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Effects of roniciclib in preclinical models of anaplastic thyroid cancer

Many human cancers have altered cyclin-dependent kinase activity. Inhibition of cyclin-dependent kinases may arrest cell cycle progression and represents an important strategy in the treatment of malignancies. We evaluated the therapeutic effects of roniciclib, a cyclin-dependent kinase inhibitor, a...

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Autores principales: Lin, Shu-Fu, Lin, Jen-Der, Hsueh, Chuen, Chou, Ting-Chao, Wong, Richard J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5620230/
https://www.ncbi.nlm.nih.gov/pubmed/28978090
http://dx.doi.org/10.18632/oncotarget.19092
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author Lin, Shu-Fu
Lin, Jen-Der
Hsueh, Chuen
Chou, Ting-Chao
Wong, Richard J.
author_facet Lin, Shu-Fu
Lin, Jen-Der
Hsueh, Chuen
Chou, Ting-Chao
Wong, Richard J.
author_sort Lin, Shu-Fu
collection PubMed
description Many human cancers have altered cyclin-dependent kinase activity. Inhibition of cyclin-dependent kinases may arrest cell cycle progression and represents an important strategy in the treatment of malignancies. We evaluated the therapeutic effects of roniciclib, a cyclin-dependent kinase inhibitor, as a treatment for anaplastic thyroid cancer. Roniciclib inhibited anaplastic thyroid cancer cell proliferation in a dose-dependent manner. Roniciclib activated caspase-3 activity and induced apoptosis. Cell cycle progression was arrested in G2/M phase. In vivo, the growth of anaplastic thyroid cancer xenograft tumors was retarded by roniciclib treatment without evidence of toxicity. These data provide a rationale for further clinical evaluation using roniciclib in the treatment of patients with anaplastic thyroid cancer.
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spelling pubmed-56202302017-10-03 Effects of roniciclib in preclinical models of anaplastic thyroid cancer Lin, Shu-Fu Lin, Jen-Der Hsueh, Chuen Chou, Ting-Chao Wong, Richard J. Oncotarget Research Paper Many human cancers have altered cyclin-dependent kinase activity. Inhibition of cyclin-dependent kinases may arrest cell cycle progression and represents an important strategy in the treatment of malignancies. We evaluated the therapeutic effects of roniciclib, a cyclin-dependent kinase inhibitor, as a treatment for anaplastic thyroid cancer. Roniciclib inhibited anaplastic thyroid cancer cell proliferation in a dose-dependent manner. Roniciclib activated caspase-3 activity and induced apoptosis. Cell cycle progression was arrested in G2/M phase. In vivo, the growth of anaplastic thyroid cancer xenograft tumors was retarded by roniciclib treatment without evidence of toxicity. These data provide a rationale for further clinical evaluation using roniciclib in the treatment of patients with anaplastic thyroid cancer. Impact Journals LLC 2017-07-08 /pmc/articles/PMC5620230/ /pubmed/28978090 http://dx.doi.org/10.18632/oncotarget.19092 Text en Copyright: © 2017 Lin et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper
Lin, Shu-Fu
Lin, Jen-Der
Hsueh, Chuen
Chou, Ting-Chao
Wong, Richard J.
Effects of roniciclib in preclinical models of anaplastic thyroid cancer
title Effects of roniciclib in preclinical models of anaplastic thyroid cancer
title_full Effects of roniciclib in preclinical models of anaplastic thyroid cancer
title_fullStr Effects of roniciclib in preclinical models of anaplastic thyroid cancer
title_full_unstemmed Effects of roniciclib in preclinical models of anaplastic thyroid cancer
title_short Effects of roniciclib in preclinical models of anaplastic thyroid cancer
title_sort effects of roniciclib in preclinical models of anaplastic thyroid cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5620230/
https://www.ncbi.nlm.nih.gov/pubmed/28978090
http://dx.doi.org/10.18632/oncotarget.19092
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