Antitumour effects of selected plant polyphenols, gallic acid and ellagic acid, on sensitive and multidrug‐resistant leukaemia HL60 cells

• Published in: Phytotherapy research Vol. 33; no. 4; pp. 1208 - 1221
• Main Authors: Maruszewska, Agnieszka, Tarasiuk, Jolanta
• Format: Journal Article
• Language: English
• Published: England Wiley Subscription Services, Inc 01-04-2019
• Subjects: Acids; Anticancer properties; Apoptosis; Caspase; Cell death; Cytotoxicity; DNA fragmentation; DNA topoisomerase (ATP-hydrolysing); Ellagic acid; Gallic acid; Glycoproteins; leukaemia HL60 cells; Leukemia; Lysosomes; multidrug resistance; Multidrug resistant organisms; Phenolic acids; Phenols; Phenotypes; Polyphenols; programmed cell death; Reactive oxygen species; Time dependence; multidrug resistance; leukaemia HL60 cells; ellagic acid; programmed cell death; gallic acid; reactive oxygen species
• ISSN: 0951-418X; 1099-1573
• DOI: 10.1002/ptr.6317

The aim of this study was to examine the antitumour effects of plant phenolic acids, gallic acid (GA) and ellagic acid (EA), on human promyelocytic leukaemia sensitive HL60 cell line and its resistant sublines exhibiting two MDR phenotypes: HL60/VINC (overexpressing P‐glycoprotein) and HL60/MX2 (characterized by the presence of mutated α isoform of topoisomerase II). Both studied compounds exerted comparable cytotoxic activities towards sensitive HL60 cells and their MDR counterparts. It was also found that GA and EA modulated the cellular level of reactive oxygen species in a dose‐dependent and time‐dependent manner. Furthermore, it was demonstrated that GA (IC90) and EA (IC50 and IC90) significantly increased the percentage of sub‐G1 subpopulation of all studied leukaemia cells causing oligonucleosomal DNA fragmentation. Both compounds used at IC90 triggered mainly the apoptotic death of these cells. However, GA had no effect on the activity of caspase‐3 as well as caspase‐8 in sensitive HL60 cells and their MDR counterparts. In contrast, EA provoked a significant activation of these caspases in all studied leukaemia cells. It was also found that lysosomes were not involved in triggering programmed death of sensitive HL60 and MDR cells by GA and EA.