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Deficiency in the 15 kDa Selenoprotein Inhibits Human Colon Cancer Cell Growth
Selenium is an essential micronutrient for humans and animals, and is thought to provide protection against some forms of cancer. These protective effects appear to be mediated, at least in part, through selenium-containing proteins (selenoproteins). Recent studies in a mouse colon cancer cell line...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3257736/ https://www.ncbi.nlm.nih.gov/pubmed/22254125 http://dx.doi.org/10.3390/nu3090805 |
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author | Tsuji, Petra A. Naranjo-Suarez, Salvador Carlson, Bradley A. Tobe, Ryuta Yoo, Min-Hyuk Davis, Cindy D. |
author_facet | Tsuji, Petra A. Naranjo-Suarez, Salvador Carlson, Bradley A. Tobe, Ryuta Yoo, Min-Hyuk Davis, Cindy D. |
author_sort | Tsuji, Petra A. |
collection | PubMed |
description | Selenium is an essential micronutrient for humans and animals, and is thought to provide protection against some forms of cancer. These protective effects appear to be mediated, at least in part, through selenium-containing proteins (selenoproteins). Recent studies in a mouse colon cancer cell line have shown that the 15 kDa selenoprotein (Sep15) may also play a role in promoting colon cancer. The current study investigated whether the effects of reversing the cancer phenotype observed when Sep15 was removed in mouse colon cancer cells, were recapitulated in HCT116 and HT29 human colorectal carcinoma cells. Targeted down-regulation of Sep15 using RNAi technology in these human colon cancer cell lines resulted in similarly decreased growth under anchorage-dependent and anchorage-independent conditions. However, the magnitude of reduction in cell growth was much less than in the mouse colon cancer cell line investigated previously. Furthermore, changes in cell cycle distribution were observed, indicating a delayed release of Sep15 deficient cells from the G(0)/G(1) phase after synchronization. The potential mechanism by which human colon cancer cells lacking Sep15 revert their cancer phenotype will need to be explored further. |
format | Online Article Text |
id | pubmed-3257736 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-32577362012-01-17 Deficiency in the 15 kDa Selenoprotein Inhibits Human Colon Cancer Cell Growth Tsuji, Petra A. Naranjo-Suarez, Salvador Carlson, Bradley A. Tobe, Ryuta Yoo, Min-Hyuk Davis, Cindy D. Nutrients Article Selenium is an essential micronutrient for humans and animals, and is thought to provide protection against some forms of cancer. These protective effects appear to be mediated, at least in part, through selenium-containing proteins (selenoproteins). Recent studies in a mouse colon cancer cell line have shown that the 15 kDa selenoprotein (Sep15) may also play a role in promoting colon cancer. The current study investigated whether the effects of reversing the cancer phenotype observed when Sep15 was removed in mouse colon cancer cells, were recapitulated in HCT116 and HT29 human colorectal carcinoma cells. Targeted down-regulation of Sep15 using RNAi technology in these human colon cancer cell lines resulted in similarly decreased growth under anchorage-dependent and anchorage-independent conditions. However, the magnitude of reduction in cell growth was much less than in the mouse colon cancer cell line investigated previously. Furthermore, changes in cell cycle distribution were observed, indicating a delayed release of Sep15 deficient cells from the G(0)/G(1) phase after synchronization. The potential mechanism by which human colon cancer cells lacking Sep15 revert their cancer phenotype will need to be explored further. MDPI 2011-09-05 /pmc/articles/PMC3257736/ /pubmed/22254125 http://dx.doi.org/10.3390/nu3090805 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Tsuji, Petra A. Naranjo-Suarez, Salvador Carlson, Bradley A. Tobe, Ryuta Yoo, Min-Hyuk Davis, Cindy D. Deficiency in the 15 kDa Selenoprotein Inhibits Human Colon Cancer Cell Growth |
title | Deficiency in the 15 kDa Selenoprotein Inhibits Human Colon Cancer Cell Growth |
title_full | Deficiency in the 15 kDa Selenoprotein Inhibits Human Colon Cancer Cell Growth |
title_fullStr | Deficiency in the 15 kDa Selenoprotein Inhibits Human Colon Cancer Cell Growth |
title_full_unstemmed | Deficiency in the 15 kDa Selenoprotein Inhibits Human Colon Cancer Cell Growth |
title_short | Deficiency in the 15 kDa Selenoprotein Inhibits Human Colon Cancer Cell Growth |
title_sort | deficiency in the 15 kda selenoprotein inhibits human colon cancer cell growth |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3257736/ https://www.ncbi.nlm.nih.gov/pubmed/22254125 http://dx.doi.org/10.3390/nu3090805 |
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