Rising Star in Immunotherapy: Development and Therapeutic Potential of Small-Molecule Inhibitors Targeting Casitas B Cell Lymphoma-b (Cbl-b).
Lixin ZhouJiamei YangKuojun ZhangTianyu WangSheng JiangXiangyu ZhangPublished in: Journal of medicinal chemistry (2024)
Casitas B cell lymphoma-b (Cbl-b) is a vital negative regulator of TCR and BCR signaling pathways, playing a significant role in setting an appropriate threshold for the activation of T cells and controlling the tolerance of peripheral T cells via a variety of mechanisms. Overexpression of Cbl-b leads to immune hyporesponsiveness of T cells. Conversely, the deficiency of Cbl-b in T cells results in markedly increased production of IL-2, even in the lack of CD28 costimulation in vitro. And Cbl-b -/- mice spontaneously reject multifarious cancers. Therefore, Cbl-b may be associated with immune-mediated diseases, and blocking Cbl-b could be considered as a new antitumor immunotherapy strategy. In this review, the possible regulatory mechanisms and biological potential of Cbl-b for antitumor immunotherapy are summarized. Besides, the potential roles of Cbl-b in immune-mediated diseases are comprehensively discussed, with emphasis on Cbl-b immune-oncology agents in the preclinical stage and clinical trials.
Keyphrases
- small molecule
- clinical trial
- signaling pathway
- diffuse large b cell lymphoma
- acute lymphoblastic leukemia
- risk assessment
- stem cells
- type diabetes
- oxidative stress
- randomized controlled trial
- palliative care
- epithelial mesenchymal transition
- metabolic syndrome
- bone marrow
- skeletal muscle
- human health
- young adults
- cell therapy
- endoplasmic reticulum stress
- nk cells