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Expression profiling of colorectal cancer cells reveals inhibition of DNA replication licensing by extracellular calcium()

Colorectal cancer is one of the most common cancers in industrialised societies. Epidemiological studies, animal experiments, and randomized clinical trials have shown that dietary factors can influence all stages of colorectal carcinogenesis, from initiation through promotion to progression. Calciu...

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Autores principales: Aggarwal, Abhishek, Schulz, Herbert, Manhardt, Teresa, Bilban, Martin, Thakker, Rajesh V, Kallay, Enikö
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Pub. Co 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5424886/
https://www.ncbi.nlm.nih.gov/pubmed/28161520
http://dx.doi.org/10.1016/j.bbamcr.2017.01.017
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author Aggarwal, Abhishek
Schulz, Herbert
Manhardt, Teresa
Bilban, Martin
Thakker, Rajesh V
Kallay, Enikö
author_facet Aggarwal, Abhishek
Schulz, Herbert
Manhardt, Teresa
Bilban, Martin
Thakker, Rajesh V
Kallay, Enikö
author_sort Aggarwal, Abhishek
collection PubMed
description Colorectal cancer is one of the most common cancers in industrialised societies. Epidemiological studies, animal experiments, and randomized clinical trials have shown that dietary factors can influence all stages of colorectal carcinogenesis, from initiation through promotion to progression. Calcium is one of the factors with a chemoprophylactic effect in colorectal cancer. The aim of this study was to understand the molecular mechanisms of the anti-tumorigenic effects of extracellular calcium ([Ca(2+)](o)) in colon cancer cells. Gene expression microarray analysis of colon cancer cells treated for 1, 4, and 24 h with 2 mM [Ca(2+)](o) identified significant changes in expression of 1571 probe sets (ANOVA, p < 10(− 5)). The main biological processes affected by [Ca(2+)](o) were DNA replication, cell division, and regulation of transcription. All factors involved in DNA replication-licensing were significantly downregulated by [Ca(2+)](o). Furthermore, we show that the calcium-sensing receptor (CaSR), a G protein-coupled receptor is a mediator involved in this process. To test whether these results were physiologically relevant, we fed mice with a standard diet containing low (0.04%), intermediate (0.1%), or high (0.9%) levels of dietary calcium. The main molecules regulating replication licensing were inhibited also in vivo, in the colon of mice fed high calcium diet. We show that among the mechanisms behind the chemopreventive effect of [Ca(2+)](o) is inhibition of replication licensing, a process often deregulated in neoplastic transformation. Our data suggest that dietary calcium is effective in preventing replicative stress, one of the main drivers of cancer and this process is mediated by the calcium-sensing receptor.
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spelling pubmed-54248862017-06-01 Expression profiling of colorectal cancer cells reveals inhibition of DNA replication licensing by extracellular calcium() Aggarwal, Abhishek Schulz, Herbert Manhardt, Teresa Bilban, Martin Thakker, Rajesh V Kallay, Enikö Biochim Biophys Acta Article Colorectal cancer is one of the most common cancers in industrialised societies. Epidemiological studies, animal experiments, and randomized clinical trials have shown that dietary factors can influence all stages of colorectal carcinogenesis, from initiation through promotion to progression. Calcium is one of the factors with a chemoprophylactic effect in colorectal cancer. The aim of this study was to understand the molecular mechanisms of the anti-tumorigenic effects of extracellular calcium ([Ca(2+)](o)) in colon cancer cells. Gene expression microarray analysis of colon cancer cells treated for 1, 4, and 24 h with 2 mM [Ca(2+)](o) identified significant changes in expression of 1571 probe sets (ANOVA, p < 10(− 5)). The main biological processes affected by [Ca(2+)](o) were DNA replication, cell division, and regulation of transcription. All factors involved in DNA replication-licensing were significantly downregulated by [Ca(2+)](o). Furthermore, we show that the calcium-sensing receptor (CaSR), a G protein-coupled receptor is a mediator involved in this process. To test whether these results were physiologically relevant, we fed mice with a standard diet containing low (0.04%), intermediate (0.1%), or high (0.9%) levels of dietary calcium. The main molecules regulating replication licensing were inhibited also in vivo, in the colon of mice fed high calcium diet. We show that among the mechanisms behind the chemopreventive effect of [Ca(2+)](o) is inhibition of replication licensing, a process often deregulated in neoplastic transformation. Our data suggest that dietary calcium is effective in preventing replicative stress, one of the main drivers of cancer and this process is mediated by the calcium-sensing receptor. Elsevier Pub. Co 2017-06 /pmc/articles/PMC5424886/ /pubmed/28161520 http://dx.doi.org/10.1016/j.bbamcr.2017.01.017 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Aggarwal, Abhishek
Schulz, Herbert
Manhardt, Teresa
Bilban, Martin
Thakker, Rajesh V
Kallay, Enikö
Expression profiling of colorectal cancer cells reveals inhibition of DNA replication licensing by extracellular calcium()
title Expression profiling of colorectal cancer cells reveals inhibition of DNA replication licensing by extracellular calcium()
title_full Expression profiling of colorectal cancer cells reveals inhibition of DNA replication licensing by extracellular calcium()
title_fullStr Expression profiling of colorectal cancer cells reveals inhibition of DNA replication licensing by extracellular calcium()
title_full_unstemmed Expression profiling of colorectal cancer cells reveals inhibition of DNA replication licensing by extracellular calcium()
title_short Expression profiling of colorectal cancer cells reveals inhibition of DNA replication licensing by extracellular calcium()
title_sort expression profiling of colorectal cancer cells reveals inhibition of dna replication licensing by extracellular calcium()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5424886/
https://www.ncbi.nlm.nih.gov/pubmed/28161520
http://dx.doi.org/10.1016/j.bbamcr.2017.01.017
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