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Flavopiridol causes cell cycle inhibition and demonstrates anti-cancer activity in anaplastic thyroid cancer models

Anaplastic thyroid cancer (ATC) is a rare, but nearly uniformly fatal disease that is typically resistant to chemotherapy and radiation. Alternative strategies to target this cancer at a molecular level are necessary in order to improve dismal outcomes for ATC patients. We examined the effects of fl...

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Autores principales: Pinto, Nicole, Prokopec, Stephenie D., Ghasemi, Farhad, Meens, Jalna, Ruicci, Kara M., Khan, Imran M., Mundi, Neil, Patel, Krupal, Han, Myung W., Yoo, John, Fung, Kevin, MacNeil, Danielle, Mymryk, Joe S., Datti, Alessandro, Barrett, John W., Boutros, Paul C., Ailles, Laurie, Nichols, Anthony C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7514001/
https://www.ncbi.nlm.nih.gov/pubmed/32970704
http://dx.doi.org/10.1371/journal.pone.0239315
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author Pinto, Nicole
Prokopec, Stephenie D.
Ghasemi, Farhad
Meens, Jalna
Ruicci, Kara M.
Khan, Imran M.
Mundi, Neil
Patel, Krupal
Han, Myung W.
Yoo, John
Fung, Kevin
MacNeil, Danielle
Mymryk, Joe S.
Datti, Alessandro
Barrett, John W.
Boutros, Paul C.
Ailles, Laurie
Nichols, Anthony C.
author_facet Pinto, Nicole
Prokopec, Stephenie D.
Ghasemi, Farhad
Meens, Jalna
Ruicci, Kara M.
Khan, Imran M.
Mundi, Neil
Patel, Krupal
Han, Myung W.
Yoo, John
Fung, Kevin
MacNeil, Danielle
Mymryk, Joe S.
Datti, Alessandro
Barrett, John W.
Boutros, Paul C.
Ailles, Laurie
Nichols, Anthony C.
author_sort Pinto, Nicole
collection PubMed
description Anaplastic thyroid cancer (ATC) is a rare, but nearly uniformly fatal disease that is typically resistant to chemotherapy and radiation. Alternative strategies to target this cancer at a molecular level are necessary in order to improve dismal outcomes for ATC patients. We examined the effects of flavopiridol, a CDK inhibitor, in a panel of ATC cell lines. When cell lines were treated over a ten-point concentration range, CAL62, KMH2 and BHT-101 cell lines had a sub micromolar half-maximal inhibitory concentration, while no effect was seen in the non-cancerous cell line IMR-90. Flavopiridol treatment resulted in decreased levels of the cell cycle proteins CDK9 and MCL1, and induced cell cycle arrest. Flavopiridol also decreased the in vitro ability of ATC cells to form colonies and impeded migration using a transwell migration assay. In vivo, flavopiridol decreased tumor weight and tumor volume over time in a patient-derived xenograft model of ATC. Given the observed in vitro and in vivo activity, flavopiridol warrants further investigation for treatment of ATC.
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spelling pubmed-75140012020-10-01 Flavopiridol causes cell cycle inhibition and demonstrates anti-cancer activity in anaplastic thyroid cancer models Pinto, Nicole Prokopec, Stephenie D. Ghasemi, Farhad Meens, Jalna Ruicci, Kara M. Khan, Imran M. Mundi, Neil Patel, Krupal Han, Myung W. Yoo, John Fung, Kevin MacNeil, Danielle Mymryk, Joe S. Datti, Alessandro Barrett, John W. Boutros, Paul C. Ailles, Laurie Nichols, Anthony C. PLoS One Research Article Anaplastic thyroid cancer (ATC) is a rare, but nearly uniformly fatal disease that is typically resistant to chemotherapy and radiation. Alternative strategies to target this cancer at a molecular level are necessary in order to improve dismal outcomes for ATC patients. We examined the effects of flavopiridol, a CDK inhibitor, in a panel of ATC cell lines. When cell lines were treated over a ten-point concentration range, CAL62, KMH2 and BHT-101 cell lines had a sub micromolar half-maximal inhibitory concentration, while no effect was seen in the non-cancerous cell line IMR-90. Flavopiridol treatment resulted in decreased levels of the cell cycle proteins CDK9 and MCL1, and induced cell cycle arrest. Flavopiridol also decreased the in vitro ability of ATC cells to form colonies and impeded migration using a transwell migration assay. In vivo, flavopiridol decreased tumor weight and tumor volume over time in a patient-derived xenograft model of ATC. Given the observed in vitro and in vivo activity, flavopiridol warrants further investigation for treatment of ATC. Public Library of Science 2020-09-24 /pmc/articles/PMC7514001/ /pubmed/32970704 http://dx.doi.org/10.1371/journal.pone.0239315 Text en © 2020 Pinto et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Pinto, Nicole
Prokopec, Stephenie D.
Ghasemi, Farhad
Meens, Jalna
Ruicci, Kara M.
Khan, Imran M.
Mundi, Neil
Patel, Krupal
Han, Myung W.
Yoo, John
Fung, Kevin
MacNeil, Danielle
Mymryk, Joe S.
Datti, Alessandro
Barrett, John W.
Boutros, Paul C.
Ailles, Laurie
Nichols, Anthony C.
Flavopiridol causes cell cycle inhibition and demonstrates anti-cancer activity in anaplastic thyroid cancer models
title Flavopiridol causes cell cycle inhibition and demonstrates anti-cancer activity in anaplastic thyroid cancer models
title_full Flavopiridol causes cell cycle inhibition and demonstrates anti-cancer activity in anaplastic thyroid cancer models
title_fullStr Flavopiridol causes cell cycle inhibition and demonstrates anti-cancer activity in anaplastic thyroid cancer models
title_full_unstemmed Flavopiridol causes cell cycle inhibition and demonstrates anti-cancer activity in anaplastic thyroid cancer models
title_short Flavopiridol causes cell cycle inhibition and demonstrates anti-cancer activity in anaplastic thyroid cancer models
title_sort flavopiridol causes cell cycle inhibition and demonstrates anti-cancer activity in anaplastic thyroid cancer models
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7514001/
https://www.ncbi.nlm.nih.gov/pubmed/32970704
http://dx.doi.org/10.1371/journal.pone.0239315
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