Cargando…
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...
Autores principales: | , , , , , , |
---|---|
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 |
_version_ | 1782134073555156992 |
---|---|
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. |
format | Text |
id | pubmed-1913536 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT jungmonika insearchofsuitablereferencegenesforgeneexpressionstudiesofhumanrenalcellcarcinomabyrealtimepcr AT ramankulovazizbek insearchofsuitablereferencegenesforgeneexpressionstudiesofhumanrenalcellcarcinomabyrealtimepcr AT roigasjan insearchofsuitablereferencegenesforgeneexpressionstudiesofhumanrenalcellcarcinomabyrealtimepcr AT johannsenmanfred insearchofsuitablereferencegenesforgeneexpressionstudiesofhumanrenalcellcarcinomabyrealtimepcr AT ringsdorfmartin insearchofsuitablereferencegenesforgeneexpressionstudiesofhumanrenalcellcarcinomabyrealtimepcr AT kristiansenglen insearchofsuitablereferencegenesforgeneexpressionstudiesofhumanrenalcellcarcinomabyrealtimepcr AT jungklaus insearchofsuitablereferencegenesforgeneexpressionstudiesofhumanrenalcellcarcinomabyrealtimepcr |