首页> 外文期刊>Molecular and Cellular Probes: The Location, Diagnosis and Monitoring of Disease by Specific Molecules and Cell Lines >Housekeeping gene variability in normal and cancerous colorectal, pancreatic, esophageal, gastric and hepatic tissues.
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Housekeeping gene variability in normal and cancerous colorectal, pancreatic, esophageal, gastric and hepatic tissues.

机译:在正常和癌性大肠,胰腺,食道,胃和肝组织中的管家基因变异性。

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摘要

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.
机译:仔细的归一化对于活组织大小的组织样品中的mRNA水平的准确定量至关重要。通常,应用以内源性标准(主要是管家基因(HKG))标准化目标基因。然而,已经报道了不同组织和病理状态之间内源参考基因表达水平的差异。因此,我们面临的挑战是鉴定一组内源参考基因,其正常和癌变组织之间的mRNA表达水平不会明显改变。与相应的正常组织相比,采用实时定量PCR(Q-RT-PCR)分析来评估大肠癌,胰腺癌,食管癌和胃癌中21种经典管家基因以及肝转移中21种经典管家基因的基因表达差异。我们的结果表明,一些管家基因是在一些被调查组织中具有相对稳定基因表达的候选基因,但是对于大多数接受调查的HKG,我们的数据显示出不同组织和病理状态之间基因表达变异程度的明显差异。但是,对于所研究的五个组织中的每一个,我们发现了一组以恒定水平表达的基因,因此代表了一组候选基因,我们可以推荐它们作为各自组织类型中的持家基因。总而言之,我们的研究结果可为其他科学家研究各种癌,以组织特异性选择最佳管家基因(HKG)来指导目标基因表达正常化提供指导。

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