Proteasomal Dysfunction in Cancer: Mechanistic Pathways and Targeted Therapies

被引:0
|
作者
Bagde, Pranit Hemant [1 ]
Kandpal, Meenakshi [1 ]
Rani, Annu [1 ]
Kumar, Sachin [2 ]
Mishra, Amit [3 ]
Jha, Hem Chandra [1 ]
机构
[1] Indian Inst Technol, Dept Biosci & Biomed Engn, Infect Bioengn Grp, Indore, Madhya Pradesh, India
[2] Swami Rama Himalayan Univ, Himalayan Sch Biosci, Dehra Dun, Uttarakhand, India
[3] Indian Inst Technol, Cellular & Mol Neurobiol Unit, Jodhpur, Rajasthan, India
关键词
cancer cells; E3 ubiquitin ligase; inhibitors; pathogens; proliferation; therapy; ubiquitin-proteasome system; E3 UBIQUITIN LIGASES; F-BOX PROTEINS; NF-KAPPA-B; TUMOR-SUPPRESSOR; MULTIPLE-MYELOMA; BREAST-CANCER; IN-VIVO; MAMMALIAN PROTEASOME; PRECLINICAL MODELS; PROGNOSTIC IMPACT;
D O I
10.1002/jcb.70000
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
Proteasomes are the catalytic complexes in eukaryotic cells that decide the fate of proteins involved in various cellular processes in an energy-dependent manner. The proteasomal system performs its function by selectively destroying the proteins labelled with the small protein ubiquitin. Dysfunctional proteasomal activity is allegedly involved in various clinical disorders such as cancer, neurodegenerative disorders, ageing, and so forth, making it an important therapeutic target. Notably, compared to healthy cells, cancer cells have a higher protein homeostasis requirement and a faster protein turnover rate. The ubiquitin-proteasome system (UPS) helps cancer cells increase rapidly and experience less apoptotic cell death. Therefore, understanding UPS is essential to design and discover some effective inhibitors for cancer therapy. Hereby, we have focused on the role of the 26S proteasome complex, mainly the UPS, in carcinogenesis and seeking potential therapeutic targets in treating numerous cancers.
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页数:22
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