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Time-Qualified Patterns of Variation of PPARγ, DNMT1, and DNMT3B Expression in Pancreatic Cancer Cell Lines

Carcinogenesis is related to the loss of homeostatic control of cellular processes regulated by transcriptional circuits and epigenetic mechanisms. Among these, the activities of peroxisome proliferator-activated receptors (PPARs) and DNA methyltransferases (DNMTs) are crucial and intertwined. PPARγ...

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Autores principales: Pazienza, Valerio, Tavano, Francesca, Francavilla, Massimo, Fontana, Andrea, Pellegrini, Fabio, Benegiamo, Giorgia, Corbo, Vincenzo, di Mola, Fabio Francesco, Di Sebastiano, Pierluigi, Andriulli, Angelo, Mazzoccoli, Gianluigi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3433147/
https://www.ncbi.nlm.nih.gov/pubmed/22966223
http://dx.doi.org/10.1155/2012/890875
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author Pazienza, Valerio
Tavano, Francesca
Francavilla, Massimo
Fontana, Andrea
Pellegrini, Fabio
Benegiamo, Giorgia
Corbo, Vincenzo
di Mola, Fabio Francesco
Di Sebastiano, Pierluigi
Andriulli, Angelo
Mazzoccoli, Gianluigi
author_facet Pazienza, Valerio
Tavano, Francesca
Francavilla, Massimo
Fontana, Andrea
Pellegrini, Fabio
Benegiamo, Giorgia
Corbo, Vincenzo
di Mola, Fabio Francesco
Di Sebastiano, Pierluigi
Andriulli, Angelo
Mazzoccoli, Gianluigi
author_sort Pazienza, Valerio
collection PubMed
description Carcinogenesis is related to the loss of homeostatic control of cellular processes regulated by transcriptional circuits and epigenetic mechanisms. Among these, the activities of peroxisome proliferator-activated receptors (PPARs) and DNA methyltransferases (DNMTs) are crucial and intertwined. PPARγ is a key regulator of cell fate, linking nutrient sensing to transcription processes, and its expression oscillates with circadian rhythmicity. Aim of our study was to assess the periodicity of PPARγ and DNMTs in pancreatic cancer (PC). We investigated the time-related patterns of PPARG, DNMT1, and DNMT3B expression monitoring their mRNA levels by qRT-PCR at different time points over a 28-hour span in BxPC-3, CFPAC-1, PANC-1, and MIAPaCa-2 PC cells after synchronization with serum shock. PPARG and DNMT1 expression in PANC-1 cells and PPARG expression in MIAPaCa-2 cells were characterized by a 24 h period oscillation, and a borderline significant rhythm was observed for the PPARG, DNMT1, and DNMT3B expression profiles in the other cell lines. The time-qualified profiles of gene expression showed different shapes and phase relationships in the PC cell lines examined. In conclusion, PPARG and DNMTs expression is characterized by different time-qualified patterns in cell lines derived from human PC, and this heterogeneity could influence cell phenotype and human disease behaviour.
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spelling pubmed-34331472012-09-10 Time-Qualified Patterns of Variation of PPARγ, DNMT1, and DNMT3B Expression in Pancreatic Cancer Cell Lines Pazienza, Valerio Tavano, Francesca Francavilla, Massimo Fontana, Andrea Pellegrini, Fabio Benegiamo, Giorgia Corbo, Vincenzo di Mola, Fabio Francesco Di Sebastiano, Pierluigi Andriulli, Angelo Mazzoccoli, Gianluigi PPAR Res Research Article Carcinogenesis is related to the loss of homeostatic control of cellular processes regulated by transcriptional circuits and epigenetic mechanisms. Among these, the activities of peroxisome proliferator-activated receptors (PPARs) and DNA methyltransferases (DNMTs) are crucial and intertwined. PPARγ is a key regulator of cell fate, linking nutrient sensing to transcription processes, and its expression oscillates with circadian rhythmicity. Aim of our study was to assess the periodicity of PPARγ and DNMTs in pancreatic cancer (PC). We investigated the time-related patterns of PPARG, DNMT1, and DNMT3B expression monitoring their mRNA levels by qRT-PCR at different time points over a 28-hour span in BxPC-3, CFPAC-1, PANC-1, and MIAPaCa-2 PC cells after synchronization with serum shock. PPARG and DNMT1 expression in PANC-1 cells and PPARG expression in MIAPaCa-2 cells were characterized by a 24 h period oscillation, and a borderline significant rhythm was observed for the PPARG, DNMT1, and DNMT3B expression profiles in the other cell lines. The time-qualified profiles of gene expression showed different shapes and phase relationships in the PC cell lines examined. In conclusion, PPARG and DNMTs expression is characterized by different time-qualified patterns in cell lines derived from human PC, and this heterogeneity could influence cell phenotype and human disease behaviour. Hindawi Publishing Corporation 2012 2012-08-26 /pmc/articles/PMC3433147/ /pubmed/22966223 http://dx.doi.org/10.1155/2012/890875 Text en Copyright © 2012 Valerio Pazienza et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Pazienza, Valerio
Tavano, Francesca
Francavilla, Massimo
Fontana, Andrea
Pellegrini, Fabio
Benegiamo, Giorgia
Corbo, Vincenzo
di Mola, Fabio Francesco
Di Sebastiano, Pierluigi
Andriulli, Angelo
Mazzoccoli, Gianluigi
Time-Qualified Patterns of Variation of PPARγ, DNMT1, and DNMT3B Expression in Pancreatic Cancer Cell Lines
title Time-Qualified Patterns of Variation of PPARγ, DNMT1, and DNMT3B Expression in Pancreatic Cancer Cell Lines
title_full Time-Qualified Patterns of Variation of PPARγ, DNMT1, and DNMT3B Expression in Pancreatic Cancer Cell Lines
title_fullStr Time-Qualified Patterns of Variation of PPARγ, DNMT1, and DNMT3B Expression in Pancreatic Cancer Cell Lines
title_full_unstemmed Time-Qualified Patterns of Variation of PPARγ, DNMT1, and DNMT3B Expression in Pancreatic Cancer Cell Lines
title_short Time-Qualified Patterns of Variation of PPARγ, DNMT1, and DNMT3B Expression in Pancreatic Cancer Cell Lines
title_sort time-qualified patterns of variation of pparγ, dnmt1, and dnmt3b expression in pancreatic cancer cell lines
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3433147/
https://www.ncbi.nlm.nih.gov/pubmed/22966223
http://dx.doi.org/10.1155/2012/890875
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