Combination of Sulindac and Dichloroacetate Kills Cancer Cells via Oxidative Damage

被引:51
作者
Ayyanathan, Kasirajan [1 ,2 ]
Kesaraju, Shailaja [1 ]
Dawson-Scully, Ken [1 ,2 ]
Weissbach, Herbert [1 ]
机构
[1] Florida Atlantic Univ, Charles E Schmidt Coll Sci, Ctr Mol Biol & Biotechnol, Jupiter, FL USA
[2] Florida Atlantic Univ, Dept Biol Sci, Charles E Schmidt Coll Sci, Boca Raton, FL 33431 USA
基金
美国国家卫生研究院;
关键词
CONGENITAL LACTIC-ACIDOSIS; CYCLOOXYGENASE-2; INHIBITORS; HYDROGEN-PEROXIDE; ARSENIC TRIOXIDE; IN-VITRO; APOPTOSIS; STRESS; INDUCTION; GROWTH; DEHYDROGENASE;
D O I
10.1371/journal.pone.0039949
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Sulindac is an FDA-approved non-steroidal anti-inflammatory drug with documented anticancer activities. Our recent studies showed that sulindac selectively enhanced the killing of cancer cells exposed to oxidizing agents via production of reactive oxygen species (ROS) resulting in mitochondrial dysfunction. This effect of sulindac and oxidative stress on cancer cells could be related to the defect in respiration in cancer cells, first described by Warburg 50 years ago, known as the Warburg effect. We postulated that sulindac might enhance the selective killing of cancer cells when combined with any compound that alters mitochondrial respiration. To test this hypothesis we have used dichloroacetate (DCA), which is known to shift pyruvate metabolism away from lactic acid formation to respiration. One might expect that DCA, since it stimulates aerobic metabolism, could stress mitochondrial respiration in cancer cells, which would result in enhanced killing in the presence of sulindac. In this study, we have shown that the combination of sulindac and DCA enhances the selective killing of A549 and SCC25 cancer cells under the conditions used. As predicted, the mechanism of killing involves ROS production, mitochondrial dysfunction, JNK signaling and death by apoptosis. Our results suggest that the sulindac-DCA drug combination may provide an effective cancer therapy.
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页数:12
相关论文
共 42 条
[1]
Mitochondrial O2-• and H2O2 mediate glucose deprivation-induced cytotoxicity and oxidative stress in human cancer cells [J].
Ahmad, IM ;
Aykin-Burns, N ;
Sim, JE ;
Walsh, SA ;
Higashikubo, R ;
Buettner, GR ;
Venkataraman, S ;
Mackey, MA ;
Flanagan, SW ;
Oberley, LW ;
Spitz, DR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (06) :4254-4263
[2]
Cyclooxygenase-independent induction of apoptosis by sulindac sulfone is mediated by polyamines in colon cancer [J].
Babbar, N ;
Ignatenko, NA ;
Casero, RA ;
Gerner, EW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (48) :47762-47775
[3]
A mitochondria-K+ channel axis is suppressed in cancer and its normalization promotes apoptosis and inhibits cancer growth [J].
Bonnet, Sebastien ;
Archer, Stephen L. ;
Allalunis-Turner, Joan ;
Haromy, Alois ;
Beaulieu, Christian ;
Thompson, Richard ;
Lee, Christopher T. ;
Lopaschuk, Gary D. ;
Puttagunta, Lakshmi ;
Bonnet, Sandra ;
Harry, Gwyneth ;
Hashimoto, Kyoko ;
Porter, Christopher J. ;
Andrade, Miguel A. ;
Thebaud, Bernard ;
Michelakis, Evangelos D. .
CANCER CELL, 2007, 11 (01) :37-51
[4]
Boolbol SK, 1996, CANCER RES, V56, P2556
[5]
Dichloroacetate (DCA) sensitizes both wild-type and over expressing Bcl-2 prostate cancer cells in vitro to radiation [J].
Cao, Wengang ;
Yacoub, Saif ;
Shiverick, Kathleen T. ;
Namiki, Kazunori ;
Sakai, Yoshihisa ;
Porvasnik, Stacy ;
Urbanek, Cydney ;
Rosser, Charles J. .
PROSTATE, 2008, 68 (11) :1223-1231
[6]
QUANTITATIVE-ANALYSIS OF DOSE-EFFECT RELATIONSHIPS - THE COMBINED EFFECTS OF MULTIPLE-DRUGS OR ENZYME-INHIBITORS [J].
CHOU, TC ;
TALALAY, P .
ADVANCES IN ENZYME REGULATION, 1984, 22 :27-55
[7]
USE OF AN AQUEOUS SOLUBLE TETRAZOLIUM FORMAZAN ASSAY FOR CELL-GROWTH ASSAYS IN CULTURE [J].
CORY, AH ;
OWEN, TC ;
BARLTROP, JA ;
CORY, JG .
CANCER COMMUNICATIONS, 1991, 3 (07) :207-212
[8]
Brick by brick: metabolism and tumor cell growth [J].
DeBerardinis, Ralph J. ;
Sayed, Nabil ;
Ditsworth, Dara ;
Thompson, Craig B. .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2008, 18 (01) :54-61
[9]
Understanding the Warburg Effect: The Metabolic Requirements of Cell Proliferation [J].
Heiden, Matthew G. Vander ;
Cantley, Lewis C. ;
Thompson, Craig B. .
SCIENCE, 2009, 324 (5930) :1029-1033
[10]
Dichloroacetate metabolically targeted therapy defeats cytotoxicity of standard anticancer drugs [J].
Heshe, Dirk ;
Hoogestraat, Stephanie ;
Brauckmann, Christine ;
Karst, Uwe ;
Boos, Joachim ;
Lanvers-Kaminsky, Claudia .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2011, 67 (03) :647-655