scholarly article | Q13442814 |
P50 | author | Xuejun Wang | Q38361109 |
P2093 | author name string | Xin 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 | |||
P2860 | cites work | Regulation of cell cycle progression and gene expression by H2A deubiquitination | Q24296401 |
Inhibition of 19S proteasome-associated deubiquitinases by metal-containing compounds | Q28082497 | ||
Protein translation and folding are coupled by an endoplasmic-reticulum-resident kinase | Q28296183 | ||
Yama/CPP32 beta, a mammalian homolog of CED-3, is a CrmA-inhibitable protease that cleaves the death substrate poly(ADP-ribose) polymerase | Q28302692 | ||
A novel small molecule inhibitor of deubiquitylating enzyme USP14 and UCHL5 induces apoptosis in multiple myeloma and overcomes bortezomib resistance | Q28395203 | ||
Deubiquitinases (DUBs) and DUB inhibitors: a patent review | Q28834608 | ||
Quantitative analysis of dose-effect relationships: the combined effects of multiple drugs or enzyme inhibitors | Q29547463 | ||
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 growth | Q34221890 | ||
Auranofin induces lethal oxidative and endoplasmic reticulum stress and exerts potent preclinical activity against chronic lymphocytic leukemia | Q34231446 | ||
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 vitro | Q34472177 | ||
HERC2-USP20 axis regulates DNA damage checkpoint through Claspin | Q34579692 | ||
Anti-rheumatic agent auranofin induced apoptosis in chronic myeloid leukemia cells resistant to imatinib through both Bcr/Abl-dependent and -independent mechanisms | Q34619261 | ||
Simultaneous inhibition of deubiquitinating enzymes (DUBs) and autophagy synergistically kills breast cancer cells | Q35551964 | ||
Deubiquitinases in cancer | Q35955141 | ||
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 response | Q36322641 | ||
Gambogic acid enhances proteasome inhibitor-induced anticancer activity | Q36869779 | ||
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 Cells | Q36890519 | ||
Reverse the curse--the role of deubiquitination in cell cycle control | Q37112275 | ||
Disulfiram eradicates tumor-initiating hepatocellular carcinoma cells in ROS-p38 MAPK pathway-dependent and -independent manners | Q37472766 | ||
Gambogic acid induces apoptosis in imatinib-resistant chronic myeloid leukemia cells via inducing proteasome inhibition and caspase-dependent Bcr-Abl downregulation | Q37610733 | ||
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 damage | Q37616054 | ||
Enhancement of auranofin-induced lung cancer cell apoptosis by selenocystine, a natural inhibitor of TrxR1 in vitro and in vivo | Q37726102 | ||
Deubiquitinases in cancer: new functions and therapeutic options. | Q37945451 | ||
The biological activity of auranofin: implications for novel treatment of diseases | Q38042341 | ||
Deubiquitinase inhibition as a cancer therapeutic strategy | Q38274749 | ||
Deubiquitinases and the new therapeutic opportunities offered to cancer | Q38326071 | ||
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 therapeutics | Q38947366 | ||
Systematic characterization of deubiquitylating enzymes for roles in maintaining genome integrity | Q38959150 | ||
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 temozolomide | Q39263561 | ||
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 mice | Q45347622 | ||
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 activity | Q48381026 | ||
Evaluation of the in vivo antitumor activity and in vitro cytotoxic properties of auranofin, a coordinated gold compound, in murine tumor models | Q69936658 | ||
Two distinct stress signaling pathways converge upon the CHOP promoter during the mammalian unfolded protein response | Q74359929 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 2796-2808 | |
P577 | publication date | 2015-11-28 | |
P1433 | published in | Oncotarget | Q1573155 |
P1476 | title | Two clinical drugs deubiquitinase inhibitor auranofin and aldehyde dehydrogenase inhibitor disulfiram trigger synergistic anti-tumor effects in vitro and in vivo | |
P478 | volume | 7 |
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Q37440054 | Nickel pyrithione induces apoptosis in chronic myeloid leukemia cells resistant to imatinib via both Bcr/Abl-dependent and Bcr/Abl-independent mechanisms. |
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