Realgar‐induced differentiation is associated with MAPK pathways in HL‐60 cells

Cell Biology International - Tập 32 - Trang 1497-1505 - 2008
Nan Wang1, Li-Wen Wang2, Bao-Di Gou1, Tian-Lan Zhang1,2, Kui Wang1
1Department of Chemical Biology, Peking University School of Pharmaceutical Sciences, 38 Xueyuan Road, Beijing 100083, PR China
2Department of Chemical Biology, Capital Medical University School of Pharmaceutical Sciences, 10 Xitoutiao, You An Men, Beijing 100069, PR China

Tóm tắt

AbstractThe clinical efficacy and safety of realgar (arsenic sulfide, As4S4) in the treatment of acute promyelocytic leukemia in China have given rise to an upsurge in research on the underlying mechanism. We prepared realgar nanoparticles (RNPs) to examine their effect on the differentiation of HL‐60 cells. Treatment with RNPs at 6 μM for 72 h induced cell differentiation that was assessed by morphological change, NBT reductive ability, and elevation of CD11b expression at both mRNA and protein levels. The RNP‐induced differentiation was synergized, enhanced and suppressed by the inhibition of p38 MAPK, JNK and ERK pathways, respectively. Our findings demonstrate that MAPK signaling pathways are closely related to the RNP‐induced differentiation in HL‐60 cells.

Tài liệu tham khảo

10.1074/jbc.270.46.27489 10.1078/0171-9335-00141 Birnie G.D., 1998, The HL60 cell line: a model system for studying human myeloid cell differentiation, Br J Cancer, 41 10.1038/35065000 10.1046/j.1365-2141.2003.04460.x 10.1006/phrs.2001.0885 10.1006/excr.2001.5200 10.1016/S0165-6147(00)01865-4 10.1016/j.leukres.2004.01.011 10.1021/bi980832y 10.2174/1568026054985939 10.1046/j.1365-2141.1998.01079.x 10.1016/S0145-2126(01)00026-1 10.4161/cc.1.6.269 10.1016/j.bbapap.2005.08.017 10.1016/j.ejphar.2005.02.008 10.1093/carcin/bgg179 10.1016/S0162-3109(00)00206-X 10.1016/S0039-9140(03)00274-1 10.1182/blood.V99.9.3136 Mayer R.J., 2006, p38 MAP kinase inhibitors: a future therapy for inflammatory diseases, Drug Disc Today, 3, 49 Miller W.H., 2002, Mechanisms of action of arsenic trioxide, Cancer Res, 62, 3893 10.1038/sj.leu.2402400 10.1016/j.febslet.2006.12.016 10.1016/j.coph.2004.03.009 10.1182/asheducation-2006.1.147 10.1182/blood.V89.9.3354 10.1200/JCO.2001.19.18.3852 10.1111/j.1365-2141.2005.05655.x 10.1152/ajplung.2000.279.5.L895 10.1038/sj.leu.2403916 10.1002/jcb.10595 10.1006/excr.2000.4939 10.1002/1097-4644(20010315)80:4<471::AID-JCB1001>3.0.CO;2-J 10.1007/BF02977662 Wang Z., 2000, Differentiation and apoptosis induction therapy in acute promyelocytic leukaemia, Oncology, 1, 101 10.1634/theoncologist.6-suppl_2-3 10.1016/j.ejps.2006.05.002 10.1385/BTER:103:2:117 10.1007/s11626-999-0063-z 10.1182/blood-2004-04-1433 10.1038/sj.onc.1204762