Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/75553
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dc.contributor.authorFah Chueahongthongen_US
dc.contributor.authorSingkome Timaen_US
dc.contributor.authorSawitree Chiampanichayakulen_US
dc.contributor.authorCory Berklanden_US
dc.contributor.authorSongyot Anuchapreedaen_US
dc.date.accessioned2022-10-16T07:00:42Z-
dc.date.available2022-10-16T07:00:42Z-
dc.date.issued2021-10-01en_US
dc.identifier.issn14203049en_US
dc.identifier.other2-s2.0-85115703147en_US
dc.identifier.other10.3390/molecules26195785en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85115703147&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/75553-
dc.description.abstractThis study aims to enhance efficacy and reduce toxicity of the combination treatment of a drug and curcumin (Cur) on leukemic stem cell and leukemic cell lines, including KG-1a and KG-1 (FLT3+ LSCs), EoL-1 (FLT3+ LCs), and U937 (FLT3− LCs). The cytotoxicity of co-treatments of doxorubicin (Dox) or idarubicin (Ida) at concentrations of the IC10–IC80 values and each concentration of Cur at the IC20, IC30, IC40, and IC50 values (conditions 1, 2, 3, and 4) was determined by MTT assays. Dox–Cur increased cytotoxicity in leukemic cells. Dox–Cur co-treatment showed additive and synergistic effects in several conditions. The effect of this co-treatment on FLT3 expression in KG-1a, KG-1, and EoL-1 cells was examined by Western blotting. Dox–Cur decreased FLT3 protein levels and total cell numbers in all the cell lines in a dose-dependent manner. In summary, this study exhibits a novel report of Dox–Cur co-treatment in both enhancing cytotoxicity of Dox and inhibiting cell proliferation via FLT3 protein expression in leukemia stem cells and leukemic cells. This is the option of leukemia treatment with reducing side effects of chemotherapeutic drugs to leukemia patients.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleCo-treatments of edible curcumin from turmeric rhizomes and chemotherapeutic drugs on cytotoxicity and FLT3 protein expression in leukemic stem cellsen_US
dc.typeJournalen_US
article.title.sourcetitleMoleculesen_US
article.volume26en_US
article.stream.affiliationsUniversity of Kansas School of Pharmacyen_US
article.stream.affiliationsChiang Mai Universityen_US
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