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Comparison of Transcriptomic Profiles of MiaPaCa-2 Pancreatic Cancer Cells Treated with Different Statins

Statins have been widely used for the treatment of hypercholesterolemia due to their ability to inhibit HMG-CoA reductase, the rate-limiting enzyme of de novo cholesterol synthesis, via the so-called mevalonate pathway. However, their inhibitory action also causes depletion of downstream intermediat...

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Detalles Bibliográficos
Autores principales: Rimpelová, Silvie, Kolář, Michal, Strnad, Hynek, Ruml, Tomáš, Vítek, Libor, Gbelcová, Helena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8226792/
https://www.ncbi.nlm.nih.gov/pubmed/34207840
http://dx.doi.org/10.3390/molecules26123528
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author Rimpelová, Silvie
Kolář, Michal
Strnad, Hynek
Ruml, Tomáš
Vítek, Libor
Gbelcová, Helena
author_facet Rimpelová, Silvie
Kolář, Michal
Strnad, Hynek
Ruml, Tomáš
Vítek, Libor
Gbelcová, Helena
author_sort Rimpelová, Silvie
collection PubMed
description Statins have been widely used for the treatment of hypercholesterolemia due to their ability to inhibit HMG-CoA reductase, the rate-limiting enzyme of de novo cholesterol synthesis, via the so-called mevalonate pathway. However, their inhibitory action also causes depletion of downstream intermediates of the pathway, resulting in the pleiotropic effects of statins, including the beneficial impact in the treatment of cancer. In our study, we compared the effect of all eight existing statins on the expression of genes, the products of which are implicated in cancer inhibition and suggested the molecular mechanisms of their action in epigenetic and posttranslational regulation, and in cell-cycle arrest, death, migration, or invasion of the cancer cells.
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spelling pubmed-82267922021-06-26 Comparison of Transcriptomic Profiles of MiaPaCa-2 Pancreatic Cancer Cells Treated with Different Statins Rimpelová, Silvie Kolář, Michal Strnad, Hynek Ruml, Tomáš Vítek, Libor Gbelcová, Helena Molecules Article Statins have been widely used for the treatment of hypercholesterolemia due to their ability to inhibit HMG-CoA reductase, the rate-limiting enzyme of de novo cholesterol synthesis, via the so-called mevalonate pathway. However, their inhibitory action also causes depletion of downstream intermediates of the pathway, resulting in the pleiotropic effects of statins, including the beneficial impact in the treatment of cancer. In our study, we compared the effect of all eight existing statins on the expression of genes, the products of which are implicated in cancer inhibition and suggested the molecular mechanisms of their action in epigenetic and posttranslational regulation, and in cell-cycle arrest, death, migration, or invasion of the cancer cells. MDPI 2021-06-09 /pmc/articles/PMC8226792/ /pubmed/34207840 http://dx.doi.org/10.3390/molecules26123528 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Rimpelová, Silvie
Kolář, Michal
Strnad, Hynek
Ruml, Tomáš
Vítek, Libor
Gbelcová, Helena
Comparison of Transcriptomic Profiles of MiaPaCa-2 Pancreatic Cancer Cells Treated with Different Statins
title Comparison of Transcriptomic Profiles of MiaPaCa-2 Pancreatic Cancer Cells Treated with Different Statins
title_full Comparison of Transcriptomic Profiles of MiaPaCa-2 Pancreatic Cancer Cells Treated with Different Statins
title_fullStr Comparison of Transcriptomic Profiles of MiaPaCa-2 Pancreatic Cancer Cells Treated with Different Statins
title_full_unstemmed Comparison of Transcriptomic Profiles of MiaPaCa-2 Pancreatic Cancer Cells Treated with Different Statins
title_short Comparison of Transcriptomic Profiles of MiaPaCa-2 Pancreatic Cancer Cells Treated with Different Statins
title_sort comparison of transcriptomic profiles of miapaca-2 pancreatic cancer cells treated with different statins
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8226792/
https://www.ncbi.nlm.nih.gov/pubmed/34207840
http://dx.doi.org/10.3390/molecules26123528
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