Affiliation:
1. Department of Chemistry, University College of Science, Saifabad, Osmania University, Hyderabad, Telangana -
500004, India
2. Molecular Modelling Research Laboratory, Department of Chemistry, Osmania University, Hyderabad,
Telangana - 500007, India
Abstract
Abstract:
Cancer is a complex disease that develops when abnormal cells divide uncontrollably as
a consequence of unregulated cell cycle protein activity. Therefore, the cell cycle is crucial for
maintaining homeostasis inside the cells during DNA replication and cell division. The presence of
mutations within specific genes can disrupt the equilibrium within cells, ultimately leading to the
growth of cancer. CDK20 (Cyclin-Dependent Kinase 20) is recently identified as a major controller
of cell cycle checkpoints, which regulate cell growth and proliferation and perform a role in
the development of many malignancies. CCRK (Cell-Cycle Related Kinase) has recently been renamed
CDK20. Emerging studies proclaimed that the upregulation of CDK20 was identified in cancers
of the ovary, brain, colon, stomach, liver, and lung. CDK20 was thought to have Cyclin-dependent
activating kinase (CAK) activity for CDK2 when it is complexed with Cyclin H. Furthermore,
recent studies revealed that CDK20 is involved in the Wnt, EZH2/NF-B, and KEAP1-NRF2 signaling
pathways, all of which are interconnected to cancer formation and proliferation. In addition, the
structure of CDK20 was predicted using ColabFold, a powerful software integrating AlphaFold's
advanced AI system. The present review focuses on a systematic overview of the current knowledge
on CDK20 derived from in vitro and in vivo studies and emphasizes its role in carcinogenesis.
The validation comparison of the existing CDK20 AlphaFold structure with the ColabFold was
found to be exceptionally fast and accurate in generating reliable models.
Publisher
Bentham Science Publishers Ltd.
Subject
Clinical Biochemistry,Drug Discovery,Pharmacology,Molecular Medicine
Cited by
2 articles.
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