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Small-molecule inhibition of proteasome and aggresome function induces synergistic antitumor activity in multiple myeloma

https://doi.org/10.1073/pnas.0503221102
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1016/j.molcel.2004.12.021openalex-snapshot
Global Impairment of the Ubiquitin-Proteasome System by Nuclear or Cytoplasmic Protein Aggregates Precedes Inclusion Body Formation
inferredcites →https://doi.org/10.1016/s0092-8674(03)00939-5openalex-snapshot
The Deacetylase HDAC6 Regulates Aggresome Formation and Cell Viability in Response to Misfolded Protein Stress
inferredcites →https://doi.org/10.1016/s0962-8924(00)01852-3openalex-snapshot
Aggresomes, inclusion bodies and protein aggregation
inferredcites →https://doi.org/10.1016/s1074-5521(03)00095-4openalex-snapshot
Multidimensional Chemical Genetic Analysis of Diversity-Oriented Synthesis-Derived Deacetylase Inhibitors Using Cell-Based Assays
inferredcites →https://doi.org/10.1016/s1471-4892(03)00084-5openalex-snapshot
Histone deacetylases
inferredcites →https://doi.org/10.1016/s1535-6108(04)00050-9openalex-snapshot
Inhibition of the insulin-like growth factor receptor-1 tyrosine kinase activity as a therapeutic strategy for multiple myeloma, other hematologic malignancies, and solid tumors
inferredcites →https://doi.org/10.1021/ja0341440openalex-snapshot
Structural Biasing Elements for In-Cell Histone Deacetylase Paralog Selectivity
inferredcites →https://doi.org/10.1034/j.1600-065x.2003.00053.xopenalex-snapshot
Novel therapeutic approaches for multiple myeloma
inferredcites →https://doi.org/10.1034/j.1600-0854.2002.30602.xopenalex-snapshot
Hassles with Taking Out the Garbage: Aggravating Aggresomes
inferredcites →https://doi.org/10.1038/nrc952openalex-snapshot
Molecular mechanisms of novel therapeutic approaches for multiple myeloma
inferredcites →https://doi.org/10.1038/sj.onc.1204623openalex-snapshot
The role of tumor necrosis factor α in the pathophysiology of human multiple myeloma: therapeutic applications
inferredcites →https://doi.org/10.1038/sj.onc.1207170openalex-snapshot
Proteasome inhibitor PS-341 abrogates IL-6 triggered signaling cascades via caspase-dependent downregulation of gp130 in multiple myeloma
inferredcites →https://doi.org/10.1038/sj.onc.1208118openalex-snapshot
p38 MAPK inhibition enhances PS-341 (bortezomib)-induced cytotoxicity against multiple myeloma cells
inferredcites →https://doi.org/10.1056/nejm200406173502526openalex-snapshot
Single versus Double Autologous Stem-Cell Transplantation for Multiple Myeloma
inferredcites →https://doi.org/10.1056/nejmoa030288openalex-snapshot
A Phase 2 Study of Bortezomib in Relapsed, Refractory Myeloma
inferredcites →https://doi.org/10.1056/nejmoa032290openalex-snapshot
Single versus Double Autologous Stem-Cell Transplantation for Multiple Myeloma
inferredcites →https://doi.org/10.1073/pnas.0430973100openalex-snapshot
Domain-selective small-molecule inhibitor of histone deacetylase 6 (HDAC6)-mediated tubulin deacetylation
inferredcites →https://doi.org/10.1073/pnas.202445099openalex-snapshot
Molecular sequelae of proteasome inhibition in human multiple myeloma cells
inferredcites →https://doi.org/10.1074/jbc.m200360200openalex-snapshot
NF-κB as a Therapeutic Target in Multiple Myeloma
inferredcites →https://doi.org/10.1182/blood-2002-06-1768openalex-snapshot
The proteasome inhibitor PS-341 potentiates sensitivity of multiple myeloma cells to conventional chemotherapeutic agents: therapeutic applications
inferredcites →https://doi.org/10.1182/blood-2002-08-2543openalex-snapshot
Molecular mechanisms mediating antimyeloma activity of proteasome inhibitor PS-341
inferredcites →https://doi.org/10.1182/blood-2002-11-3514openalex-snapshot
Molecular sequelae of histone deacetylase inhibition in human malignant B cells
inferredcites →https://doi.org/10.1182/blood-2003-01-0233openalex-snapshot
NVP-LAQ824 is a potent novel histone deacetylase inhibitor with significant activity against multiple myeloma
inferredcites →https://doi.org/10.1182/blood-2004-05-1760openalex-snapshot
VEGF induces Mcl-1 up-regulation and protects multiple myeloma cells against apoptosis
inferredcites →https://doi.org/10.1182/blood-2004-06-2281openalex-snapshot
Combination of the mTOR inhibitor rapamycin and CC-5013 has synergistic activity in multiple myeloma
inferredcites →https://doi.org/10.1182/blood.v82.12.3712.3712openalex-snapshot
Adhesion of human myeloma-derived cell lines to bone marrow stromal cells stimulates interleukin-6 secretion
inferredcites →https://doi.org/10.1200/jco.1992.10.2.334openalex-snapshot
Combination chemotherapy versus melphalan and prednisolone in the treatment of multiple myeloma: an overview of published trials.

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4189784openalex-extracted
The Small Molecular Compound CC1007 Suppresses Multiple Myeloma Via Upregulation of Nur77
inferred← citeshttps://doi.org/10.1002/3527600906.mcb.201100010openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781118592168.ch33openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781119000822.hfcm122openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9783527619375.ch9aopenalex-snapshot
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inferred← citeshttps://doi.org/10.1002/adma.200602098openalex-snapshot
Gold Nanoparticles Inhibit the Proliferation of Multiple Myeloma Cells
inferred← citeshttps://doi.org/10.1002/adtp.202300421openalex-snapshot
Valproate Mediated Proteasome Dysfunctions Induce Apoptosis
inferred← citeshttps://doi.org/10.1002/ajh.24236openalex-snapshot
Myeloma today: Disease definitions and treatment advances
inferred← citeshttps://doi.org/10.1002/ajh.24402openalex-snapshot
Multiple myeloma: 2016 update on diagnosis, risk‐stratification, and management
inferred← citeshttps://doi.org/10.1002/ajh.25117openalex-snapshot
Multiple myeloma: 2018 update on diagnosis, risk‐stratification, and management
inferred← citeshttps://doi.org/10.1002/ajh.25791openalex-snapshot
Multiple myeloma: 2020 update on diagnosis, risk‐stratification and management
inferred← citeshttps://doi.org/10.1002/ange.200703198openalex-snapshot
Fluorous‐Based Small‐Molecule Microarrays for the Discovery of Histone Deacetylase Inhibitors
inferred← citeshttps://doi.org/10.1002/anie.200703198openalex-snapshot
Fluorous‐Based Small‐Molecule Microarrays for the Discovery of Histone Deacetylase Inhibitors
inferred← citeshttps://doi.org/10.1002/bmc.3414openalex-snapshot
Development and validation of a LC‐MS assay for the quantification of ikh12 a novel anti‐tumor candidate in rat plasma and tissues and its application in a pharmacokinetic study
inferred← citeshttps://doi.org/10.1002/cmdc.200800196openalex-snapshot
Pyridylalanine‐Containing Hydroxamic Acids as Selective HDAC6 Inhibitors
inferred← citeshttps://doi.org/10.1002/cmdc.200900082openalex-snapshot
Pyrrole‐Based Hydroxamates and 2‐Aminoanilides: Histone Deacetylase Inhibition and Cellular Activities
inferred← citeshttps://doi.org/10.1002/cmdc.201100007openalex-snapshot
Carbamate Prodrug Concept for Hydroxamate HDAC Inhibitors
inferred← citeshttps://doi.org/10.1002/ddr.20275openalex-snapshot
Newly developed effective anti‐cancer drugs targeting multiple myeloma
inferred← citeshttps://doi.org/10.1002/glia.22624openalex-snapshot
HDAC6 inhibition results in tau acetylation and modulates tau phosphorylation and degradation in oligodendrocytes
inferred← citeshttps://doi.org/10.1002/ijc.28924openalex-snapshot
Combination of proteasome and class I HDAC inhibitors induces apoptosis of NPC cells through an HDAC6-independent ER stress-induced mechanism
inferred← citeshttps://doi.org/10.1002/jcb.22185openalex-snapshot
Histone deacetylase inhibitors: Potential in cancer therapy
inferred← citeshttps://doi.org/10.1002/med.20169openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/med.20178openalex-snapshot
NAD+-dependent histone deacetylases (sirtuins) as novel therapeutic targets
inferred← citeshttps://doi.org/10.1002/med.21972openalex-snapshot
Histone deacetylase‐based dual targeted inhibition in multiple myeloma
inferred← citeshttps://doi.org/10.1002/mnfr.201000547openalex-snapshot
Differential effects of sulforaphane on histone deacetylases, cell cycle arrest and apoptosis in normal prostate cells versus hyperplastic and cancerous prostate cells
inferred← citeshttps://doi.org/10.1002/pbc.24271openalex-snapshot
A phase I trial of vorinostat and bortezomib in children with refractory or recurrent solid tumors: A Children's Oncology Group phase I consortium study (ADVL0916)
inferred← citeshttps://doi.org/10.1002/pmic.201200233openalex-snapshot
Quantitative proteomic analysis to decipher the differential apoptotic response of bortezomib‐treated APL cells before and after retinoic acid differentiation reveals involvement of protein toxicity mechanisms
inferred← citeshttps://doi.org/10.1002/slct.201601117openalex-snapshot
Engineering and In Vitro Evaluation of Acid Labile Cholesterol Tethered MG132 Nanoparticle for Targeting Ubiquitin‐Proteasome System in Cancer
inferred← citeshttps://doi.org/10.1007/978-1-4020-6554-5_12openalex-snapshot
Targeting Proteasomes as Therapy in Multiple Myeloma
inferred← citeshttps://doi.org/10.1007/978-1-4419-0717-2_10openalex-snapshot
Histone Deacetylases (HDAC)
inferred← citeshttps://doi.org/10.1007/978-1-4419-6706-0_4openalex-snapshot
Endoplasmic Reticulum Stress and BCL-2 Family Members
inferred← citeshttps://doi.org/10.1007/978-1-4614-0730-0openalex-snapshot
Cell Signaling & Molecular Targets in Cancer
inferred← citeshttps://doi.org/10.1007/978-1-4614-0730-0_5openalex-snapshot
Signalling Molecules as Selective Targets for Therapeutic Strategies in Multiple Myeloma
inferred← citeshttps://doi.org/10.1007/978-1-4614-3764-2_27openalex-snapshot
Cytokines and Signal Transduction in Multiple Myeloma
inferred← citeshttps://doi.org/10.1007/978-1-4614-4666-8_14openalex-snapshot
Epigenetic Regulation of Myeloma Within Its Bone Marrow Microenvironment
inferred← citeshttps://doi.org/10.1007/978-1-4614-5260-7_9openalex-snapshot
Novel Agents in Multiple Myeloma
inferred← citeshttps://doi.org/10.1007/978-1-4614-6613-0_10-3openalex-snapshot
Histone Deacetylases (HDAC)
inferred← citeshttps://doi.org/10.1007/978-1-59745-474-2_8openalex-snapshot
Histone Deacetylase Inhibitors and Anticancer Activity
inferred← citeshttps://doi.org/10.1007/978-1-59745-564-0_24openalex-snapshot
Histone Deacetylase Inhibitors in Multiple Myeloma
inferred← citeshttps://doi.org/10.1007/978-1-59745-564-0_26openalex-snapshot
Proteasome Inhibitors as Therapy in Multiple Myeloma
inferred← citeshttps://doi.org/10.1007/978-1-59745-564-0_3openalex-snapshot
Basic Biology of Plasma Cell Dyscrasias: Focus on the Role of the Tumor Microenviroment
inferred← citeshttps://doi.org/10.1007/978-1-60327-424-1_10openalex-snapshot
Targeted Therapy in Multiple Myeloma
inferred← citeshttps://doi.org/10.1007/978-1-60761-389-3_29openalex-snapshot
Clinical and Pathologic Issues in Patients with Amyloidosis: Practical Comments Regarding Diagnosis, Therapy, and Solid Organ Transplantation
inferred← citeshttps://doi.org/10.1007/978-3-030-73440-4_7openalex-snapshot
Histone Deacetylase Inhibitors
inferred← citeshttps://doi.org/10.1007/978-3-319-06752-0_1openalex-snapshot
Proteasome Inhibitors and Lessons Learned from Their Mechanisms of Action and Resistance in Human Cancer
inferred← citeshttps://doi.org/10.1007/978-3-319-06752-0_11openalex-snapshot
Proteotoxic Stress and Proteasome Inhibitor Efficacy and Resistance
inferred← citeshttps://doi.org/10.1007/978-3-319-06752-0_2openalex-snapshot
Resistance to Proteasome Inhibitors in Multiple Myeloma
inferred← citeshttps://doi.org/10.1007/978-3-319-06752-0_6openalex-snapshot
Targeting Mantle Cell Lymphoma with a Strategy of Combined Proteasome and Histone Deacetylase Inhibition
inferred← citeshttps://doi.org/10.1007/978-3-319-19294-9_36openalex-snapshot
Clinical and Pathologic Issues in Patients with Amyloidosis: Summary and Practical Comments Regarding Diagnosis, Therapy, and Solid Organ Transplantation
inferred← citeshttps://doi.org/10.1007/978-3-319-40320-5_2openalex-snapshot
Vision Statement for Multiple Myeloma: Future Directions
inferred← citeshttps://doi.org/10.1007/978-3-319-61872-2_5openalex-snapshot
Treatment of Patients in First or Second Relapse
inferred← citeshttps://doi.org/10.1007/978-3-319-75184-9_3openalex-snapshot
Proteasome Inhibitors with a Focus on Bortezomib
inferred← citeshttps://doi.org/10.1007/978-3-540-31209-3_10openalex-snapshot
Clinical Relevance of Targeted Interference with Src-Mediated Signal Transduction Events
inferred← citeshttps://doi.org/10.1007/978-3-540-34594-7_10openalex-snapshot
Histone Deacetylase Inhibitors in APL and Beyond
inferred← citeshttps://doi.org/10.1007/978-3-540-85772-3_8openalex-snapshot
Novel Drugs in Myeloma: Harnessing Tumour Biology to Treat Myeloma
inferred← citeshttps://doi.org/10.1007/978-3-642-01222-8_12openalex-snapshot
Bortezomib
inferred← citeshttps://doi.org/10.1007/978-3-642-38404-2_10openalex-snapshot
Histone Deacetylase (HDAC) Inhibitors in Recent Clinical Trials for Cancer Therapy
inferred← citeshttps://doi.org/10.1007/978-3-642-54490-3_20openalex-snapshot
Bortezomib
inferred← citeshttps://doi.org/10.1007/978-3-7643-8948-2_2openalex-snapshot
Preclinical Activities of Bortezomib in MM, the Bone Marrow Microenvironment and Pharmacogenomics
inferred← citeshttps://doi.org/10.1007/978-3-7643-8948-2_6openalex-snapshot
Bortezomib in Relapsed and Relapsed/Refractory Multiple Myeloma
inferred← citeshttps://doi.org/10.1007/978-3-7643-8989-5_9openalex-snapshot
HDAC Inhibitors and Cancer Therapy
inferred← citeshttps://doi.org/10.1007/978-94-007-0344-5_30openalex-snapshot
Aggravating Endoplasmic Reticulum Stress by Combined Application of Bortezomib and Celecoxib as a Novel Therapeutic Strategy for Glioblastoma
inferred← citeshttps://doi.org/10.1007/978-94-007-2923-0_3openalex-snapshot
Chemoprevention of Prostate Cancer with Cruciferous Vegetables: Role of Epigenetics
inferred← citeshttps://doi.org/10.1007/978-981-15-8179-3_10openalex-snapshot
Combining Histone Deacetylase Inhibitors with Other Anticancer Agents as a Novel Strategy for Circumventing Limited Therapeutic Efficacy and Mitigating Toxicity
inferred← citeshttps://doi.org/10.1007/978-981-96-0301-5_5openalex-snapshot
Relevance of Small Molecule Inhibitors in Advancing Cancer Therapeutics
inferred← citeshttps://doi.org/10.1007/s00018-018-2966-xopenalex-snapshot
Bardet–Biedl Syndrome proteins regulate cilia disassembly during tissue maturation
inferred← citeshttps://doi.org/10.1007/s00253-015-7107-yopenalex-snapshot
Eukaryotic aggresomes: from a model of conformational diseases to an emerging type of immobilized biocatalyzers
inferred← citeshttps://doi.org/10.1007/s00262-023-03624-yopenalex-snapshot
HDAC6 inhibitor ACY-1215 enhances STAT1 acetylation to block PD-L1 for colorectal cancer immunotherapy
inferred← citeshttps://doi.org/10.1007/s00277-006-0239-5openalex-snapshot
Towards a new age in the treatment of multiple myeloma
inferred← citeshttps://doi.org/10.1007/s00280-010-1324-yopenalex-snapshot
Identification of type-specific anticancer histone deacetylase inhibitors: road to success
inferred← citeshttps://doi.org/10.1007/s00280-020-04043-xopenalex-snapshot
Involvement of ER stress and reactive oxygen species generation in anti-cancer effect of CKD-516 for lung cancer
inferred← citeshttps://doi.org/10.1007/s00401-013-1158-xopenalex-snapshot
Inclusion body formation, macroautophagy, and the role of HDAC6 in neurodegeneration
inferred← citeshttps://doi.org/10.1007/s10495-017-1364-4openalex-snapshot
Ricolinostat, a selective HDAC6 inhibitor, shows anti-lymphoma cell activity alone and in combination with bendamustine
inferred← citeshttps://doi.org/10.1007/s10555-006-8500-xopenalex-snapshot
Molecular mechanisms of metastasis
inferred← citeshttps://doi.org/10.1007/s10555-017-9698-5openalex-snapshot
Emerging small molecule approaches to enhance the antimyeloma benefit of proteasome inhibitors
inferred← citeshttps://doi.org/10.1007/s10555-017-9699-4openalex-snapshot
(Immuno)proteasomes as therapeutic target in acute leukemia
inferred← citeshttps://doi.org/10.1007/s10555-017-9707-8openalex-snapshot
The proteasome and proteasome inhibitors in multiple myeloma
inferred← citeshttps://doi.org/10.1007/s10637-010-9589-xopenalex-snapshot
The DAC system and associations with multiple myeloma
inferred← citeshttps://doi.org/10.1007/s10637-010-9596-yopenalex-snapshot
Histone deacetylase inhibitors: potential targets responsible for their anti-cancer effect
inferred← citeshttps://doi.org/10.1007/s11095-010-0318-0openalex-snapshot
Inorganic Nanoparticles in Cancer Therapy
inferred← citeshttps://doi.org/10.1007/s11899-009-0014-5openalex-snapshot
Treatment of relapsed and refractory myeloma
inferred← citeshttps://doi.org/10.1007/s11899-013-0173-2openalex-snapshot
Management of Double-Refractory Multiple Myeloma
inferred← citeshttps://doi.org/10.1007/s11899-016-0312-7openalex-snapshot
Practical Approaches to the Management of Dual Refractory Multiple Myeloma
inferred← citeshttps://doi.org/10.1007/s12032-009-9376-8openalex-snapshot
Future directions in immunomodulatory therapy
inferred← citeshttps://doi.org/10.1007/s12035-017-0558-7openalex-snapshot
UCH-L1 Inhibition Suppresses tau Aggresome Formation during Proteasomal Impairment
inferred← citeshttps://doi.org/10.1007/s12185-011-0917-5openalex-snapshot
Novel therapies in MM: from the aspect of preclinical studies
inferred← citeshttps://doi.org/10.1007/s12185-013-1290-3openalex-snapshot
Histone deacetylase inhibitors in the treatment for multiple myeloma
inferred← citeshttps://doi.org/10.1007/s12185-016-2008-0openalex-snapshot
Histone deacetylase inhibitors in multiple myeloma: from bench to bedside
inferred← citeshttps://doi.org/10.1007/s12185-016-2040-0openalex-snapshot
Mechanisms of action and resistance for multiple myeloma novel drug treatments
inferred← citeshttps://doi.org/10.1007/s12253-011-9432-5openalex-snapshot
Down-Regulated Expression of HSP70 in Correlation with Clinicopathology of Cholangiocarcinoma
inferred← citeshttps://doi.org/10.1007/s12263-012-0283-9openalex-snapshot
Histone deacetylase modulators provided by Mother Nature
inferred← citeshttps://doi.org/10.1007/s13148-010-0012-4openalex-snapshot
Histone deacetylase (HDAC) inhibitors in recent clinical trials for cancer therapy
inferred← citeshttps://doi.org/10.1007/s13402-022-00704-6openalex-snapshot
HDAC6: A unique HDAC family member as a cancer target
inferred← citeshttps://doi.org/10.1007/s40262-017-0565-xopenalex-snapshot
Clinical Pharmacokinetics and Pharmacodynamics of Panobinostat
inferred← citeshttps://doi.org/10.1016/b978-0-12-374145-5.00325-9openalex-snapshot
The Evolution and Maintenance of the Multiple Myeloma Cell Clone within the Liquid Bone Marrow Compartment
inferred← citeshttps://doi.org/10.1016/b978-0-12-394387-3.00004-5openalex-snapshot
HDAC Inhibitor Modulation of Proteotoxicity as a Therapeutic Approach in Cancer
inferred← citeshttps://doi.org/10.1016/b978-0-12-394387-3.00006-9openalex-snapshot
Histone Deacetylase Inhibitors and Rational Combination Therapies
inferred← citeshttps://doi.org/10.1016/b978-0-12-394387-3.00007-0openalex-snapshot
HDAC Inhibitors and Chaperone Function
inferred← citeshttps://doi.org/10.1016/b978-0-12-801944-3.00005-9openalex-snapshot
Targeting Selective Autophagy of Insoluble Protein Aggregates
inferred← citeshttps://doi.org/10.1016/b978-0-12-816435-8.00013-4openalex-snapshot
Proteasome Inhibitors as Sensitizing Agents for Cancer Chemotherapy
inferred← citeshttps://doi.org/10.1016/b978-0-323-47674-4.00101-8openalex-snapshot
Multiple Myeloma and Related Disorders
inferred← citeshttps://doi.org/10.1016/b978-0-323-69538-1.00029-xopenalex-snapshot
Myeloma and Leukemia
inferred← citeshttps://doi.org/10.1016/bs.acr.2015.03.002openalex-snapshot
Emerging Therapeutic Strategies for Overcoming Proteasome Inhibitor Resistance
inferred← citeshttps://doi.org/10.1016/j.addr.2008.03.013openalex-snapshot
Biological properties of “naked” metal nanoparticles☆
inferred← citeshttps://doi.org/10.1016/j.arr.2014.07.002openalex-snapshot
Clearance of misfolded and aggregated proteins by aggrephagy and implications for aggregation diseases
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2010.10.002openalex-snapshot
Protein lysine acetylation in cellular function and its role in cancer manifestation
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2010.06.001openalex-snapshot
Accumulation of polyubiquitylated proteins in response to Ala-Ala-Phe-chloromethylketone is independent of the inhibition of tripeptidyl peptidase II
inferred← citeshttps://doi.org/10.1016/j.bbcan.2022.188676openalex-snapshot
Histone deacetylases: A novel class of therapeutic targets for pancreatic cancer
inferred← citeshttps://doi.org/10.1016/j.bbrc.2006.07.185openalex-snapshot
Histone deacetylase inhibitor trichostatin A and proteasome inhibitor PS-341 synergistically induce apoptosis in pancreatic cancer cells
inferred← citeshttps://doi.org/10.1016/j.bbrc.2008.03.019openalex-snapshot
Inhibition of histone deacetylase1 induces autophagy
inferred← citeshttps://doi.org/10.1016/j.bbrc.2009.08.009openalex-snapshot
The microtubule-targeting agent T0070907 induces proteasomal degradation of tubulin
inferred← citeshttps://doi.org/10.1016/j.bbrc.2016.09.128openalex-snapshot
Mechanism of paclitaxel resistance in a human prostate cancer cell line, PC3-PR, and its sensitization by cabazitaxel
inferred← citeshttps://doi.org/10.1016/j.bcp.2012.06.014openalex-snapshot
Development and therapeutic impact of HDAC6-selective inhibitors
inferred← citeshttps://doi.org/10.1016/j.beha.2007.09.008openalex-snapshot
From the bench to the bedside: emerging new treatments in multiple myeloma
inferred← citeshttps://doi.org/10.1016/j.beha.2012.04.007openalex-snapshot
Proteasome inhibitors in mantle cell lymphoma
inferred← citeshttps://doi.org/10.1016/j.bioactmat.2025.02.040openalex-snapshot
Organelle-oriented nanomedicines in tumor therapy: Targeting, escaping, or collaborating?
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2010.04.007openalex-snapshot
The influence of mediators of intracellular trafficking on transgene expression efficacy of polymer–plasmid DNA complexes
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2019.119604openalex-snapshot
DMSO impairs the transcriptional program for maternal-to-embryonic transition by altering histone acetylation
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105278openalex-snapshot
Development of selective HDAC6 inhibitors with in vitro and in vivo anti-multiple myeloma activity
inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.106217openalex-snapshot
CC1007, a small molecular compound, suppresses multiple myeloma via upregulation of Nur77
inferred← citeshttps://doi.org/10.1016/j.biopha.2020.110454openalex-snapshot
Molecular docking-based virtual drug screening revealing an oxofluorenyl benzamide and a bromonaphthalene sulfonamido hydroxybenzoic acid as HDAC6 inhibitors with cytotoxicity against leukemia cells
inferred← citeshttps://doi.org/10.1016/j.bmc.2007.10.092openalex-snapshot
Phenylalanine-containing hydroxamic acids as selective inhibitors of class IIb histone deacetylases (HDACs)
inferred← citeshttps://doi.org/10.1016/j.bmc.2013.06.009openalex-snapshot
Novel N-hydroxyfurylacrylamide-based histone deacetylase (HDAC) inhibitors with branched CAP group (Part 2)
inferred← citeshttps://doi.org/10.1016/j.bmc.2026.118762openalex-snapshot
Non-covalent dual HDAC6/proteasome inhibitors with anti-multiple myeloma activity
inferred← citeshttps://doi.org/10.1016/j.bmcl.2006.12.117openalex-snapshot
Identification of a potent and stable antiproliferative agent by the prodrug formation of a thiolate histone deacetylase inhibitor
inferred← citeshttps://doi.org/10.1016/j.bmcl.2011.08.027openalex-snapshot
The structural requirements of histone deacetylase inhibitors: Suberoylanilide hydroxamic acid analogs modified at the C3 position display isoform selectivity
inferred← citeshttps://doi.org/10.1016/j.bmcl.2014.10.022openalex-snapshot
Histone deacetylase inhibitors derived from 1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine and related heterocycles selective for the HDAC6 isoform
inferred← citeshttps://doi.org/10.1016/j.canlet.2008.03.037openalex-snapshot
Histone deacetylase inhibitors: Mechanisms of cell death and promise in combination cancer therapy
inferred← citeshttps://doi.org/10.1016/j.canlet.2008.07.005openalex-snapshot
Endoplasmic reticulum stress and autophagy as targets for cancer therapy
inferred← citeshttps://doi.org/10.1016/j.canlet.2008.08.016openalex-snapshot
HDAC family: What are the cancer relevant targets?
inferred← citeshttps://doi.org/10.1016/j.canlet.2009.01.040openalex-snapshot
Histone deacetylase inhibitors that target tubulin
inferred← citeshttps://doi.org/10.1016/j.canlet.2009.02.013openalex-snapshot
Isoform-specific histone deacetylase inhibitors: The next step?
inferred← citeshttps://doi.org/10.1016/j.canlet.2009.02.019openalex-snapshot
Development of the pan-DAC inhibitor panobinostat (LBH589): Successes and challenges
inferred← citeshttps://doi.org/10.1016/j.canlet.2012.06.016openalex-snapshot
Molecular crosstalk between the proteasome, aggresomes and autophagy: Translational potential and clinical implications
inferred← citeshttps://doi.org/10.1016/j.canlet.2017.01.033openalex-snapshot
HDAC6 deacetylates p53 at lysines 381/382 and differentially coordinates p53-induced apoptosis
inferred← citeshttps://doi.org/10.1016/j.canlet.2019.02.003openalex-snapshot
Proteasome inhibitor b-AP15 induces enhanced proteotoxicity by inhibiting cytoprotective aggresome formation
inferred← citeshttps://doi.org/10.1016/j.ccr.2013.11.001openalex-snapshot
A bis-Benzylidine Piperidone Targeting Proteasome Ubiquitin Receptor RPN13/ADRM1 as a Therapy for Cancer
inferred← citeshttps://doi.org/10.1016/j.cell.2007.04.035openalex-snapshot
HEF1-Dependent Aurora A Activation Induces Disassembly of the Primary Cilium
inferred← citeshttps://doi.org/10.1016/j.chembiol.2022.12.007openalex-snapshot
Inhibitors of the ATPase p97/VCP: From basic research to clinical applications
inferred← citeshttps://doi.org/10.1016/j.clml.2013.03.016openalex-snapshot
Histone Deacetylase Inhibitors in Multiple Myeloma: Rationale and Evidence for Their Use in Combination Therapy
inferred← citeshttps://doi.org/10.1016/j.clml.2016.02.042openalex-snapshot
VANTAGE 095: An International, Multicenter, Open-Label Study of Vorinostat (MK-0683) in Combination With Bortezomib in Patients With Relapsed and Refractory Multiple Myeloma
inferred← citeshttps://doi.org/10.1016/j.clml.2017.05.007openalex-snapshot
Final Results of a Phase 1 Study of Vorinostat, Pegylated Liposomal Doxorubicin, and Bortezomib in Relapsed or Refractory Multiple Myeloma
inferred← citeshttps://doi.org/10.1016/j.clml.2018.03.002openalex-snapshot
An Expanded Treatment Protocol of Panobinostat Plus Bortezomib and Dexamethasone in Patients With Previously Treated Myeloma
inferred← citeshttps://doi.org/10.1016/j.clml.2020.07.013openalex-snapshot
Phase 1 Trial Evaluating Vorinostat Plus Bortezomib, Lenalidomide, and Dexamethasone in Patients With Newly Diagnosed Multiple Myeloma
inferred← citeshttps://doi.org/10.1016/j.clml.2020.11.019openalex-snapshot
Bortezomib, Vorinostat, and Dexamethasone Combination Therapy in Relapsed Myeloma: Results of the Phase 2 MUK four Trial
inferred← citeshttps://doi.org/10.1016/j.clml.2021.06.020openalex-snapshot
Panobinostat From Bench to Bedside: Rethinking the Treatment Paradigm for Multiple Myeloma
inferred← citeshttps://doi.org/10.1016/j.cmonc.2012.02.009openalex-snapshot
Bench-to-bedside translation of targeted therapies in multiple myeloma
inferred← citeshttps://doi.org/10.1016/j.coph.2006.03.010openalex-snapshot
Histone deacetylase inhibitors: gathering pace
inferred← citeshttps://doi.org/10.1016/j.ctrv.2011.04.001openalex-snapshot
Targeted therapies for advanced non-small-cell lung cancer: Current status and future implications
inferred← citeshttps://doi.org/10.1016/j.ctrv.2018.09.001openalex-snapshot
Drug resistance in multiple myeloma
inferred← citeshttps://doi.org/10.1016/j.drup.2008.08.002openalex-snapshot
Mechanisms of proteasome inhibitor action and resistance in cancer
inferred← citeshttps://doi.org/10.1016/j.drup.2010.04.003openalex-snapshot
Macroautophagy modulates cellular response to proteasome inhibitors in cancer therapy
inferred← citeshttps://doi.org/10.1016/j.drup.2014.12.001openalex-snapshot
Molecular basis of resistance to proteasome inhibitors in hematological malignancies
inferred← citeshttps://doi.org/10.1016/j.ejmech.2021.113874openalex-snapshot
Inhibition of Histone Deacetylase 6 (HDAC6) as a therapeutic strategy for Alzheimer's disease: A review (2010–2020)
inferred← citeshttps://doi.org/10.1016/j.ejmech.2024.116435openalex-snapshot
Research strategies of small molecules as chemotherapeutics to overcome multiple myeloma resistance
inferred← citeshttps://doi.org/10.1016/j.ejmech.2024.117208openalex-snapshot
Synthesis and functional screening of novel inhibitors targeting the HDAC6 zinc finger ubiquitin-binding domain
inferred← citeshttps://doi.org/10.1016/j.ejphar.2025.178303openalex-snapshot
Doxorubicin-mediated retardation of aggresome formation enhances Carfilzomib-induced cell death synergistically by augmenting ER stress and proapoptotic signaling
inferred← citeshttps://doi.org/10.1016/j.ejphar.2026.178721openalex-snapshot
Bridging protein quality control and epigenetic dysregulation: The HDAC6 paradox in neurological disorders and therapeutic targeting
inferred← citeshttps://doi.org/10.1016/j.exphem.2007.01.024openalex-snapshot
Targeted therapy of multiple myeloma based upon tumor-microenvironmental interactions
inferred← citeshttps://doi.org/10.1016/j.exphem.2015.04.010openalex-snapshot
Novel therapeutic strategies for multiple myeloma
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2012.09.023openalex-snapshot
Histone deacetylase 6 (HDAC6) plays a crucial role in p38MAPK-dependent induction of heme oxygenase-1 (HO-1) in response to proteasome inhibition
inferred← citeshttps://doi.org/10.1016/j.hoc.2007.08.013openalex-snapshot
Preclinical Studies of Novel Targeted Therapies
inferred← citeshttps://doi.org/10.1016/j.hoc.2010.08.013openalex-snapshot
Protein Quality Control During Erythropoiesis and Hemoglobin Synthesis
inferred← citeshttps://doi.org/10.1016/j.hoc.2012.01.006openalex-snapshot
Role of Histone Deacetylase Inhibitors in the Treatment of Lymphomas and Multiple Myeloma
inferred← citeshttps://doi.org/10.1016/j.hoc.2014.07.001openalex-snapshot
Novel Targeted Agents in the Treatment of Multiple Myeloma
inferred← citeshttps://doi.org/10.1016/j.hoc.2016.11.002openalex-snapshot
Novel Agents in the Treatment of Relapsed or Refractory Peripheral T-Cell Lymphoma
inferred← citeshttps://doi.org/10.1016/j.hoc.2023.12.016openalex-snapshot
Proteasome Inhibitors in Multiple Myeloma
inferred← citeshttps://doi.org/10.1016/j.jns.2011.02.017openalex-snapshot
HDAC6 α-tubulin deacetylase: A potential therapeutic target in neurodegenerative diseases
inferred← citeshttps://doi.org/10.1016/j.jprot.2019.01.009openalex-snapshot
A large scale proteome analysis of the gefitinib primary resistance overcome by KDAC inhibition in KRAS mutated adenocarcinoma cells overexpressing amphiregulin
inferred← citeshttps://doi.org/10.1016/j.jss.2013.03.052openalex-snapshot
Synergistic inhibition of thyroid cancer by suppressing MAPK/PI3K/AKT pathways
inferred← citeshttps://doi.org/10.1016/j.kint.2016.01.026openalex-snapshot
Inhibition of histone deacetylase 6 activity reduces cyst growth in polycystic kidney disease
inferred← citeshttps://doi.org/10.1016/j.leukres.2010.04.001openalex-snapshot
Combined proteasome and histone deacetylase inhibition: A promising synergy for patients with relapsed/refractory multiple myeloma
inferred← citeshttps://doi.org/10.1016/j.leukres.2012.02.026openalex-snapshot
HDAC6 as a target for antileukemic drugs in acute myeloid leukemia
inferred← citeshttps://doi.org/10.1016/j.leukres.2012.02.029openalex-snapshot
Bortezomib and panobinostat combination is effective against PTCL
inferred← citeshttps://doi.org/10.1016/j.leukres.2013.03.006openalex-snapshot
Preclinical data and early clinical experience supporting the use of histone deacetylase inhibitors in multiple myeloma
inferred← citeshttps://doi.org/10.1016/j.leukres.2020.106398openalex-snapshot
A452, HDAC6-selective inhibitor synergistically enhances the anticancer activity of immunomodulatory drugs in IMiDs-resistant multiple myeloma
inferred← citeshttps://doi.org/10.1016/j.lfs.2025.123749openalex-snapshot
PSME2 promotes malignant progression through autophagy modulation via IL-6/STAT3 signaling pathway in esophageal squamous cell carcinoma
inferred← citeshttps://doi.org/10.1016/j.mayocp.2015.11.007openalex-snapshot
Multiple Myeloma: Diagnosis and Treatment
inferred← citeshttps://doi.org/10.1016/j.mayocp.2017.01.003openalex-snapshot
Therapy for Relapsed Multiple Myeloma
inferred← citeshttps://doi.org/10.1016/j.niox.2007.01.001openalex-snapshot
Hydroxyurea increases eNOS protein levels through inhibition of proteasome activity
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2014.04.004openalex-snapshot
Histone deacetylase inhibitor (HDACI) mechanisms of action: Emerging insights
inferred← citeshttps://doi.org/10.1016/j.phrs.2015.08.002openalex-snapshot
Transcriptional dysregulation in Huntington’s disease: The role of histone deacetylases
inferred← citeshttps://doi.org/10.1016/j.phrs.2017.11.004openalex-snapshot
Anti-cancer effects of naturally derived compounds targeting histone deacetylase 6-related pathways
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2017.08.005openalex-snapshot
Progressing neurobiological strategies against proteostasis failure: Challenges in neurodegeneration
inferred← citeshttps://doi.org/10.1016/j.treopn.2026.08.003openalex-snapshot
Nondegradative ubiquitination organizes therapy-relevant stress assemblies
inferred← citeshttps://doi.org/10.1016/j.virol.2008.02.034openalex-snapshot
Susceptibility to virus–cell fusion at the plasma membrane is reduced through expression of HIV gp41 cytoplasmic domains
inferred← citeshttps://doi.org/10.1016/j.virusres.2012.12.006openalex-snapshot
African swine fever virus-cell interactions: From virus entry to cell survival
inferred← citeshttps://doi.org/10.1016/j.ymgme.2008.03.012openalex-snapshot
The aggresome pathway as a target for therapy in hematologic malignancies
inferred← citeshttps://doi.org/10.1016/s0140-6736(09)60221-xopenalex-snapshot
Multiple myeloma
inferred← citeshttps://doi.org/10.1016/s1016-8478(23)14003-9openalex-snapshot
Proteotoxic Stress and Cell Lifespan Control
inferred← citeshttps://doi.org/10.1016/s1470-2045(08)70304-8openalex-snapshot
New drugs in multiple myeloma: mechanisms of action and phase I/II clinical findings
inferred← citeshttps://doi.org/10.1016/s1470-2045(11)70327-8openalex-snapshot
Histone deacetylase inhibitors and Hodgkin's lymphoma
inferred← citeshttps://doi.org/10.1016/s1470-2045(13)70398-xopenalex-snapshot
Vorinostat or placebo in combination with bortezomib in patients with multiple myeloma (VANTAGE 088): a multicentre, randomised, double-blind study
inferred← citeshttps://doi.org/10.1016/s1470-2045(14)70443-7openalex-snapshot
Panobinostat for the treatment of multiple myeloma
inferred← citeshttps://doi.org/10.1016/s1470-2045(16)30375-8openalex-snapshot
Ricolinostat plus lenalidomide, and dexamethasone in relapsed or refractory multiple myeloma: a multicentre phase 1b trial
inferred← citeshttps://doi.org/10.1016/s2352-3026(15)00097-6openalex-snapshot
Panobinostat in combination with bortezomib in patients with relapsed or refractory peripheral T-cell lymphoma: an open-label, multicentre phase 2 trial
inferred← citeshttps://doi.org/10.1016/s2352-3026(15)00116-7openalex-snapshot
Combination therapy for relapsed peripheral T-cell lymphoma: is two better than one?
inferred← citeshttps://doi.org/10.1016/s2352-3026(16)30165-xopenalex-snapshot
Bortezomib, thalidomide, dexamethasone, and panobinostat for patients with relapsed multiple myeloma (MUK-six): a multicentre, open-label, phase 1/2 trial
inferred← citeshttps://doi.org/10.1017/cbo9780511551901.005openalex-snapshot
TREATMENT OF RELAPSED AND RELAPSED/REFRACTORY MULTIPLE MYELOMA
inferred← citeshttps://doi.org/10.1017/cbo9780511862465.009openalex-snapshot
Principles of pathway directed therapy
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