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Identification of reliable reference genes for quantitative gene expression studies in oral squamous cell carcinomas compared to adjacent normal tissues in the F344 rat model

机译:鉴定可靠的参考基因以进行F344大鼠模型中口腔鳞状细胞癌与相邻正常组织比较的定量基因表达研究

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Oral squamous cell carcinomas (OSCCs) induced in F344 rats by 4-nitroquinoline-l-oxide (4-NQO) demonstrate considerable phenotypic similarity to human oral cancers and the model has been widely used for carcinogenesis and chemoprevention studies. Molecular characterization of this model needs reliable reference genes (RGs) to avoid false positive and -negative results for proper interpretation of gene expression data between tumor and adjacent normal tissues. Microarray analysis of 11 pairs of OSCC and site-matched phenotypically normal oral tissues from 4-NQO-treated rats identified 10 stably expressed genes in OSCC compared to adjacent normal tissues (p>0.5, CV<15%) that could serve as potential RGs in this model. The commonly used 27 RGs in the rat were also analyzed based on microarray data and most of them were found unsuitable for RGs in this model. Traditional RGs such as ACTB and GAPDH were significantly altered in OSCC compared to adjacent normal tissues (p<0.01, n=11); however, the Hsp90ab1 was ranked as the best RG candidate and the combination of Hsp90ab1 and HPRT1 was identified by NormFinder to be a superior reference for gene normalization among the commonly used RGs. This result was also validated by RT-PCR based on the selected top RG candidate pool. These data suggest that there are no common RGs suitable for different models and RG(s) should be identified before gene expression analysis. We successfully identified Hsp90abl as a stable RG in 4-NQO-induced OSCC compared to adjacent normal tissues in F344 rats. The combination of two stably expressed genes may be a better option for gene normalization in tissue samples.
机译:4-硝基喹啉-1-氧化物(4-NQO)在F344大鼠中诱发的口腔鳞状细胞癌(OSCC)与人类口腔癌表现出可观的表型相似性,该模型已被广泛用于癌变和化学预防研究。该模型的分子表征需要可靠的参考基因(RGs)来避免错误的阳性和阴性结果,以便正确解释肿瘤与相邻正常组织之间的基因表达数据。对来自4-NQO处理的大鼠的11对OSCC和表型匹配的表型正常口腔组织的微阵列分析确定了OSCC中与相邻正常组织相比有10个稳定表达的基因(p> 0.5,CV <15%),可以作为潜在的RGs在这个模型中。还基于微阵列数据分析了大鼠中常用的27个RG,发现其中大多数不适用于该模型。与相邻的正常组织相比,传统的RGs(如ACTB和GAPDH)在OSCC中发生了显着改变(p <0.01,n = 11)。然而,Hsp90ab1被列为最佳RG候选者,并且NormFinder将Hsp90ab1和HPRT1的组合鉴定为常用RG中基因标准化的最佳参考。该结果还通过基于选定的顶级RG候选库的RT-PCR进行了验证。这些数据表明,没有适用于不同模型的常见RG,并且在基因表达分析之前应先鉴定RG。我们成功地鉴定了Hsp90abl是与F344大鼠相邻的正常组织相比在4-NQO诱导的OSCC中稳定的RG。两个稳定表达的基因的组合可能是组织样本中基因正常化的更好选择。

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