Collateral sensitivity as a strategy against cancer multidrug resistance
Tài liệu tham khảo
Akiyama, 1985, Isolation and genetic characterization of human KB cell lines resistant to multiple drugs, Somat. Cell Mol. Genet., 11, 117, 10.1007/BF01534700
al-Shawi, 1993, Characterization of the adenosine triphosphatase activity of Chinese hamster P-glycoprotein, J. Biol. Chem., 268, 4197, 10.1016/S0021-9258(18)53597-3
Aleman, 2003, P-glycoprotein, expressed in multidrug resistant cells, is not responsible for alterations in membrane fluidity or membrane potential, Cancer Res., 63, 3084
Ambudkar, 1999, Biochemical, cellular, and pharmacological aspects of the multidrug transporter, Annu. Rev. Pharmacol. Toxicol., 39, 361, 10.1146/annurev.pharmtox.39.1.361
Barattin, 2010, Iodination of verapamil for a stronger induction of death, through GSH efflux, of cancer cells overexpressing MRP1, Bioorg. Med. Chem., 18, 6265, 10.1016/j.bmc.2010.07.031
Bech-Hansen, 1976, Pleiotropic phenotype of colchicine-resistant CHO cells: cross-resistance and collateral sensitivity, J. Cell. Physiol., 88, 23, 10.1002/jcp.1040880104
Bell, 1998, 2-Deoxy-d-glucose preferentially kills multidrug-resistant human KB carcinoma cell lines by apoptosis, Br. J. Cancer, 78, 1464, 10.1038/bjc.1998.708
Bentley, 1997, The human KB multidrug-resistant cell line KB-C1 is hypersensitive to inhibitors of glycosylation, Cancer Lett., 115, 221, 10.1016/S0304-3835(97)04739-3
Berger, 2005, Multidrug resistance markers P-glycoprotein, multidrug resistance protein 1, and lung resistance protein in non-small cell lung cancer: prognostic implications, J. Cancer Res. Clin. Oncol., 131, 355, 10.1007/s00432-004-0653-9
Brough, 2011, Searching for synthetic lethality in cancer, Curr. Opin. Genet. Dev., 21, 34, 10.1016/j.gde.2010.10.009
Broxterman, 1988, Induction by verapamil of a rapid increase in ATP consumption in multidrug-resistant tumor cells, FASEB J., 2, 2278, 10.1096/fasebj.2.7.3350243
Cairns, 2011, Regulation of cancer cell metabolism, Nat. Rev. Cancer, 11, 85, 10.1038/nrc2981
Calcagno, 2007, ABC drug transporters as molecular targets for the prevention of multidrug resistance and drug–drug interactions, Curr. Drug Deliv., 4, 324, 10.2174/156720107782151241
Callaghan, 1995, Collateral sensitivity of multidrug resistant cells to narcotic analgesics is due to effects on the plasma membrane, Biochim. Biophys. Acta, 1236, 155, 10.1016/0005-2736(95)00042-2
Cano-Gauci, 1987, Action of calcium antagonists on multidrug resistant cells. Specific cytotoxicity independent of increased cancer drug accumulation, Biochem. Pharmacol., 36, 2115, 10.1016/0006-2952(87)90139-0
Cole, 2006, Transport of glutathione and glutathione conjugates by MRP1, Trends Pharmacol. Sci., 27, 438, 10.1016/j.tips.2006.06.008
Farmer, 2005, Targeting the DNA repair defect in BRCA mutant cells as a therapeutic strategy, Nature, 434, 917, 10.1038/nature03445
Fox, 2007, Tariquidar (XR9576): a P-glycoprotein drug efflux pump inhibitor, Expert Rev. Anticancer Ther., 7, 447, 10.1586/14737140.7.4.447
Ganguly, 2010, Targeting mitochondrial cell death pathway to overcome drug resistance with a newly developed iron chelate, PLoS One, 5, e11253, 10.1371/journal.pone.0011253
Genoux-Bastide, 2011, Identification of Xanthones as Selective Killers of Cancer Cells Overexpressing the ABC Transporter MRP1, ChemMedChem, 6, 1478, 10.1002/cmdc.201100102
Goldsborough, 2011, Collateral Sensitivity of Multidrug-Resistant Cells to the Orphan Drug Tiopronin, J. Med. Chem., 54, 4987, 10.1021/jm2001663
Gottesman, 2009, Structure of a multidrug transporter, Nat. Biotechnol., 27, 546, 10.1038/nbt0609-546
Gottesman, 2002, Multidrug resistance in cancer: role of ATP-dependent transporters, Nat. Rev. Cancer, 2, 48, 10.1038/nrc706
Hall, 2011, Synthesis and structure–activity evaluation of isatin-beta-thiosemicarbazones with improved selective activity towards multidrug-resistant cells expressing P-glycoprotein, J. Med. Chem., 54, 5878, 10.1021/jm2006047
Hall, 2009, Is resistance useless? Multidrug resistance and collateral sensitivity, Trends Pharmacol. Sci., 30, 546, 10.1016/j.tips.2009.07.003
Hall, 2009, Synthesis, activity, and pharmacophore development for isatin-beta-thiosemicarbazones with selective activity toward multidrug-resistant cells, J. Med. Chem., 52, 3191, 10.1021/jm800861c
Hanahan, 2011, Hallmarks of cancer: the next generation, Cell, 144, 646, 10.1016/j.cell.2011.02.013
He, 2003, Role of reduced glutathione efflux in apoptosis of immortalized human keratinocytes induced by UVA, J. Biol. Chem., 278, 8058, 10.1074/jbc.M207781200
Helson, 1984, Calcium channel blocker enhancement of anticancer drug cytotoxicity--a review, Cancer Drug Deliv., 1, 353, 10.1089/cdd.1984.1.353
Jansson, 2010, The iron complex of Dp44mT is redox-active and induces hydroxyl radical formation: an EPR study, J. Inorg. Biochem., 104, 1224, 10.1016/j.jinorgbio.2010.07.012
Joly, 1999, Treatment of cystinuria, Pediatr. Nephrol., 13, 945, 10.1007/s004670050736
Kaplan, 1991, The multidrug resistance phenotype: 31P nuclear magnetic resonance characterization and 2-deoxyglucose toxicity, Cancer Res., 51, 1638
Kaplan, 1990, Effects of 2-deoxyglucose on drug-sensitive and drug-resistant human breast cancer cells: toxicity and magnetic resonance spectroscopy studies of metabolism, Cancer Res., 50, 544
Kappus, 1981, Toxic drug effects associated with oxygen metabolism: redox cycling and lipid peroxidation, Experientia, 37, 1233, 10.1007/BF01948335
Karwatsky, 2003, A mechanism for P-glycoprotein-mediated apoptosis as revealed by verapamil hypersensitivity, Biochemistry, 42, 12163, 10.1021/bi034149+
Keenan, 2004, Two-deoxyglucose as an anti-metabolite in human carcinoma cell line RPMI-2650 and drug-resistant variants, Anticancer Res., 24, 433
Kelly, 2010, A pharmacodynamic study of docetaxel in combination with the P-glycoprotein antagonist tariquidar (XR9576) in patients with lung, ovarian, and cervical cancer, Clin. Cancer Res., 17, 569, 10.1158/1078-0432.CCR-10-1725
Koppenol, 2011, Otto Warburg's contributions to current concepts of cancer metabolism, Nat. Rev. Cancer, 11, 325, 10.1038/nrc3038
Kuo, 2011, A unique P-glycoprotein interacting agent displays anticancer activity against hepatocellular carcinoma through inhibition of GRP78 and mTOR pathways, Biochem. Pharmacol., 81, 1136, 10.1016/j.bcp.2011.02.013
Laberge, 2009, P-glycoprotein (ABCB1) modulates collateral sensitivity of a multidrug resistant cell line to verapamil, Arch. Biochem. Biophys., 491, 53, 10.1016/j.abb.2009.09.012
Le, 2004, Iron chelators with high antiproliferative activity up-regulate the expression of a growth inhibitory and metastasis suppressor gene: a link between iron metabolism and proliferation, Blood, 104, 2967, 10.1182/blood-2004-05-1866
Le, 2002, The role of iron in cell cycle progression and the proliferation of neoplastic cells, Biochim. Biophys. Acta, 1603, 31
Leonard, 2003, The role of ABC transporters in clinical practice, Oncologist, 8, 411, 10.1634/theoncologist.8-5-411
Loe, 2000, Verapamil stimulates glutathione transport by the 190-kDa multidrug resistance protein 1 (MRP1), J. Pharmacol. Exp. Ther., 293, 530
Ludwig, 2006, Selective toxicity of NSC73306 in MDR1-positive cells as a new strategy to circumvent multidrug resistance in cancer, Cancer Res., 66, 4808, 10.1158/0008-5472.CAN-05-3322
Lyon, 1988, Glucose metabolism in drug-sensitive and drug-resistant human breast cancer cells monitored by magnetic resonance spectroscopy, Cancer Res., 48, 870
Marks, 2011, The selectivity of austocystin D arises from cell-line-specific drug activation by cytochrome P450 enzymes, J. Nat. Prod., 74, 567, 10.1021/np100429s
Muller, 1994, Verapamil decreases P-glycoprotein expression in multidrug-resistant human leukemic cell lines, Int. J. Cancer, 56, 749, 10.1002/ijc.2910560523
Naito, 1989, Competitive inhibition by verapamil of ATP-dependent high affinity vincristine binding to the plasma membrane of multidrug-resistant K562 cells without calcium ion involvement, Cancer Res., 49, 1452
Nakagawa-Goto, 2008, Antitumor agents 260. New desmosdumotin B analogues with improved in vitro anticancer activity, J. Med. Chem., 51, 3297, 10.1021/jm701208v
Nakagawa-Goto, 2010, Antitumor agents 280. Multidrug resistance-selective desmosdumotin B analogues, J. Med. Chem., 53, 6699, 10.1021/jm100846r
Nobili, 2011, Overcoming tumor multidrug resistance using drugs able to evade P-glycoprotein or to exploit its expression, Med. Res. Rev.
Perrotton, 2007, (R)- and (S)-verapamil differentially modulate the multidrug-resistant protein MRP1, J. Biol. Chem., 282, 31542, 10.1074/jbc.M703964200
Prisant, 2001, Verapamil revisited: a transition in novel drug delivery systems and outcomes, Heart Dis., 3, 55, 10.1097/00132580-200101000-00008
Robey, 2010, The challenge of exploiting ABCG2 in the clinic, Curr. Pharm. Biotechnol., 12, 595, 10.2174/138920111795163913
Robey, 2007, ABCG2: determining its relevance in clinical drug resistance, Cancer Metastasis Rev., 26, 39, 10.1007/s10555-007-9042-6
Szakacs, 2004, Predicting drug sensitivity and resistance: profiling ABC transporter genes in cancer cells, Cancer Cell, 6, 129, 10.1016/j.ccr.2004.06.026
Szakacs, 2006, Targeting multidrug resistance in cancer, Nat. Rev. Drug Discov., 5, 219, 10.1038/nrd1984
Szybalski, 1952, Genetic studies on microbial cross resistance to toxic agents: I. Cross resistance of Escherichia coli to fifteen antibiotics, J. Bacteriol., 64, 489, 10.1128/JB.64.4.489-499.1952
Tran, 2011, Modulation of P-glycoprotein-mediated anticancer drug accumulation, cytotoxicity, and ATPase activity by flavonoid interactions, Nutr. Cancer, 63, 435, 10.1080/01635581.2011.535959
Trompier, 2004, Verapamil and its derivative trigger apoptosis through glutathione extrusion by multidrug resistance protein MRP1, Cancer Res., 64, 4950, 10.1158/0008-5472.CAN-04-0143
Tsuruo, 1983, Circumvention of vincristine and Adriamycin resistance in vitro and in vivo by calcium influx blockers, Cancer Res., 43, 2905
Tsuruo, 1981, Overcoming of vincristine resistance in P388 leukemia in vivo and in vitro through enhanced cytotoxicity of vincristine and vinblastine by verapamil, Cancer Res., 41, 1967
Turk, 2009, Identification of compounds selectively killing multidrug-resistant cancer cells, Cancer Res., 69, 8293, 10.1158/0008-5472.CAN-09-2422
Warr, 1988, Properties of verapamil-hypersensitive multidrug-resistant Chinese hamster ovary cells, Cancer Res., 48, 4477
Warr, 1986, Verapamil hypersensitivity of vincristine resistant Chinese hamster ovary cell lines, Cell Biol. Int. Rep., 10, 389, 10.1016/0309-1651(86)90011-1
Whitnall, 2006, A class of iron chelators with a wide spectrum of potent antitumor activity that overcomes resistance to chemotherapeutics, Proc. Natl. Acad. Sci. U. S. A., 103, 14901, 10.1073/pnas.0604979103
Wu, 2007, Evidence for dual mode of action of a thiosemicarbazone. NSC73306: a potent substrate of the multidrug resistance linked ABCG2 transporter, Mol. Cancer Ther., 6, 3287, 10.1158/1535-7163.MCT-07-2005
Xu, 2005, Inhibition of glycolysis in cancer cells: a novel strategy to overcome drug resistance associated with mitochondrial respiratory defect and hypoxia, Cancer Res., 65, 613, 10.1158/0008-5472.613.65.2
Yuan, 2004, Novel di-2-pyridyl-derived iron chelators with marked and selective antitumor activity: in vitro and in vivo assessment, Blood, 104, 1450, 10.1182/blood-2004-03-0868
Zhou, 2008, Structure, function and regulation of P-glycoprotein and its clinical relevance in drug disposition, Xenobiotica, 38, 802, 10.1080/00498250701867889