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使用定量逆转录聚合酶链反应(qRT-PCR)选择用于胶质母细胞瘤表达分析的合适管家基因。

Selection of suitable housekeeping genes for expression analysis in glioblastoma using quantitative RT-PCR.

作者信息

Valente Valeria, Teixeira Silvia A, Neder Luciano, Okamoto Oswaldo K, Oba-Shinjo Sueli M, Marie Suely K N, Scrideli Carlos A, Paçó-Larson Maria L, Carlotti Carlos G

机构信息

Department of Surgery and Anatomy, Faculty of Medicine, University of São Paulo, Av, dos Bandeirantes 3900, 140490-900, Ribeirão Preto, SP, Brazil.

出版信息

BMC Mol Biol. 2009 Mar 3;10:17. doi: 10.1186/1471-2199-10-17.

DOI:10.1186/1471-2199-10-17
PMID:19257903
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2661085/
Abstract

BACKGROUND

Considering the broad variation in the expression of housekeeping genes among tissues and experimental situations, studies using quantitative RT-PCR require strict definition of adequate endogenous controls. For glioblastoma, the most common type of tumor in the central nervous system, there was no previous report regarding this issue.

RESULTS

Here we show that amongst seven frequently used housekeeping genes TBP and HPRT1 are adequate references for glioblastoma gene expression analysis. Evaluation of the expression levels of 12 target genes utilizing different endogenous controls revealed that the normalization method applied might introduce errors in the estimation of relative quantities. Genes presenting expression levels which do not significantly differ between tumor and normal tissues can be considered either increased or decreased if unsuitable reference genes are applied. Most importantly, genes showing significant differences in expression levels between tumor and normal tissues can be missed. We also demonstrated that the Holliday Junction Recognizing Protein, a novel DNA repair protein over expressed in lung cancer, is extremely over-expressed in glioblastoma, with a median change of about 134 fold.

CONCLUSION

Altogether, our data show the relevance of previous validation of candidate control genes for each experimental model and indicate TBP plus HPRT1 as suitable references for studies on glioblastoma gene expression.

摘要

背景

鉴于管家基因在不同组织和实验条件下的表达存在广泛差异,使用定量逆转录聚合酶链反应(qRT-PCR)的研究需要严格定义合适的内参基因。对于中枢神经系统最常见的肿瘤类型胶质母细胞瘤,此前尚无关于此问题的报道。

结果

我们在此表明,在七个常用的管家基因中,TBP和HPRT1是胶质母细胞瘤基因表达分析的合适参照基因。利用不同内参基因评估12个靶基因的表达水平显示,所应用的标准化方法可能会在相对量的估计中引入误差。如果使用不合适的参照基因,肿瘤组织和正常组织中表达水平无显著差异的基因可能会被认为表达量增加或减少。最重要的是,肿瘤组织和正常组织中表达水平存在显著差异的基因可能会被遗漏。我们还证明,一种在肺癌中过表达的新型DNA修复蛋白——霍利迪连接识别蛋白(Holliday Junction Recognizing Protein),在胶质母细胞瘤中极度过表达,中位数变化约为134倍。

结论

总之,我们的数据表明了对每个实验模型的候选对照基因进行预先验证的相关性,并指出TBP加HPRT1是胶质母细胞瘤基因表达研究的合适参照基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b92f/2661085/dda35151d12b/1471-2199-10-17-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b92f/2661085/2550a7858d7c/1471-2199-10-17-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b92f/2661085/60205a7df762/1471-2199-10-17-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b92f/2661085/32e0dd7fc61f/1471-2199-10-17-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b92f/2661085/dda35151d12b/1471-2199-10-17-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b92f/2661085/2550a7858d7c/1471-2199-10-17-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b92f/2661085/60205a7df762/1471-2199-10-17-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b92f/2661085/32e0dd7fc61f/1471-2199-10-17-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b92f/2661085/dda35151d12b/1471-2199-10-17-4.jpg

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