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A gastrin transcript expressed in gastrointestinal cancer cells contains an internal ribosome entry site
As the hormone gastrin promotes gastrointestinal (GI) cancer progression by triggering survival pathways, regulation of gastrin expression at the translational level was explored. Sequence within the 5′ untranslated region of a gastrin transcript expressed in GI cancer cells was investigated, then c...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2391123/ https://www.ncbi.nlm.nih.gov/pubmed/18392051 http://dx.doi.org/10.1038/sj.bjc.6604326 |
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author | Grabowska, A M Berry, C A Hughes, J Bushell, M Willis, A E Watson, S A |
author_facet | Grabowska, A M Berry, C A Hughes, J Bushell, M Willis, A E Watson, S A |
author_sort | Grabowska, A M |
collection | PubMed |
description | As the hormone gastrin promotes gastrointestinal (GI) cancer progression by triggering survival pathways, regulation of gastrin expression at the translational level was explored. Sequence within the 5′ untranslated region of a gastrin transcript expressed in GI cancer cells was investigated, then cloned into a bicistronic vector upstream of firefly luciferase and transfected into a series of GI cancer cell lines. Firefly luciferase activity was measured relative to that of a cap-dependent Renilla luciferase. A gastrin transcript that was different from that described in Ensembl was expressed in GI cancer cells. Its transcription appears to be initiated within the region designated as the gene's first intron. In GI cancer cells transfected with the bicistronic construct, firefly luciferase activity increased 8–15-fold compared with the control vector, and there was a further induction of the signal (up to 25-fold) following exposure of the cells to genotoxic stress or hypoxia, suggesting that the sequence acts as an internal ribosome entry site. These data suggest that the gastrin transcript within GI cancer cells contains an internal ribosome entry site that may allow continued expression of gastrin peptides when normal translational mechanisms are inactive, such as in hypoxia, thereby promoting cancer cell survival. |
format | Text |
id | pubmed-2391123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23911232009-09-10 A gastrin transcript expressed in gastrointestinal cancer cells contains an internal ribosome entry site Grabowska, A M Berry, C A Hughes, J Bushell, M Willis, A E Watson, S A Br J Cancer Genetics and Genomics As the hormone gastrin promotes gastrointestinal (GI) cancer progression by triggering survival pathways, regulation of gastrin expression at the translational level was explored. Sequence within the 5′ untranslated region of a gastrin transcript expressed in GI cancer cells was investigated, then cloned into a bicistronic vector upstream of firefly luciferase and transfected into a series of GI cancer cell lines. Firefly luciferase activity was measured relative to that of a cap-dependent Renilla luciferase. A gastrin transcript that was different from that described in Ensembl was expressed in GI cancer cells. Its transcription appears to be initiated within the region designated as the gene's first intron. In GI cancer cells transfected with the bicistronic construct, firefly luciferase activity increased 8–15-fold compared with the control vector, and there was a further induction of the signal (up to 25-fold) following exposure of the cells to genotoxic stress or hypoxia, suggesting that the sequence acts as an internal ribosome entry site. These data suggest that the gastrin transcript within GI cancer cells contains an internal ribosome entry site that may allow continued expression of gastrin peptides when normal translational mechanisms are inactive, such as in hypoxia, thereby promoting cancer cell survival. Nature Publishing Group 2008-05-20 2008-04-08 /pmc/articles/PMC2391123/ /pubmed/18392051 http://dx.doi.org/10.1038/sj.bjc.6604326 Text en Copyright © 2008 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Genetics and Genomics Grabowska, A M Berry, C A Hughes, J Bushell, M Willis, A E Watson, S A A gastrin transcript expressed in gastrointestinal cancer cells contains an internal ribosome entry site |
title | A gastrin transcript expressed in gastrointestinal cancer cells contains an internal ribosome entry site |
title_full | A gastrin transcript expressed in gastrointestinal cancer cells contains an internal ribosome entry site |
title_fullStr | A gastrin transcript expressed in gastrointestinal cancer cells contains an internal ribosome entry site |
title_full_unstemmed | A gastrin transcript expressed in gastrointestinal cancer cells contains an internal ribosome entry site |
title_short | A gastrin transcript expressed in gastrointestinal cancer cells contains an internal ribosome entry site |
title_sort | gastrin transcript expressed in gastrointestinal cancer cells contains an internal ribosome entry site |
topic | Genetics and Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2391123/ https://www.ncbi.nlm.nih.gov/pubmed/18392051 http://dx.doi.org/10.1038/sj.bjc.6604326 |
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