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A study demonstrating the suitability of the two housekeeping genes PPIA and …


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

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

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

Monika Jung1, Azizbek Ramankulov,3, Jan Roigas1, Manfred Johannsen1, Martin Ringsdorf1, Glen Kristiansen2 and Klaus Jung1

1Department of Urology, Charité – Universitätsmedizin Berlin, Campus Charité Mitte, Charitéplatz 1, 10117 Berlin, Germany
2Institute of Pathology, Charité – Universitätsmedizin Berlin, Campus Charité Mitte, Charitéplatz 1, 10117 Berlin, Germany
3Republic Center of Urology, Bishkek, Kyrgyz Republic

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.

 



BMC Molecular Biology 2007, 8:47. This is an Open Access article distributed under the terms of the Creative Commons Attribution License.

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