Two clinical drugs deubiquitinase inhibitor auranofin and aldehyde dehydrogenase inhibitor disulfiram trigger synergistic anti-tumor effects in vitro and in vivo

scientific article published on 28 November 2015

Two clinical drugs deubiquitinase inhibitor auranofin and aldehyde dehydrogenase inhibitor disulfiram trigger synergistic anti-tumor effects in vitro and in vivo is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.18632/ONCOTARGET.6425
P932PMC publication ID4823072
P698PubMed publication ID26625200
P5875ResearchGate publication ID285541977

P50authorXuejun WangQ38361109
P2093author name stringXin Chen
Chong Zhao
Jinbao Liu
Xiaofen Li
Hongbiao Huang
Ningning Liu
Changshan Yang
Dan Zang
Yuning Liao
Xianping Shi
Jinjie Wu
Xiaoying Lan
Huidan Long
Jianyu Cai
Xianliang Hua
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Protein translation and folding are coupled by an endoplasmic-reticulum-resident kinaseQ28296183
Yama/CPP32 beta, a mammalian homolog of CED-3, is a CrmA-inhibitable protease that cleaves the death substrate poly(ADP-ribose) polymeraseQ28302692
A novel small molecule inhibitor of deubiquitylating enzyme USP14 and UCHL5 induces apoptosis in multiple myeloma and overcomes bortezomib resistanceQ28395203
Deubiquitinases (DUBs) and DUB inhibitors: a patent reviewQ28834608
Quantitative analysis of dose-effect relationships: the combined effects of multiple drugs or enzyme inhibitorsQ29547463
A screen for deubiquitinating enzymes involved in the G₂/M checkpoint identifies USP50 as a regulator of HSP90-dependent Wee1 stability.Q34142357
Clinically used antirheumatic agent auranofin is a proteasomal deubiquitinase inhibitor and inhibits tumor growthQ34221890
Auranofin induces lethal oxidative and endoplasmic reticulum stress and exerts potent preclinical activity against chronic lymphocytic leukemiaQ34231446
Physiological levels of ATP negatively regulate proteasome function.Q34376187
L-carnitine is an endogenous HDAC inhibitor selectively inhibiting cancer cell growth in vivo and in vitroQ34472177
HERC2-USP20 axis regulates DNA damage checkpoint through ClaspinQ34579692
Anti-rheumatic agent auranofin induced apoptosis in chronic myeloid leukemia cells resistant to imatinib through both Bcr/Abl-dependent and -independent mechanismsQ34619261
Simultaneous inhibition of deubiquitinating enzymes (DUBs) and autophagy synergistically kills breast cancer cellsQ35551964
Deubiquitinases in cancerQ35955141
Pharmacologic screens reveal metformin that suppresses GRP78-dependent autophagy to enhance the anti-myeloma effect of bortezomib.Q36254571
Translation reinitiation at alternative open reading frames regulates gene expression in an integrated stress responseQ36322641
Gambogic acid enhances proteasome inhibitor-induced anticancer activityQ36869779
Simultaneous inhibition of glutathione- and thioredoxin-dependent metabolism is necessary to potentiate 17AAG-induced cancer cell killing via oxidative stress.Q36879064
Overexpression of USP14 Protease Reduces I-κB Protein Levels and Increases Cytokine Release in Lung Epithelial CellsQ36890519
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Disulfiram eradicates tumor-initiating hepatocellular carcinoma cells in ROS-p38 MAPK pathway-dependent and -independent mannersQ37472766
Gambogic acid induces apoptosis in imatinib-resistant chronic myeloid leukemia cells via inducing proteasome inhibition and caspase-dependent Bcr-Abl downregulationQ37610733
Disulfiram is a direct and potent inhibitor of human O6-methylguanine-DNA methyltransferase (MGMT) in brain tumor cells and mouse brain and markedly increases the alkylating DNA damageQ37616054
Enhancement of auranofin-induced lung cancer cell apoptosis by selenocystine, a natural inhibitor of TrxR1 in vitro and in vivoQ37726102
Deubiquitinases in cancer: new functions and therapeutic options.Q37945451
The biological activity of auranofin: implications for novel treatment of diseasesQ38042341
Deubiquitinase inhibition as a cancer therapeutic strategyQ38274749
Deubiquitinases and the new therapeutic opportunities offered to cancerQ38326071
Controlling the unfolded protein response-mediated life and death decisions in cancer.Q38392861
The de-ubiquitylating enzymes USP26 and USP37 regulate homologous recombination by counteracting RAP80.Q38860961
Copper signaling axis as a target for prostate cancer therapeuticsQ38947366
Systematic characterization of deubiquitylating enzymes for roles in maintaining genome integrityQ38959150
Protective role of humanin on bortezomib-induced bone growth impairment in anticancer treatment.Q39019344
Disulfiram, a drug widely used to control alcoholism, suppresses self-renewal of glioblastoma and overrides resistance to temozolomideQ39263561
Mechanism of UCH-L5 activation and inhibition by DEUBAD domains in RPN13 and INO80G.Q41375336
Potentiation of nitrogen mustard cytotoxicity by disulfiram, diethyldithiocarbamic acid, and diethylamine in miceQ45347622
Disulfiram, a clinically used anti-alcoholism drug and copper-binding agent, induces apoptotic cell death in breast cancer cultures and xenografts via inhibition of the proteasome activityQ48381026
Evaluation of the in vivo antitumor activity and in vitro cytotoxic properties of auranofin, a coordinated gold compound, in murine tumor modelsQ69936658
Two distinct stress signaling pathways converge upon the CHOP promoter during the mammalian unfolded protein responseQ74359929
P433issue3
P407language of work or nameEnglishQ1860
P304page(s)2796-2808
P577publication date2015-11-28
P1433published inOncotargetQ1573155
P1476titleTwo clinical drugs deubiquitinase inhibitor auranofin and aldehyde dehydrogenase inhibitor disulfiram trigger synergistic anti-tumor effects in vitro and in vivo
P478volume7

Reverse relations

cites work (P2860)
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