Ubiquitination Enzymes in Cancer, Cancer Immune Evasion, and Potential Therapeutic Opportunities

被引:0
|
作者
Awan, Aiman B. [1 ]
Osman, Maryiam Jama Ali [1 ,2 ]
Khan, Omar M. [1 ]
机构
[1] Hamad Bin Khalifa Univ, Coll Hlth & Life Sci, POB 34110, Doha, Qatar
[2] Sidra Med, Res Branch, POB 34110, Doha, Qatar
关键词
ubiquitination; cell cycle; E3; ligases; oncogenes; tumor suppressor; PROTACs; cancer; immune evasion; SMALL-MOLECULE INHIBITORS; TUMOR-SUPPRESSOR; E3; LIGASE; ACTIVATING ENZYME; PEVONEDISTAT TAK-924/MLN4924; PROTEASOMAL DEGRADATION; MEDIATED DEGRADATION; PROTEIN-DEGRADATION; NEGATIVE REGULATION; MASTER REGULATOR;
D O I
10.3390/cells14020069
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Ubiquitination is cells' second most abundant posttranslational protein modification after phosphorylation. The ubiquitin-proteasome system (UPS) is critical in maintaining essential life processes such as cell cycle control, DNA damage repair, and apoptosis. Mutations in ubiquitination pathway genes are strongly linked to the development and spread of multiple cancers since several of the UPS family members possess oncogenic or tumor suppressor activities. This comprehensive review delves into understanding the ubiquitin code, shedding light on its role in cancer cell biology and immune evasion. Furthermore, we highlighted recent advances in the field for targeting the UPS pathway members for effective therapeutic intervention against human cancers. We also discussed the recent update on small-molecule inhibitors and PROTACs and their progress in preclinical and clinical trials.
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页数:35
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