CYTOTOXIC ACTIVITY OF 4H–CHROMENES ON COLO 205 HUMAN COLON ADENOCARCINOMA CELL LINE

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Suchada Jongrungruangchok
Nalinee Pradubyat
Thanapat Songsak
Supakit Wongwiwatthananukit

Abstract

H-chromenes are synthetic benzopyran derivatives which have various pharmacological activities. This study aimed to investigate and compare the cytotoxic activity of three selected 4H-chromenes (compound I, II, and III) against human colon adenocarcinoma cell line (COLO 205) using MTT assay. Cells were treated with increasing concentrations of compound I, II, and III from 20 to 200 µM and incubated for 24 hours. The results were presented as the percentage of viable cells compared to control (untreated cells). At the concentration from 20 to 200 µM, compound I, II and III showed a significant decline in % mean viability on COLO 205 cells from 85.63% to 2.01%, 89.18% to 1.31%, and 68.03 % to 7.42%, respectively. Compound I, II and III significantly exhibited cytotoxic activity against COLO 205 cells with IC50 of  26, 30, and 150 μM, respectively. 

Article Details

How to Cite
1.
Jongrungruangchok S, Pradubyat N, Songsak T, Wongwiwatthananukit S. CYTOTOXIC ACTIVITY OF 4H–CHROMENES ON COLO 205 HUMAN COLON ADENOCARCINOMA CELL LINE. Interprof J Health Sci [Internet]. 2023 Oct. 5 [cited 2024 Dec. 22];14(2):27-32. Available from: https://li05.tci-thaijo.org/index.php/IJHS/article/view/146
Section
Research Articles

References

American Cancer Society, “Cancer Facts and Figures 2015” Reported by the North American Association of Central Cancer Registries (NAACCR). Available at http://www.cancer.org/acs/groups/content/@research/documents/document/acspc-044552.pdf

Berridge, M.V., Herst, P.M., Tan, A.S. 2005.Tetrazolium dyes as tools in cell biology: new insights into their cellular reduction. Biotechnol Annual Rev. 11: 127-152.

Daigle SR, Olhava EJ, Therkelsen CA, Majer CR, Sneeringer CJ, Song J, et al. 2011. Selective killing of mixed lineage leukemia cells by a potent small-molecule DOT1L Inhibitor. Cancer Cell. 20: 53–65.

Gore M, Desai NS. 2014. Characterization of phytochemicals and evaluation of anti-cancer potential of Blumea eriantha DC. Physiol Mol Biol Plants. 4:475-486

Li M, Zhang B, Gu Y. 2012. Facile construction of densely functionalized 4H-chromenes via three-component reactions catalyzed by L-proline. Green Chem.14: 2421-2428.

Pratap R, Ram VJ. 2014. Natural and synthetic chromenes, fused chromenes, and versatility of dihydrobenzo[h]chromenes in organic synthesis. Chem. Rev. 114 (20), 10476–10526.

Thomas N, Zachariah SM. 2013. Pharmacological activities of chromene derivatives: an overview. Asian J Pharm Clin Res. 6(2), 11-15. 36(3): 305-312.

Tominaga H, Ishiyama M, Ohseto F, et al. 1999. A water-soluble tetrazolium salt useful for colorimetric cell viability assay. Anal Commun. 36, 47–50.

Xi J, Zhu X, Feng Y, Huang N, Luo G, Han J, et al. 2013. Development of a novel class of tubulin inhibitors with promising anticancer activities. Mol Cancer Res. 11: 856-864.