CRBN-PROTACs in Cancer Therapy: From Mechanistic Insights to Clinical Applications

被引:0
|
作者
Thapa, Riya [1 ]
Bhat, Asif Ahmad [1 ]
Gupta, Gaurav [2 ,3 ]
Renuka Jyothi, S. [4 ]
Kaur, Irwanjot [5 ]
Kumar, Sachin [6 ]
Sharma, Naveen [7 ]
Prasad, G. V. Siva [8 ]
Pramanik, Atreyi [9 ]
Ali, Haider [10 ,11 ]
机构
[1] Uttaranchal Univ, Uttaranchal Inst Pharmaceut Sci, Dehra Dun, India
[2] Chitkara Univ, Chitkara Coll Pharm, Ctr Res Impact & Outcome, Rajpura, Punjab, India
[3] Ajman Univ, Ctr Med & Bioallied Hlth Sci Res, Ajman, U Arab Emirates
[4] JAIN Univ, Sch Sci, Dept Biotechnol & Genet, Bangalore, Karnataka, India
[5] Vivekananda Global Univ, Dept Allied Healthcare & Sci, Jaipur, Rajasthan, India
[6] NIMS Univ Rajasthan, NIMS Inst Pharm, Jaipur, India
[7] Chandigarh Pharm Coll, Chandigarh Grp Coll, Mohali, Punjab, India
[8] Raghu Engn Coll, Dept Chem, Visakhapatnam, Andhra Pradesh, India
[9] Uttaranchal Univ, Sch Appl & Life Sci, Div Res & Innovat, Dehra Dun, India
[10] Saveetha Univ, Saveetha Inst Med & Tech Sci, Saveetha Med Coll, Ctr Global Hlth Res, Chennai, India
[11] Kyrgyz State Med Coll, Dept Pharmacol, Bishkek, Kyrgyzstan
关键词
cancer therapy; Cereblon; CRBN; drug resistance; E3 ubiquitin ligase; PROTACs; solid tumors; targeted protein degradation; the ubiquitin-proteasome system; TARGETED PROTEIN-DEGRADATION; SELECTIVE DEGRADATION; UBIQUITIN LIGASE; CEREBLON EXPRESSION; CHIMERAS PROTACS; DRUG DISCOVERY; LUNG-CANCER; PATHWAYS; EPIDEMIOLOGY; MANAGEMENT;
D O I
10.1111/cbdd.70009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cereblon (CRBN), a member of the E3 ubiquitin ligase complex, has gained significant attention as a therapeutic target in cancer. CRBN regulates the degradation of various proteins in cancer progression, including transcription factors and signaling molecules. PROTACs (proteolysis-targeting chimeras) are a novel approach that uses the cell's degradation system to remove disease-causing proteins selectively. CRBN-dependent PROTACs work by tagging harmful proteins for destruction through the ubiquitin-proteasome system. This strategy offers several advantages over traditional protein inhibition methods, including the potential to overcome drug resistance. Recent progress in developing CRBN-based PROTACs has shown promising preclinical results in both hematologic malignancies and solid tumors. Additionally, CRBN-based PROTACs have enhanced our understanding of CRBN's role in cancer, potentially serving as biomarkers for patient stratification and predicting therapeutic responses. In this review, we delineate the mechanisms of action for CRBN-dependent PROTACs (CRBN-PROTACs), summarize recent advances in preclinical and clinical applications, and provide our perspective on future development.
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页数:22
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