The investigational aurora kinase A inhibitor MLN8237 induces defects in cell viability and cell-cycle progression in malignant bladder cancer cells in vitro and in vivo

10.1158/1078-0432.CCR-12-2383

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Main Authors: Zhou, N, Singh, K, Mir, M.C, Parker, Y, Lindner, D, Dreicer, R, Ecsedy, J.A, Zhang, Z, Teh, B.T, Almasan, A, Hansel, D.E
Other Authors: DUKE-NUS MEDICAL SCHOOL
Format: Article
Published: 2020
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Online Access:https://scholarbank.nus.edu.sg/handle/10635/180801
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spelling sg-nus-scholar.10635-1808012023-08-29T09:55:50Z The investigational aurora kinase A inhibitor MLN8237 induces defects in cell viability and cell-cycle progression in malignant bladder cancer cells in vitro and in vivo Zhou, N Singh, K Mir, M.C Parker, Y Lindner, D Dreicer, R Ecsedy, J.A Zhang, Z Teh, B.T Almasan, A Hansel, D.E DUKE-NUS MEDICAL SCHOOL alisertib gemcitabine paclitaxel aneuploidy animal experiment animal model antineoplastic activity apoptosis article bladder papilloma cancer inhibition cell cycle arrest controlled study drug cytotoxicity drug potentiation gene expression regulation gene overexpression gene sequence human human cell in vitro study in vivo study microarray analysis mouse nonhuman priority journal reverse transcription polymerase chain reaction upregulation Aneuploidy Animals Apoptosis Azepines Cell Cycle Cell Cycle Checkpoints Cell Line, Tumor Cell Survival Cluster Analysis Deoxycytidine Drug Synergism Gene Expression Gene Expression Profiling Humans M Phase Cell Cycle Checkpoints Mice Neoplasm Invasiveness Paclitaxel Phenotype Protein-Serine-Threonine Kinases Pyrimidines Tumor Burden Urinary Bladder Neoplasms Xenograft Model Antitumor Assays 10.1158/1078-0432.CCR-12-2383 Clinical Cancer Research 19 7 1717-1728 2020-10-27T04:47:47Z 2020-10-27T04:47:47Z 2013 Article Zhou, N, Singh, K, Mir, M.C, Parker, Y, Lindner, D, Dreicer, R, Ecsedy, J.A, Zhang, Z, Teh, B.T, Almasan, A, Hansel, D.E (2013). The investigational aurora kinase A inhibitor MLN8237 induces defects in cell viability and cell-cycle progression in malignant bladder cancer cells in vitro and in vivo. Clinical Cancer Research 19 (7) : 1717-1728. ScholarBank@NUS Repository. https://doi.org/10.1158/1078-0432.CCR-12-2383 1078-0432 https://scholarbank.nus.edu.sg/handle/10635/180801 Attribution 4.0 International http://creativecommons.org/licenses/by/4.0/ Unpaywall 20201031
institution National University of Singapore
building NUS Library
continent Asia
country Singapore
Singapore
content_provider NUS Library
collection ScholarBank@NUS
topic alisertib
gemcitabine
paclitaxel
aneuploidy
animal experiment
animal model
antineoplastic activity
apoptosis
article
bladder papilloma
cancer inhibition
cell cycle arrest
controlled study
drug cytotoxicity
drug potentiation
gene expression regulation
gene overexpression
gene sequence
human
human cell
in vitro study
in vivo study
microarray analysis
mouse
nonhuman
priority journal
reverse transcription polymerase chain reaction
upregulation
Aneuploidy
Animals
Apoptosis
Azepines
Cell Cycle
Cell Cycle Checkpoints
Cell Line, Tumor
Cell Survival
Cluster Analysis
Deoxycytidine
Drug Synergism
Gene Expression
Gene Expression Profiling
Humans
M Phase Cell Cycle Checkpoints
Mice
Neoplasm Invasiveness
Paclitaxel
Phenotype
Protein-Serine-Threonine Kinases
Pyrimidines
Tumor Burden
Urinary Bladder Neoplasms
Xenograft Model Antitumor Assays
spellingShingle alisertib
gemcitabine
paclitaxel
aneuploidy
animal experiment
animal model
antineoplastic activity
apoptosis
article
bladder papilloma
cancer inhibition
cell cycle arrest
controlled study
drug cytotoxicity
drug potentiation
gene expression regulation
gene overexpression
gene sequence
human
human cell
in vitro study
in vivo study
microarray analysis
mouse
nonhuman
priority journal
reverse transcription polymerase chain reaction
upregulation
Aneuploidy
Animals
Apoptosis
Azepines
Cell Cycle
Cell Cycle Checkpoints
Cell Line, Tumor
Cell Survival
Cluster Analysis
Deoxycytidine
Drug Synergism
Gene Expression
Gene Expression Profiling
Humans
M Phase Cell Cycle Checkpoints
Mice
Neoplasm Invasiveness
Paclitaxel
Phenotype
Protein-Serine-Threonine Kinases
Pyrimidines
Tumor Burden
Urinary Bladder Neoplasms
Xenograft Model Antitumor Assays
Zhou, N
Singh, K
Mir, M.C
Parker, Y
Lindner, D
Dreicer, R
Ecsedy, J.A
Zhang, Z
Teh, B.T
Almasan, A
Hansel, D.E
The investigational aurora kinase A inhibitor MLN8237 induces defects in cell viability and cell-cycle progression in malignant bladder cancer cells in vitro and in vivo
description 10.1158/1078-0432.CCR-12-2383
author2 DUKE-NUS MEDICAL SCHOOL
author_facet DUKE-NUS MEDICAL SCHOOL
Zhou, N
Singh, K
Mir, M.C
Parker, Y
Lindner, D
Dreicer, R
Ecsedy, J.A
Zhang, Z
Teh, B.T
Almasan, A
Hansel, D.E
format Article
author Zhou, N
Singh, K
Mir, M.C
Parker, Y
Lindner, D
Dreicer, R
Ecsedy, J.A
Zhang, Z
Teh, B.T
Almasan, A
Hansel, D.E
author_sort Zhou, N
title The investigational aurora kinase A inhibitor MLN8237 induces defects in cell viability and cell-cycle progression in malignant bladder cancer cells in vitro and in vivo
title_short The investigational aurora kinase A inhibitor MLN8237 induces defects in cell viability and cell-cycle progression in malignant bladder cancer cells in vitro and in vivo
title_full The investigational aurora kinase A inhibitor MLN8237 induces defects in cell viability and cell-cycle progression in malignant bladder cancer cells in vitro and in vivo
title_fullStr The investigational aurora kinase A inhibitor MLN8237 induces defects in cell viability and cell-cycle progression in malignant bladder cancer cells in vitro and in vivo
title_full_unstemmed The investigational aurora kinase A inhibitor MLN8237 induces defects in cell viability and cell-cycle progression in malignant bladder cancer cells in vitro and in vivo
title_sort investigational aurora kinase a inhibitor mln8237 induces defects in cell viability and cell-cycle progression in malignant bladder cancer cells in vitro and in vivo
publishDate 2020
url https://scholarbank.nus.edu.sg/handle/10635/180801
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