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Identification of Optimal Reference Genes for Gene Expression Normalization in a Wide Cohort of Endometrioid Endometrial Carcinoma Tissues

机译:广泛的子宫内膜样子宫内膜癌组织中基因表达正常化的最佳参考基因的鉴定

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摘要

Accurate normalization is a primary component of a reliable gene expression analysis based on qRT-PCR technique. While the use of one or more reference genes as internal controls is commonly accepted as the most appropriate normalization strategy, many qPCR-based published studies still contain data poorly normalized and reference genes arbitrarily chosen irrespective of the particular tissue and the specific experimental design. To date, no validated reference genes have been identified for endometrial cancer tissues. In this study, 10 normalization genes (GAPDH, B2M, ACTB, POLR2A, UBC, PPIA, HPRT1, GUSB, TBP, H3F3A) belonging to different functional and abundance classes in various tissues and used in different studies, were analyzed to determine their applicability. In total, 100 endometrioid endometrial cancer samples, which were carefully balanced according to their tumor grade, and 29 normal endometrial tissues were examined using SYBR Green Real-Time RT-PCR. The expression stability of candidate reference genes was determined and compared by means of geNorm and NormFinder softwares. Both algorithms were in agreement in identifying GAPDH, H3F3A, PPIA, and HPRT1 as the most stably expressed genes, only differing in their ranking order. Analysis performed on the expression levels of all candidate genes confirm HPRT1 and PPIA as the most stably expressed in the study groups regardless of sample type, to be used alone or better in combination. As the stable expression of HPRT1 and PPIA between normal and tumor endometrial samples fulfill the basic requirement of a reference gene to be used for normalization purposes, HPRT1 expression showed significant differences between samples from low-grade and high-grade tumors. In conclusion, our results recommend the use of PPIA as a single reference gene to be considered for improved reliability of normalization in gene expression studies involving endometrial tumor samples at different tumor degrees.
机译:准确的标准化是基于qRT-PCR技术的可靠基因表达分析的主要组成部分。尽管普遍认为使用一种或多种参考基因作为内部对照是最合适的标准化策略,但许多基于qPCR的已发表研究仍包含标准化程度较差的数据和任意选择的参考基因,无论具体组织和具体实验设计如何。迄今为止,还没有为子宫内膜癌组织鉴定出有效的参考基因。在这项研究中,分析了10种归一化基因(GAPDH,B2M,ACTB,POLR2A,UBC,PPIA,HPRT1,GUSB,TBP,H3F3A),它们在不同的组织中属于不同的功能和丰度类别,并在不同的研究中使用,以确定其适用性。 。使用SYBR Green Real-Time RT-PCR,共检查了100个子宫内膜样子宫内膜癌样品,并根据其肿瘤等级对其进行了仔细平衡,并对29个正常子宫内膜组织进行了检查。确定候选参考基因的表达稳定性,并通过geNorm和NormFinder软件进行比较。两种算法在确定GAPDH,H3F3A,PPIA和HPRT1是最稳定表达的基因方面都一致,只是它们的排列顺序不同。对所有候选基因表达水平的分析证实,无论样品类型如何,HPRT1和PPIA在研究组中表达最稳定,可以单独使用或更好地组合使用。由于正常和肿瘤子宫内膜样品之间HPRT1和PPIA的稳定表达满足用于标准化目的的参考基因的基本要求,因此HPRT1表达在低度和高度肿瘤样品之间显示出显着差异。总之,我们的结果推荐使用PPIA作为单个参考基因,以提高涉及不同肿瘤程度的子宫内膜肿瘤样品的基因表达研究中归一化的可靠性。

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