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Apoptosis of leukemia K562 and Molt-4 cells induced by emamectin benzoate involving mitochondrial membrane potential loss and intracellular Ca 2+ modulation.

Authors :
Yun X
Rao W
Xiao C
Huang Q
Source :
Environmental toxicology and pharmacology [Environ Toxicol Pharmacol] 2017 Jun; Vol. 52, pp. 280-287. Date of Electronic Publication: 2017 Apr 19.
Publication Year :
2017

Abstract

Leukemia threatens millions of people's health and lives, and the pesticide-induced leukemia has been increasingly concerned because of the etiologic exposure. In this paper, cytotoxic effect of emamectin benzoate (EMB), an excellent natural-product insecticide, was evaluated through monitoring cell viability, cell apoptosis, mitochondrial membrane potential and intracellular Ca <superscript>2+</superscript> concentration ([Ca <superscript>2+</superscript> ] <subscript>i</subscript> ) in leukemia K562 and Molt-4 cells. Following the exposure to EMB, cell viability was decreased and positive apoptosis of K562 and Molt-4 cells was increased in a concentration- and time- dependent fashion. In the treatment of 10μM EMB, apoptotic cells accounted for 93.0% to K562 cells and 98.9% to Molt-4 cells based on the control, meanwhile, 63.47% of K562 cells and 81.15% of Molt-4 cells exhibited late apoptotic and necrotic features with damaged cytoplasmic membrane. 48h exposure to 10μM EMB increased significantly the great number of cells with mitochondrial membrane potential (MMP) loss, and the elevation of [Ca <superscript>2+</superscript> ] <subscript>i</subscript> level was peaked and persisted within 70s in K562 cells whilst 50s in Molt-4 cells. Moreover, a stronger cytotoxicity of EMB was further observed than that of imatinib. The results authenticate the efficacious effect of EMB as a potential anti-leukemia agent and an inconsistency with regard to insecticide-induced leukemia.<br /> (Copyright © 2017 Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1872-7077
Volume :
52
Database :
MEDLINE
Journal :
Environmental toxicology and pharmacology
Publication Type :
Academic Journal
Accession number :
28525847
Full Text :
https://doi.org/10.1016/j.etap.2017.04.013