Belinostat exerts antitumor cytotoxicity through the ubiquitin-proteasome pathway in lung squamous cell carcinoma

10.1002/1878-0261.12064

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Main Authors: Kong, L.R, Tan, T.Z, Ong, W.R, Bi, C, Huynh, H, Lee, S.C, Chng, W.J, Eichhorn, P.J.A, Goh, B.C
Other Authors: CANCER SCIENCE INSTITUTE OF SINGAPORE
Format: Article
Published: Wiley Blackwell 2020
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Online Access:https://scholarbank.nus.edu.sg/handle/10635/173836
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spelling sg-nus-scholar.10635-1738362024-04-18T03:09:11Z Belinostat exerts antitumor cytotoxicity through the ubiquitin-proteasome pathway in lung squamous cell carcinoma Kong, L.R Tan, T.Z Ong, W.R Bi, C Huynh, H Lee, S.C Chng, W.J Eichhorn, P.J.A Goh, B.C CANCER SCIENCE INSTITUTE OF SINGAPORE MEDICINE PHARMACOLOGY B Raf kinase belinostat beta actin caspase 3 cisplatin F box protein f box protein 3 f box protein W10 histone deacetylase 1 histone deacetylase 2 histone deacetylase 3 histone deacetylase 4 histone deacetylase 5 mitogen activated protein kinase mitogen activated protein kinase 1 mitogen activated protein kinase 3 mitogen activated protein kinase kinase 1 mitogen activated protein kinase kinase 2 mitogen activated protein kinase p38 nicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase proteasome protein c jun protein kinase B sirtuin 1 SOS protein STAT2 protein STAT3 protein STAT5 protein STAT6 protein ubiquitin unclassified drug antineoplastic agent belinostat hydroxamic acid proteasome sulfonamide tumor protein ubiquitin animal cell animal experiment animal model animal tissue apoptosis Article cancer inhibition cancer resistance cancer size cell proliferation cell viability chemosensitization combination drug therapy concentration response controlled study cytotoxicity down regulation drug potentiation enzyme activation enzyme degradation enzyme phosphorylation female gene expression histone acetylation human human cell IC50 in vivo study lung cancer cell line mouse nonhuman nucleotide sequence phosphoproteomics priority journal RNA interference signal transduction squamous cell carcinoma cell line squamous cell lung carcinoma transcription regulation treatment duration upregulation drug effects lung tumor MAPK signaling metabolism pathology squamous cell carcinoma tumor cell line Antineoplastic Agents Carcinoma, Squamous Cell Cell Line, Tumor Humans Hydroxamic Acids Lung Neoplasms MAP Kinase Signaling System Neoplasm Proteins Proteasome Endopeptidase Complex Sulfonamides Ubiquitin 10.1002/1878-0261.12064 Molecular Oncology 11 8 965-980 2020-09-01T07:51:50Z 2020-09-01T07:51:50Z 2017-07 Article Kong, L.R, Tan, T.Z, Ong, W.R, Bi, C, Huynh, H, Lee, S.C, Chng, W.J, Eichhorn, P.J.A, Goh, B.C (2017-07). Belinostat exerts antitumor cytotoxicity through the ubiquitin-proteasome pathway in lung squamous cell carcinoma. Molecular Oncology 11 (8) : 965-980. ScholarBank@NUS Repository. https://doi.org/10.1002/1878-0261.12064 15747891 https://scholarbank.nus.edu.sg/handle/10635/173836 Wiley Blackwell Unpaywall 20200831
institution National University of Singapore
building NUS Library
continent Asia
country Singapore
Singapore
content_provider NUS Library
collection ScholarBank@NUS
topic B Raf kinase
belinostat
beta actin
caspase 3
cisplatin
F box protein
f box protein 3
f box protein W10
histone deacetylase 1
histone deacetylase 2
histone deacetylase 3
histone deacetylase 4
histone deacetylase 5
mitogen activated protein kinase
mitogen activated protein kinase 1
mitogen activated protein kinase 3
mitogen activated protein kinase kinase 1
mitogen activated protein kinase kinase 2
mitogen activated protein kinase p38
nicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase
proteasome
protein c jun
protein kinase B
sirtuin 1
SOS protein
STAT2 protein
STAT3 protein
STAT5 protein
STAT6 protein
ubiquitin
unclassified drug
antineoplastic agent
belinostat
hydroxamic acid
proteasome
sulfonamide
tumor protein
ubiquitin
animal cell
animal experiment
animal model
animal tissue
apoptosis
Article
cancer inhibition
cancer resistance
cancer size
cell proliferation
cell viability
chemosensitization
combination drug therapy
concentration response
controlled study
cytotoxicity
down regulation
drug potentiation
enzyme activation
enzyme degradation
enzyme phosphorylation
female
gene expression
histone acetylation
human
human cell
IC50
in vivo study
lung cancer cell line
mouse
nonhuman
nucleotide sequence
phosphoproteomics
priority journal
RNA interference
signal transduction
squamous cell carcinoma cell line
squamous cell lung carcinoma
transcription regulation
treatment duration
upregulation
drug effects
lung tumor
MAPK signaling
metabolism
pathology
squamous cell carcinoma
tumor cell line
Antineoplastic Agents
Carcinoma, Squamous Cell
Cell Line, Tumor
Humans
Hydroxamic Acids
Lung Neoplasms
MAP Kinase Signaling System
Neoplasm Proteins
Proteasome Endopeptidase Complex
Sulfonamides
Ubiquitin
spellingShingle B Raf kinase
belinostat
beta actin
caspase 3
cisplatin
F box protein
f box protein 3
f box protein W10
histone deacetylase 1
histone deacetylase 2
histone deacetylase 3
histone deacetylase 4
histone deacetylase 5
mitogen activated protein kinase
mitogen activated protein kinase 1
mitogen activated protein kinase 3
mitogen activated protein kinase kinase 1
mitogen activated protein kinase kinase 2
mitogen activated protein kinase p38
nicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase
proteasome
protein c jun
protein kinase B
sirtuin 1
SOS protein
STAT2 protein
STAT3 protein
STAT5 protein
STAT6 protein
ubiquitin
unclassified drug
antineoplastic agent
belinostat
hydroxamic acid
proteasome
sulfonamide
tumor protein
ubiquitin
animal cell
animal experiment
animal model
animal tissue
apoptosis
Article
cancer inhibition
cancer resistance
cancer size
cell proliferation
cell viability
chemosensitization
combination drug therapy
concentration response
controlled study
cytotoxicity
down regulation
drug potentiation
enzyme activation
enzyme degradation
enzyme phosphorylation
female
gene expression
histone acetylation
human
human cell
IC50
in vivo study
lung cancer cell line
mouse
nonhuman
nucleotide sequence
phosphoproteomics
priority journal
RNA interference
signal transduction
squamous cell carcinoma cell line
squamous cell lung carcinoma
transcription regulation
treatment duration
upregulation
drug effects
lung tumor
MAPK signaling
metabolism
pathology
squamous cell carcinoma
tumor cell line
Antineoplastic Agents
Carcinoma, Squamous Cell
Cell Line, Tumor
Humans
Hydroxamic Acids
Lung Neoplasms
MAP Kinase Signaling System
Neoplasm Proteins
Proteasome Endopeptidase Complex
Sulfonamides
Ubiquitin
Kong, L.R
Tan, T.Z
Ong, W.R
Bi, C
Huynh, H
Lee, S.C
Chng, W.J
Eichhorn, P.J.A
Goh, B.C
Belinostat exerts antitumor cytotoxicity through the ubiquitin-proteasome pathway in lung squamous cell carcinoma
description 10.1002/1878-0261.12064
author2 CANCER SCIENCE INSTITUTE OF SINGAPORE
author_facet CANCER SCIENCE INSTITUTE OF SINGAPORE
Kong, L.R
Tan, T.Z
Ong, W.R
Bi, C
Huynh, H
Lee, S.C
Chng, W.J
Eichhorn, P.J.A
Goh, B.C
format Article
author Kong, L.R
Tan, T.Z
Ong, W.R
Bi, C
Huynh, H
Lee, S.C
Chng, W.J
Eichhorn, P.J.A
Goh, B.C
author_sort Kong, L.R
title Belinostat exerts antitumor cytotoxicity through the ubiquitin-proteasome pathway in lung squamous cell carcinoma
title_short Belinostat exerts antitumor cytotoxicity through the ubiquitin-proteasome pathway in lung squamous cell carcinoma
title_full Belinostat exerts antitumor cytotoxicity through the ubiquitin-proteasome pathway in lung squamous cell carcinoma
title_fullStr Belinostat exerts antitumor cytotoxicity through the ubiquitin-proteasome pathway in lung squamous cell carcinoma
title_full_unstemmed Belinostat exerts antitumor cytotoxicity through the ubiquitin-proteasome pathway in lung squamous cell carcinoma
title_sort belinostat exerts antitumor cytotoxicity through the ubiquitin-proteasome pathway in lung squamous cell carcinoma
publisher Wiley Blackwell
publishDate 2020
url https://scholarbank.nus.edu.sg/handle/10635/173836
_version_ 1800914194333171712