomal degradation of the p53 tumor suppressor, a process that can be reversed by small-molecule inhibitors of USP7. USP7 was shown to regulate the anti-tumor immune responses in several cases. Its inhibition impedes the function of regulatory T cells, promotes polarization of tumor-associated macrophages, and reduces programmed death-ligand 1 (PD-L1) expression in tumor cells. The efficacy of small-molecule USP7 inhibitors was demonstrated in vivo. The synergistic effect of combining USP7 inhibition with cancer immunotherapy is a promising therapeutic approach, though its clinical efficacy is yet to be proven. In this review, we focus on the recent developments in understanding the intrinsic role of USP7, its interplay with other molecular pathways, and the therapeutic potential of targeting USP7 functions.

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