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Placenta-specific novel splice variants of Rho GDP dissociation inhibitor β are highly expressed in cancerous cells
BACKGROUND: Alternative splicing of pre-mRNA transcripts not only plays a role in normal molecular processes but is also associated with cancer development. While normal transcripts are ubiquitously expressed in normal tissues, splice variants created through abnormal alternative splicing events are...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3554444/ https://www.ncbi.nlm.nih.gov/pubmed/23206989 http://dx.doi.org/10.1186/1756-0500-5-666 |
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author | Hatakeyama, Keiichi Fukuda, Yorikane Ohshima, Keiichi Terashima, Masanori Yamaguchi, Ken Mochizuki, Tohru |
author_facet | Hatakeyama, Keiichi Fukuda, Yorikane Ohshima, Keiichi Terashima, Masanori Yamaguchi, Ken Mochizuki, Tohru |
author_sort | Hatakeyama, Keiichi |
collection | PubMed |
description | BACKGROUND: Alternative splicing of pre-mRNA transcripts not only plays a role in normal molecular processes but is also associated with cancer development. While normal transcripts are ubiquitously expressed in normal tissues, splice variants created through abnormal alternative splicing events are often expressed in cancer cells. Although the Rho GDP dissociation inhibitor β (ARHGDIB) gene has been found to be ubiquitously expressed in normal tissues and involved in cancer development, the presence of splice variants of ARHGDIB has not yet been investigated. RESULTS: Validation analysis for the presence of and exon structures of splice variants of ARHGDIB, performed using reverse-transcriptase polymerase chain reaction and DNA sequencing, successfully identified novel splice variants of ARHGDIB, that is, 6a, 6b, and 6c, in colon, pancreas, stomach, and breast cancer cell lines. Quantitative real-time polymerase chain reaction analysis showed that these variants were also highly expressed in normal placental tissue but not in other types of normal tissue. CONCLUSIONS: Expression of ARHGDIB variants 6a, 6b, and 6c appears to be restricted to cancer cells and normal placental tissue, suggesting that these variants possess cancer-specific functions and, as such, are potential cancer-related biomarkers. |
format | Online Article Text |
id | pubmed-3554444 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35544442013-01-29 Placenta-specific novel splice variants of Rho GDP dissociation inhibitor β are highly expressed in cancerous cells Hatakeyama, Keiichi Fukuda, Yorikane Ohshima, Keiichi Terashima, Masanori Yamaguchi, Ken Mochizuki, Tohru BMC Res Notes Research Article BACKGROUND: Alternative splicing of pre-mRNA transcripts not only plays a role in normal molecular processes but is also associated with cancer development. While normal transcripts are ubiquitously expressed in normal tissues, splice variants created through abnormal alternative splicing events are often expressed in cancer cells. Although the Rho GDP dissociation inhibitor β (ARHGDIB) gene has been found to be ubiquitously expressed in normal tissues and involved in cancer development, the presence of splice variants of ARHGDIB has not yet been investigated. RESULTS: Validation analysis for the presence of and exon structures of splice variants of ARHGDIB, performed using reverse-transcriptase polymerase chain reaction and DNA sequencing, successfully identified novel splice variants of ARHGDIB, that is, 6a, 6b, and 6c, in colon, pancreas, stomach, and breast cancer cell lines. Quantitative real-time polymerase chain reaction analysis showed that these variants were also highly expressed in normal placental tissue but not in other types of normal tissue. CONCLUSIONS: Expression of ARHGDIB variants 6a, 6b, and 6c appears to be restricted to cancer cells and normal placental tissue, suggesting that these variants possess cancer-specific functions and, as such, are potential cancer-related biomarkers. BioMed Central 2012-12-03 /pmc/articles/PMC3554444/ /pubmed/23206989 http://dx.doi.org/10.1186/1756-0500-5-666 Text en Copyright ©2012 Hatakeyama et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Hatakeyama, Keiichi Fukuda, Yorikane Ohshima, Keiichi Terashima, Masanori Yamaguchi, Ken Mochizuki, Tohru Placenta-specific novel splice variants of Rho GDP dissociation inhibitor β are highly expressed in cancerous cells |
title | Placenta-specific novel splice variants of Rho GDP dissociation inhibitor β are highly expressed in cancerous cells |
title_full | Placenta-specific novel splice variants of Rho GDP dissociation inhibitor β are highly expressed in cancerous cells |
title_fullStr | Placenta-specific novel splice variants of Rho GDP dissociation inhibitor β are highly expressed in cancerous cells |
title_full_unstemmed | Placenta-specific novel splice variants of Rho GDP dissociation inhibitor β are highly expressed in cancerous cells |
title_short | Placenta-specific novel splice variants of Rho GDP dissociation inhibitor β are highly expressed in cancerous cells |
title_sort | placenta-specific novel splice variants of rho gdp dissociation inhibitor β are highly expressed in cancerous cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3554444/ https://www.ncbi.nlm.nih.gov/pubmed/23206989 http://dx.doi.org/10.1186/1756-0500-5-666 |
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