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TIM-3 Inhibitor Development: Overcoming Immune Evasion in Cancer Therapy.

Journal of medicinal chemistry 2025 Vol.68(24) p. 25754-25771

Wang L, Shen H, Jiang B, Wang X, Yang P, Sun C

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Although immune checkpoint blockade therapies targeting PD-1/PD-L1 and CTLA-4 have achieved remarkable clinical success, limitations such as low response rates and acquired resistance remain significa

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APA Wang L, Shen H, et al. (2025). TIM-3 Inhibitor Development: Overcoming Immune Evasion in Cancer Therapy.. Journal of medicinal chemistry, 68(24), 25754-25771. https://doi.org/10.1021/acs.jmedchem.5c02693
MLA Wang L, et al.. "TIM-3 Inhibitor Development: Overcoming Immune Evasion in Cancer Therapy.." Journal of medicinal chemistry, vol. 68, no. 24, 2025, pp. 25754-25771.
PMID 41363665

Abstract

Although immune checkpoint blockade therapies targeting PD-1/PD-L1 and CTLA-4 have achieved remarkable clinical success, limitations such as low response rates and acquired resistance remain significant challenges. TIM-3 has recently emerged as a key immunosuppressive receptor and a promising therapeutic target for augmenting antitumor immunity. However, the development of TIM-3 inhibitors is highly imbalanced: multiple antibody-based candidates have entered Phase III trials, whereas small-molecule inhibitors are still in the preclinical stage, with current research remaining fragmented and lacking systematic structure-activity relationship studies. This Account systematically summarizes the structural and functional mechanisms of TIM-3, with a focus on recent advances in the discovery and development of small-molecule TIM-3 inhibitors. We highlight representative lead compounds identified through virtual screening and rational design and discuss future directions to facilitate the development of novel TIM-3-targeted agents.

MeSH Terms

Humans; Hepatitis A Virus Cellular Receptor 2; Neoplasms; Animals; Antineoplastic Agents; Structure-Activity Relationship; Immune Checkpoint Inhibitors

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