Influence of RT-qPCR primer position on EGFR interference efficacy in lung cancer cells

被引：31

作者：

Chen, Gang ^{[1
,2
,3
]}

Kronenberger, Peter ^{[1
,2
,4
]}

Teugels, Erik ^{[1
,2
]}

De Greve, Jacques ^{[1
,2
]}

机构：

[1] Vrije Univ Brussel, Univ Ziekenhuis Brussel, Mol Oncol Lab, Brussels, Belgium

[2] Vrije Univ Brussel, Univ Ziekenhuis Brussel, Dept Med Oncol, Brussels, Belgium

[3] Guangxi Med Univ, Affiliated Hosp 1, Dept Pathol, Nanning, Guangxi, Peoples R China

[4] Erasmushgsk Brussel, Dept Gezondheidszorg, Biotechnol Lab, Brussels, Belgium

来源：

BIOLOGICAL PROCEDURES ONLINE | 2011年 / 13卷

关键词：

QUANTITATIVE PCR; RNA INTERFERENCE;

D O I：

10.1186/1480-9222-13-1

中图分类号：

Q5 [生物化学];

学科分类号：

071010 ; 081704 ;

摘要：

Background: Real-time quantitative RT-PCR (RT-qPCR) is a "gold" standard for measuring steady state mRNA levels in RNA interference assays. The knockdown of the epidermal growth factor receptor (EGFR) gene with eight individual EGFR small interfering RNAs (siRNAs) was estimated by RT-qPCR using three different RT-qPCR primer sets. Results: Our results indicate that accurate measurement of siRNA efficacy by RT-qPCR requires careful attention for the selection of the primers used to amplify the target EGFR mRNA. Conclusions: We conclude that when assessing siRNA efficacy with RT-qPCR, more than one primer set targeting different regions of the mRNA should be evaluated and at least one of these primer sets should amplify a region encompassing the siRNA recognition sequence.

引用

页数：7

共 7 条

[1] Allelic dilution obscures detection of a biologically significant resistance mutation in EGFR-amplified lung cancer [J].