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New Polymethoxyflavones from Evoke DNA Biosynthesis-Inhibitory Activity in An Oral Squamous Carcinoma (SCC-25) Cell Line

Overview
Journal Molecules
Publisher MDPI
Specialty Biology
Date 2022 Jul 27
PMID 35889288
Authors
Affiliations
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Abstract

Four new compounds, 5-hydroxy-2',6'-dimethoxyflavone (), 5-hydroxy-2',3',6'-trimethoxyflavone (), 5-dihydroxy-6-methoxyflavone (), and 5,6'-dihydroxy-2',3'-dimethoxyflavone (), and three known compounds, 1,3-diphenylpropane-1,3-dione (), 5-hydroxyflavone (), and 5-hydroxy-2'-methoxyflavone (), were isolated from the aerial parts of . Their chemical structures were determined through the use of spectral, spectroscopic and crystallographic methods. The quantitative analysis of the compounds () and the zapotin () in methanol (), petroleum (), and two chloroform extracts ( and ) were also determined using HPLC-PDA. The biological activity of these compounds and extracts on the oral squamous carcinoma cell (SCC-25) line was investigated by considering their cytotoxic effects using the MTT assay. Subsequently, the most active compounds and extracts were assessed for their effect on DNA biosynthesis. It was found that all tested samples during 48 h treatment of SCC-25 cells induced the DNA biosynthesis-inhibitory activity: compound (IC, 29.10 ± 1.45 µM), compound (IC, 40.60 ± 1.65 µM) and extracts (IC, 20.33 ± 1.01 µM), (IC, 14.90 ± 0.74 µg), (IC, 16.70 ± 0.83 µg), and (IC, 30.30 ± 1.15 µg). The data suggest that the novel polymethoxyflavones isolated from evoke potent DNA biosynthesis inhibitory activity that may be considered in further studies on experimental pharmacotherapy of oral squamous cell carcinoma.

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References
1.
Fridlender M, Kapulnik Y, Koltai H . Plant derived substances with anti-cancer activity: from folklore to practice. Front Plant Sci. 2015; 6:799. PMC: 4589652. DOI: 10.3389/fpls.2015.00799. View

2.
Jakimiuk K, Sari S, Milewski R, Supuran C, Sohretoglu D, Tomczyk M . Flavonoids as tyrosinase inhibitors in and models: basic framework of SAR using a statistical modelling approach. J Enzyme Inhib Med Chem. 2021; 37(1):421-430. PMC: 8735877. DOI: 10.1080/14756366.2021.2014832. View

3.
Kopustinskiene D, Jakstas V, Savickas A, Bernatoniene J . Flavonoids as Anticancer Agents. Nutrients. 2020; 12(2). PMC: 7071196. DOI: 10.3390/nu12020457. View

4.
Szoka L, Nazaruk J, Stocki M, Isidorov V . Santin and cirsimaritin from Betula pubescens and Betula pendula buds induce apoptosis in human digestive system cancer cells. J Cell Mol Med. 2021; 25(24):11085-11096. PMC: 8650031. DOI: 10.1111/jcmm.17031. View

5.
Tokalov S, Kind B, Wollenweber E, Gutzeit H . Biological effects of epicuticular flavonoids from Primula denticulata on human leukemia cells. J Agric Food Chem. 2004; 52(2):239-45. DOI: 10.1021/jf0347160. View