Development and Therapeutic Potential of NUAKs Inhibitors
- Authors
- Faisal, Muhammad; Kim, Jae Ho; Yoo, Kyung Ho; Roh, Eun Joo; Hong, Soon Sun; Lee, So Ha
- Issue Date
- 2021-01-14
- Publisher
- AMER CHEMICAL SOC
- Citation
- JOURNAL OF MEDICINAL CHEMISTRY, v.64, no.1, pp.2 - 25
- Abstract
- NUAK isoforms, NUAK1 (ARK5) and NUAK2 (SNARK), are important members of the AMPK family of protein kinases. They are involved in a broad spectrum of physiological and cellular events, and sometimes their biological roles overlap. NUAK isoform dysregulation is associated with numerous pathological disorders, including neurodegeneration, metastatic cancer, and diabetes. Therefore, they are promising therapeutic targets in metabolic diseases and cancers; consequently, various NUAK-targeted inhibitors have been disclosed. The first part of this review comprises a brief discussion of the homology, expression, structure, and characteristics of NUAK isoforms. The second part focuses on NUAK isoforms' involvement in crucial biological operations, including mechanistic findings, highlighting how their abnormal functioning contributes to disease progression and quality of life. The third part summarizes the key findings and applications of targeting NUAK isoforms for treating multiple cancers and neurodegenerative disorders. The final part systematically presents a critical review and analysis of the literature on NUAK isoform inhibitions through small molecules.
- Keywords
- VENTRAL BODY-WALL; EPITHELIAL-MESENCHYMAL TRANSITION; LIGHT-CHAIN PHOSPHORYLATION; AMPK-MEDIATED REGULATION; KINASE INHIBITOR; PROTEIN-KINASE; GLUCOSE-TRANSPORT; TARGETING NUAK1; SUPPRESSES INVASION; MYOSIN PHOSPHATASE; VENTRAL BODY-WALL; EPITHELIAL-MESENCHYMAL TRANSITION; LIGHT-CHAIN PHOSPHORYLATION; AMPK-MEDIATED REGULATION; KINASE INHIBITOR; PROTEIN-KINASE; GLUCOSE-TRANSPORT; TARGETING NUAK1; SUPPRESSES INVASION; MYOSIN PHOSPHATASE; NUAK1; NUAK2; ARK5; SNARK; Cancer; Inhibitors
- ISSN
- 0022-2623
- URI
- https://pubs.kist.re.kr/handle/201004/117528
- DOI
- 10.1021/acs.jmedchem.0c00533
- Appears in Collections:
- KIST Article > 2021
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