Nguewa Paul A, Agorreta Jackeline, Blanco David, Lozano Maria Dolores, Gomez-Roman Javier, Sanchez Blas A, Valles Iñaki, Pajares Maria J, Pio Ruben, Rodriguez Maria Jose, Montuenga Luis M, Calvo Alfonso
Division of Oncology, Center for Applied Medical Research (CIMA), University of Navarra, Avda, Pio XII, 55, 31008 Pamplona, Spain.
BMC Mol Biol. 2008 Nov 17;9:103. doi: 10.1186/1471-2199-9-103.
The accurate normalization of differentially expressed genes in lung cancer is essential for the identification of novel therapeutic targets and biomarkers by real time RT-PCR and microarrays. Although classical "housekeeping" genes, such as GAPDH, HPRT1, and beta-actin have been widely used in the past, their accuracy as reference genes for lung tissues has not been proven.
We have conducted a thorough analysis of a panel of 16 candidate reference genes for lung specimens and lung cell lines. Gene expression was measured by quantitative real time RT-PCR and expression stability was analyzed with the softwares GeNorm and NormFinder, mean of |Delta Ct| (= |Ct Normal-Ct tumor|) +/- SEM, and correlation coefficients among genes. Systematic comparison between candidates led us to the identification of a subset of suitable reference genes for clinical samples: IPO8, ACTB, POLR2A, 18S, and PPIA. Further analysis showed that IPO8 had a very low mean of |Delta Ct| (0.70 +/- 0.09), with no statistically significant differences between normal and malignant samples and with excellent expression stability.
Our data show that IPO8 is the most accurate reference gene for clinical lung specimens. In addition, we demonstrate that the commonly used genes GAPDH and HPRT1 are inappropriate to normalize data derived from lung biopsies, although they are suitable as reference genes for lung cell lines. We thus propose IPO8 as a novel reference gene for lung cancer samples.
肺癌中差异表达基因的准确标准化对于通过实时逆转录聚合酶链反应(RT-PCR)和微阵列鉴定新的治疗靶点和生物标志物至关重要。尽管经典的“管家”基因,如甘油醛-3-磷酸脱氢酶(GAPDH)、次黄嘌呤-鸟嘌呤磷酸核糖转移酶1(HPRT1)和β-肌动蛋白(beta-actin)过去已被广泛使用,但其作为肺组织参考基因的准确性尚未得到证实。
我们对一组用于肺标本和肺细胞系的16个候选参考基因进行了全面分析。通过定量实时RT-PCR测量基因表达,并使用GeNorm和NormFinder软件、|ΔCt|(=|Ct正常 - Ct肿瘤|)的平均值±标准误以及基因间的相关系数分析表达稳定性。候选基因之间的系统比较使我们确定了一组适用于临床样本的参考基因:IPO8、ACTB、POLR2A、18S和PPIA。进一步分析表明,IPO8的|ΔCt|平均值非常低(0.70±0.09),正常样本和恶性样本之间无统计学显著差异,且具有出色的表达稳定性。
我们的数据表明,IPO8是临床肺标本中最准确的参考基因。此外,我们证明常用基因GAPDH和HPRT1不适用于标准化来自肺活检的数据,尽管它们适合作为肺细胞系的参考基因。因此,我们提议将IPO8作为肺癌样本的新型参考基因。