Multidrug resistance proteins 1/4 (ABCC1 /4) confer resistance to | 50895
Journal of Clinical Toxicology

Journal of Clinical Toxicology
Open Access

ISSN: 2161-0495

+44 1478 350008

Multidrug resistance proteins 1/4 (ABCC1 /4) confer resistance to arsenic compounds in human myeloid leukemic HL-60 cells

International Toxicology Summit & Expo

November 26-28, 2012 Hilton San Antonio Airport, USA

Naranmandura Hua, Shi Xu and Yan Fang Zhang

AcceptedAbstracts: J Clinic Toxicol

Abstract :

A rsenic trioxide (As 2 O 3 ) is established as one of most effective drugs for treatment of patients with acute promyelocytic leukemia (APL), as well as other types of malignant tumors. However, the non-APL HL-60 cells is resistant to As 2 O 3 , and little is known about the underlying resistance mechanism for As 2 O 3 and its biomethylation products, namely, monomethylarsonous acid (MMA III ) on the treatment of tumors. In the present study, we investigated the molecular mechanisms underlying iAs III and its intermediate metabolite MMA III -induced anticancer effects in the non-APL HL-60 cells. Here, we show that the HL- 60 cells exhibit resistance to inorganic iAs III (IC50=10 μM), but are relatively sensitive to its intermediate MMA III (IC 50 =3.5 μM). Moreover, we found that the multidrug resistance protein 1/4 (MRP1/4), but not MRP2, are expressed in HL-60 cells, which reduced the intracellular arsenic accumulation, and conferred resistance to inorganic iAs III and MMA III . Pretreatment of HL-60 with MK571, an inhibitor of MRP1 and 4, significantly increased iAsIII and MMAIII-induced cytotoxicity and arsenic accumulations, suggesting that the expression of MRP1/4 may lead to HL-60 cells resistance to trivalent arsenic compounds

Biography :

Narenmandula Hua is associate professor in the Department of Pharmacology, Toxicology, and Biochemical Pharmaceutics, College of Pharmaceutical Sciences at Zhejiang University, China. He received a PhD degree in pharmacology and toxicology in 2008 from Chiba University (Japan). Then he completed postdoctoral work at the University of Alberta (Canada) He is currently focused on several topics including arsenic speciation, exposure, metabolism, and health effects; the molecular mechanisms of the carcinogenic effects of thioarsenicals and its metabolism pathway; the role of AS3MT expression in arsenic treatment of patients with acute promyelocytic leukemia (APL), etc