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In search of suitable reference genes for gene expression studies of human renal cell carcinoma by real-time PCR

BACKGROUND: Housekeeping genes are commonly used as endogenous reference genes for the relative quantification of target genes in gene expression studies. No conclusive systematic study comparing the suitability of different candidate reference genes in clear cell renal cell carcinoma has been publi...

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Autores principales: Jung, Monika, Ramankulov, Azizbek, Roigas, Jan, Johannsen, Manfred, Ringsdorf, Martin, Kristiansen, Glen, Jung, Klaus
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1913536/
https://www.ncbi.nlm.nih.gov/pubmed/17559644
http://dx.doi.org/10.1186/1471-2199-8-47
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author Jung, Monika
Ramankulov, Azizbek
Roigas, Jan
Johannsen, Manfred
Ringsdorf, Martin
Kristiansen, Glen
Jung, Klaus
author_facet Jung, Monika
Ramankulov, Azizbek
Roigas, Jan
Johannsen, Manfred
Ringsdorf, Martin
Kristiansen, Glen
Jung, Klaus
author_sort Jung, Monika
collection PubMed
description BACKGROUND: Housekeeping genes are commonly used as endogenous reference genes for the relative quantification of target genes in gene expression studies. No conclusive systematic study comparing the suitability of different candidate reference genes in clear cell renal cell carcinoma has been published to date. To remedy this situation, 10 housekeeping genes for normalizing purposes of RT-PCR measurements already recommended in various studies were examined with regard to their usefulness as reference genes. RESULTS: The expression of the potential reference genes was examined in matched malignant and non-malignant tissue specimens from 25 patients with clear cell renal cell carcinoma. Quality assessment of isolated RNA performed with a 2100 Agilent Bioanalyzer showed a mean RNA integrity number of 8.7 for all samples. The between-run variations related to the crossing points of PCR reactions of a control material ranged from 0.17% to 0.38%. The expression of all genes did not depend on age, sex, and tumour stage. Except the genes TATA box binding protein (TBP) and peptidylprolyl isomerase A (PPIA), all genes showed significant differences in expression between malignant and non-malignant pairs. The expression stability of the candidate reference genes was additionally controlled using the software programs geNorm and NormFinder. TBP and PPIA were validated as suitable reference genes by normalizing the target gene ADAM9 using these two most stably expressed genes in comparison with up- and down-regulated housekeeping genes of the panel. CONCLUSION: Our study demonstrated the suitability of the two housekeeping genes PPIA and TBP as endogenous reference genes when comparing malignant tissue samples with adjacent normal tissue samples from clear cell renal cell carcinoma. Both genes are recommended as reference genes for relative gene quantification in gene profiling studies either as single gene or preferably in combination.
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spelling pubmed-19135362007-07-10 In search of suitable reference genes for gene expression studies of human renal cell carcinoma by real-time PCR Jung, Monika Ramankulov, Azizbek Roigas, Jan Johannsen, Manfred Ringsdorf, Martin Kristiansen, Glen Jung, Klaus BMC Mol Biol Research Article BACKGROUND: Housekeeping genes are commonly used as endogenous reference genes for the relative quantification of target genes in gene expression studies. No conclusive systematic study comparing the suitability of different candidate reference genes in clear cell renal cell carcinoma has been published to date. To remedy this situation, 10 housekeeping genes for normalizing purposes of RT-PCR measurements already recommended in various studies were examined with regard to their usefulness as reference genes. RESULTS: The expression of the potential reference genes was examined in matched malignant and non-malignant tissue specimens from 25 patients with clear cell renal cell carcinoma. Quality assessment of isolated RNA performed with a 2100 Agilent Bioanalyzer showed a mean RNA integrity number of 8.7 for all samples. The between-run variations related to the crossing points of PCR reactions of a control material ranged from 0.17% to 0.38%. The expression of all genes did not depend on age, sex, and tumour stage. Except the genes TATA box binding protein (TBP) and peptidylprolyl isomerase A (PPIA), all genes showed significant differences in expression between malignant and non-malignant pairs. The expression stability of the candidate reference genes was additionally controlled using the software programs geNorm and NormFinder. TBP and PPIA were validated as suitable reference genes by normalizing the target gene ADAM9 using these two most stably expressed genes in comparison with up- and down-regulated housekeeping genes of the panel. CONCLUSION: Our study demonstrated the suitability of the two housekeeping genes PPIA and TBP as endogenous reference genes when comparing malignant tissue samples with adjacent normal tissue samples from clear cell renal cell carcinoma. Both genes are recommended as reference genes for relative gene quantification in gene profiling studies either as single gene or preferably in combination. BioMed Central 2007-06-08 /pmc/articles/PMC1913536/ /pubmed/17559644 http://dx.doi.org/10.1186/1471-2199-8-47 Text en Copyright © 2007 Jung 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
Jung, Monika
Ramankulov, Azizbek
Roigas, Jan
Johannsen, Manfred
Ringsdorf, Martin
Kristiansen, Glen
Jung, Klaus
In search of suitable reference genes for gene expression studies of human renal cell carcinoma by real-time PCR
title In search of suitable reference genes for gene expression studies of human renal cell carcinoma by real-time PCR
title_full In search of suitable reference genes for gene expression studies of human renal cell carcinoma by real-time PCR
title_fullStr In search of suitable reference genes for gene expression studies of human renal cell carcinoma by real-time PCR
title_full_unstemmed In search of suitable reference genes for gene expression studies of human renal cell carcinoma by real-time PCR
title_short In search of suitable reference genes for gene expression studies of human renal cell carcinoma by real-time PCR
title_sort in search of suitable reference genes for gene expression studies of human renal cell carcinoma by real-time pcr
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1913536/
https://www.ncbi.nlm.nih.gov/pubmed/17559644
http://dx.doi.org/10.1186/1471-2199-8-47
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