Abstract
Topoisomerase IIα has been a representative anti-cancer target for decades thanks to its functional necessity in highly prolifera-tive cancer cells. As type of topoisomerase IIα targeting drugs, topoisomerase II poisons are frequently in clinical usage. However, topoisomerase II poisons result in crucial consequences resulted from mechanistically induced DNA toxicity. For this reason, it is needed to develop catalytic inhibitors of topoisomerase IIα through the alternative mechanism of enzymatic regulation. As a catalytic inhibitor of topoisomerase IIα, AK-I-191 was previously reported for its enzyme inhibitory activity. In this study, we clarified the mechanism of AK-I-191 and conducted various types of spectroscopic and biological evaluations for deeper understanding of its mechanism of action. Conclusively, AK-I-191 represented potent topoisomerase IIα inhibitory activity through binding to minor groove of DNA double helix and showed synergistic effects with tamoxifen in antiproliferative activity.
Original language | English |
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Pages (from-to) | 562-570 |
Number of pages | 9 |
Journal | Biomolecules and Therapeutics |
Volume | 29 |
Issue number | 5 |
DOIs | |
State | Published - Sep 2021 |
Bibliographical note
Publisher Copyright:© 2021 The Korean Society of Applied Pharmacology.
Keywords
- 2-b]-pyridinol derivative
- 4-diphenyl Indeno[1
- DNA minor groove binder
- Halogenated 2
- Topoisomerase IIα
- Topoisomerase catalytic inhibitor
- Trifluoromethyl 2-(3-trifluoromethylphenyl)-4-(3-h