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Open Access Highly Accessed Research article

Suitable reference genes for real-time PCR in human HBV-related hepatocellular carcinoma with different clinical prognoses

Li-Yun Fu12, Hu-Liang Jia1, Qiong-Zhu Dong12, Jin-Cai Wu1, Yue Zhao12, Hai-Jun Zhou1, Ning Ren1, Qin-Hai Ye1 and Lun-Xiu Qin12*

Author Affiliations

1 Liver Cancer Institute and Zhongshan Hospital, Fudan University, Shanghai, PR China

2 Research Center for Cancer, Institutes of Biomedical Sciences, Fudan University, Shanghai, PR China

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BMC Cancer 2009, 9:49  doi:10.1186/1471-2407-9-49

Published: 6 February 2009

Abstract

Background

Housekeeping genes are routinely used as endogenous references to account for experimental differences in gene expression assays. However, recent reports show that they could be de-regulated in different diseases, model animals, or even under varied experimental conditions, which may lead to unreliable results and consequently misinterpretations. This study focused on the selection of suitable reference genes for quantitative PCR in human hepatitis B virus (HBV)-related hepatocellular carcinoma (HCC) with different clinical outcomes.

Methods

We evaluated 6 commonly used housekeeping genes' expression levels in 108 HBV-related HCCs' matched tumor and non-tomor tissue samples with different clinical outcomes and 26 normal liver specimens by real-time PCR. The expression stability of the 6 genes was compared using the software programs geNorm and NormFinder. To show the impact of reference genes on data analysis, we took PGK1 as a target gene normalized by each reference gene, and performed one-way ANOVA and the equivalence test.

Results

With the geNorm and NormFinder software programs, analysis of TBP and HPRT1 showed the best stability in all tissue samples, while 18s and ACTB were less stable. When 18s or ACTB was used for normalization, no significant difference of PGK1 expression (p > 0.05) was found among HCC tissues with and without metastasis, and normal liver specimens; however, dramatically differences (p < 0.001) were observed when either TBP or the combination of TBP and HPRT1 were selected as reference genes.

Conclusion

TBP and HPRT1 are the most reliable reference genes for q-PCR normalization in HBV-related HCC specimens. However, the well-used ACTB and 18S are not suitable, which actually lead to the misinterpretation of the results in gene expression analysis.