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RASSF1C modulates the expression of a stem cell renewal gene, PIWIL1

BACKGROUND: RASSF1A and RASSF1C are two major isoforms encoded by the Ras association domain family 1 (RASSF1) gene through alternative promoter selection and mRNA splicing. RASSF1A is a well established tumor suppressor gene. Unlike RASSF1A, RASSF1C appears to have growth promoting actions in lung...

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Autores principales: Reeves, Mark E, Baldwin, Melissa L, Aragon, Robert, Baldwin, Scott, Chen, Shin-Tai, Li, Xinmin, Mohan, Subburaman, Amaar, Yousef G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3512503/
https://www.ncbi.nlm.nih.gov/pubmed/22591718
http://dx.doi.org/10.1186/1756-0500-5-239
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author Reeves, Mark E
Baldwin, Melissa L
Aragon, Robert
Baldwin, Scott
Chen, Shin-Tai
Li, Xinmin
Mohan, Subburaman
Amaar, Yousef G
author_facet Reeves, Mark E
Baldwin, Melissa L
Aragon, Robert
Baldwin, Scott
Chen, Shin-Tai
Li, Xinmin
Mohan, Subburaman
Amaar, Yousef G
author_sort Reeves, Mark E
collection PubMed
description BACKGROUND: RASSF1A and RASSF1C are two major isoforms encoded by the Ras association domain family 1 (RASSF1) gene through alternative promoter selection and mRNA splicing. RASSF1A is a well established tumor suppressor gene. Unlike RASSF1A, RASSF1C appears to have growth promoting actions in lung cancer. In this article, we report on the identification of novel RASSF1C target genes in non small cell lung cancer (NSCLC). METHODS: Over-expression and siRNA techniques were used to alter RASSF1C expression in human lung cancer cells, and Affymetrix-microarray study was conducted using NCI-H1299 cells over-expressing RASSF1C to identify RASSF1C target genes. RESULTS: The microarray study intriguingly shows that RASSF1C modulates the expression of a number of genes that are involved in cancer development, cell growth and proliferation, cell death, and cell cycle. We have validated the expression of some target genes using qRT-PCR. We demonstrate that RASSF1C over-expression increases, and silencing of RASSF1C decreases, the expression of PIWIL1 gene in NSCLC cells using qRT-PCR, immunostaining, and Western blot analysis. We also show that RASSF1C over-expression induces phosphorylation of ERK1/2 in lung cancer cells, and inhibition of the MEK-ERK1/2 pathway suppresses the expression of PIWIL1 gene expression, suggesting that RASSF1C may exert its activities on some target genes such as PIWIL1 through the activation of the MEK-ERK1/2 pathway. Also, PIWIL1 expression is elevated in lung cancer cell lines compared to normal lung epithelial cells. CONCLUSIONS: Taken together, our findings provide significant data to propose a model for investigating the role of RASSF1C/PIWIL1 proteins in initiation and progression of lung cancer.
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spelling pubmed-35125032012-12-04 RASSF1C modulates the expression of a stem cell renewal gene, PIWIL1 Reeves, Mark E Baldwin, Melissa L Aragon, Robert Baldwin, Scott Chen, Shin-Tai Li, Xinmin Mohan, Subburaman Amaar, Yousef G BMC Res Notes Research Article BACKGROUND: RASSF1A and RASSF1C are two major isoforms encoded by the Ras association domain family 1 (RASSF1) gene through alternative promoter selection and mRNA splicing. RASSF1A is a well established tumor suppressor gene. Unlike RASSF1A, RASSF1C appears to have growth promoting actions in lung cancer. In this article, we report on the identification of novel RASSF1C target genes in non small cell lung cancer (NSCLC). METHODS: Over-expression and siRNA techniques were used to alter RASSF1C expression in human lung cancer cells, and Affymetrix-microarray study was conducted using NCI-H1299 cells over-expressing RASSF1C to identify RASSF1C target genes. RESULTS: The microarray study intriguingly shows that RASSF1C modulates the expression of a number of genes that are involved in cancer development, cell growth and proliferation, cell death, and cell cycle. We have validated the expression of some target genes using qRT-PCR. We demonstrate that RASSF1C over-expression increases, and silencing of RASSF1C decreases, the expression of PIWIL1 gene in NSCLC cells using qRT-PCR, immunostaining, and Western blot analysis. We also show that RASSF1C over-expression induces phosphorylation of ERK1/2 in lung cancer cells, and inhibition of the MEK-ERK1/2 pathway suppresses the expression of PIWIL1 gene expression, suggesting that RASSF1C may exert its activities on some target genes such as PIWIL1 through the activation of the MEK-ERK1/2 pathway. Also, PIWIL1 expression is elevated in lung cancer cell lines compared to normal lung epithelial cells. CONCLUSIONS: Taken together, our findings provide significant data to propose a model for investigating the role of RASSF1C/PIWIL1 proteins in initiation and progression of lung cancer. BioMed Central 2012-05-16 /pmc/articles/PMC3512503/ /pubmed/22591718 http://dx.doi.org/10.1186/1756-0500-5-239 Text en Copyright ©2012 Reeves 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
Reeves, Mark E
Baldwin, Melissa L
Aragon, Robert
Baldwin, Scott
Chen, Shin-Tai
Li, Xinmin
Mohan, Subburaman
Amaar, Yousef G
RASSF1C modulates the expression of a stem cell renewal gene, PIWIL1
title RASSF1C modulates the expression of a stem cell renewal gene, PIWIL1
title_full RASSF1C modulates the expression of a stem cell renewal gene, PIWIL1
title_fullStr RASSF1C modulates the expression of a stem cell renewal gene, PIWIL1
title_full_unstemmed RASSF1C modulates the expression of a stem cell renewal gene, PIWIL1
title_short RASSF1C modulates the expression of a stem cell renewal gene, PIWIL1
title_sort rassf1c modulates the expression of a stem cell renewal gene, piwil1
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3512503/
https://www.ncbi.nlm.nih.gov/pubmed/22591718
http://dx.doi.org/10.1186/1756-0500-5-239
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