Parthenolide induces significant apoptosis and production of reactive oxygen species in high-risk pre-B leukemia cells

被引:73
作者
Zunino, Susan J.
Ducore, Jonathan M.
Storms, David H.
机构
[1] Univ Calif Davis, Western Human Nutr Res Ctr, Agr Res Serv, USDA, Davis, CA 95616 USA
[2] Univ Calif Davis, Sch Med, UC Davis Canc Ctr, Dept Hematol Oncol, Sacramento, CA 95817 USA
关键词
D O I
10.1016/j.canlet.2007.03.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We investigated whether parthenolide, the principal bioactive component of the herb feverfew (Tanacetum parthenium) induced apoptosis in pre-B acute lymphoblastic leukemia (ALL) lines, including cells carrying the t(4;11)(q21;q23) chromosomal translocation. Parthenolide induced rapid apoptotic cell death distinguished by loss of nuclear DNA, externalization of cell membrane phosphatidylserine, and depolarization of mitochondrial membranes at concentrations ranging from 5 to 100 μM. Using reactive oxygen species (ROS)-specific dyes, an increase in nitric oxide and superoxide anion was detected in the cells by 4 h after exposure to parthenolide. Parthenolide-induced elevation of hypochlorite anion was observed only in the two t(4;11) lines. These data suggest parthenolide may have potential as a potent and novel therapeutic agent against pre-B ALLs. © 2007 Elsevier Ireland Ltd. All rights reserved.
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收藏
页码:119 / 127
页数:9
相关论文
共 28 条
[1]   Pharmacological activity of feverfew (Tanacetum parthenium (L) Schultz-Bip): Assessment by inhibition of human polymorphonuclear leukocyte chemiluminescence in-vitro [J].
Brown, AMG ;
Edwards, CM ;
Davey, MR ;
Power, JB ;
Lowe, KC .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1997, 49 (05) :558-561
[2]   NANOMOLAR CONCENTRATIONS OF NITRIC-OXIDE REVERSIBLY INHIBIT SYNAPTOSOMAL RESPIRATION BY COMPETING WITH OXYGEN AT CYTOCHROME-OXIDASE [J].
BROWN, GC ;
COOPER, CE .
FEBS LETTERS, 1994, 356 (2-3) :295-298
[3]   REVERSIBLE INHIBITION OF CYTOCHROME-C-OXIDASE, THE TERMINAL ENZYME OF THE MITOCHONDRIAL RESPIRATORY-CHAIN, BY NITRIC-OXIDE - IMPLICATIONS FOR NEURODEGENERATIVE DISEASES [J].
CLEETER, MWJ ;
COOPER, JM ;
DARLEYUSMAR, VM ;
MONCADA, S ;
SCHAPIRA, AHV .
FEBS LETTERS, 1994, 345 (01) :50-54
[4]   MITOCHONDRIAL MODIFICATIONS DURING RAT THYMOCYTE APOPTOSIS - A STUDY AT THE SINGLE-CELL LEVEL [J].
COSSARIZZA, A ;
KALASHNIKOVA, G ;
GRASSILLI, E ;
CHIAPPELLI, F ;
SALVIOLI, S ;
CAPRI, M ;
BARBIERI, D ;
TROIANO, L ;
MONTI, D ;
FRANCESCHI, C .
EXPERIMENTAL CELL RESEARCH, 1994, 214 (01) :323-330
[5]  
Dörrie J, 2001, CANCER RES, V61, P4731
[6]  
DORRIE J, 2001, CANC LETT, P33
[7]   A FAST AND EASY METHOD TO DETERMINE THE PRODUCTION OF REACTIVE OXYGEN INTERMEDIATES BY HUMAN AND MURINE PHAGOCYTES USING DIHYDRORHODAMINE-123 [J].
EMMENDORFFER, A ;
HECHT, M ;
LOHMANNMATTHES, ML ;
ROESLER, J .
JOURNAL OF IMMUNOLOGICAL METHODS, 1990, 131 (02) :269-275
[8]   Distinct modes of cell death induced by different reactive oxygen species - Amino acyl chloramines mediate hypochlorous acid-induced apoptosis [J].
Englert, RP ;
Shacter, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (23) :20518-20526
[9]   Clinical significance of cytogenetic abnormalities in adult acute lymphoblastic leukemia [J].
Faderl, S ;
Kantarjian, HM ;
Talpaz, M ;
Estrov, Z .
BLOOD, 1998, 91 (11) :3995-4019
[10]   KINETICS AND MECHANISMS OF HYPOCHLOROUS ACID REACTIONS [J].
FOLKES, LK ;
CANDEIAS, LP ;
WARDMAN, P .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1995, 323 (01) :120-126