Rubie Claudia, Kempf Katja, Hans Joachim, Su Tiefen, Tilton Bettina, Georg Thomas, Brittner Brigitte, Ludwig Bianca, Schilling Martin
Department of General, Vascular and Paediatric Surgery, University of the Saarland, Chirurgische Klinik, Gebäude 57, Homburg/Saar 66421, Germany.
Mol Cell Probes. 2005 Apr;19(2):101-9. doi: 10.1016/j.mcp.2004.10.001. Epub 2004 Dec 15.
Careful normalization is essential for the accurate quantitation of mRNA levels in biopsy-sized tissue samples. Commonly, normalization of the target gene with an endogenous standard, mainly housekeeping genes (HKGs), is applied. However, differences in the expression levels of endogenous reference genes have been reported between different tissues and pathological states. Therefore, we were challenged to identify a set of endogenous reference genes whose mRNA expression levels would not change significantly between normal and cancerous tissues. Quantitative real-time PCR (Q-RT-PCR) analysis was applied to evaluate the variability in gene expression among 21 classical housekeeping genes in colorectal, pancreatic, esophageal and gastric cancer as well as in liver metastases in comparison to the corresponding normal tissue. Our results indicated that some housekeeping genes were candidates with relatively stable gene expression in several of the investigated tissues but for most of the HKGs under investigation our data have revealed distinct differences in the extent of variability in gene expression between the different tissues and pathological states. However, for each of the five tissues investigated we found a group of genes that were expressed at a constant level thus representing a panel of candidates that we can recommend as housekeeping genes in the respective tissue types. In summary, our results can be used as guidance for other scientists studying various carcinomas for tissue-specific selection of the optimal housekeeping gene (HKG) to be used in normalizing target gene expression.
对于活检大小的组织样本中mRNA水平的准确定量而言,仔细的标准化至关重要。通常,会将目标基因与内源性标准(主要是管家基因)进行标准化。然而,已有报道称不同组织和病理状态之间内源性参考基因的表达水平存在差异。因此,我们面临着识别一组内源性参考基因的挑战,这些基因的mRNA表达水平在正常组织和癌组织之间不会有显著变化。应用定量实时PCR(Q-RT-PCR)分析来评估21个经典管家基因在结直肠癌、胰腺癌、食管癌和胃癌以及肝转移灶与相应正常组织中基因表达的变异性。我们的结果表明,一些管家基因在部分被研究组织中是基因表达相对稳定的候选基因,但对于大多数被研究的管家基因,我们的数据显示不同组织和病理状态之间基因表达变异性的程度存在明显差异。然而,对于所研究的五种组织中的每一种,我们都发现了一组以恒定水平表达的基因,因此代表了一组我们可以推荐作为各自组织类型中管家基因的候选基因。总之,我们的结果可为其他研究各种癌症的科学家在进行组织特异性选择最佳管家基因以标准化目标基因表达时提供指导。