Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/71336
Title: Cytotoxic and Antiproliferative Effects of Diarylheptanoids Isolated from Curcuma comosa Rhizomes on Leukaemic Cells
Authors: Natsima Viriyaadhammaa
Aroonchai Saiai
Waranya Neimkhum
Wariya Nirachonkul
Wantida Chaiyana
Sawitree Chiampanichayakul
Singkome Tima
Toyonobu Usuki
Suwit Duangmano
Songyot Anuchapreeda
Keywords: Biochemistry, Genetics and Molecular Biology
Chemistry
Pharmacology, Toxicology and Pharmaceutics
Issue Date: 23-Nov-2020
Abstract: Curcuma comosa belongs to the Zingiberaceae family. In this study, two natural compounds were isolated from C. comosa, and their structures were determined using nuclear magnetic resonance. The isolated compounds were identified as 7-(3,4-dihydroxyphenyl)-5-hydroxy-1-phenyl-(1E)-1-heptene (1) and trans-1,7-diphenyl-5-hydroxy-1-heptene (2). Compound 1 showed the strongest cytotoxicity effect against HL-60 cells, while its antioxidant and anti-inflammatory properties were stronger than those of compound 2. Compound 1 proved to be a potent antioxidant, compared to ascorbic acid. Neither compounds had any effect on red blood cell haemolysis. Furthermore, compound 1 significantly decreased Wilms' tumour 1 protein expression and cell proliferation in KG-1a cells. Compound 1 decreased the WT1 protein levels in a time- and dose- dependent manner. Compound 1 suppressed cell cycle at the S phase. In conclusion, compound 1 has a promising chemotherapeutic potential against leukaemia.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85096816566&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/71336
ISSN: 14203049
Appears in Collections:CMUL: Journal Articles

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