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评价适用于研究甲状腺肿瘤中 mRNAs 和 microRNAs 表达的参考基因。

Evaluation of reference genes suitable for studying mRNAs and microRNAs expression in thyroid neoplasms.

机构信息

Pathology Department, Faculty of Medicine, Kuwait University, Kuwait.

出版信息

Pathol Res Pract. 2024 Oct;262:155519. doi: 10.1016/j.prp.2024.155519. Epub 2024 Aug 14.

Abstract

Analysis of gene expression is a pivotal method at the core of biomarkers studies and cancer research. Currently, RT-qPCR is the most commonly used technique to investigate the expression of certain genes. The accurate and reliable result relies on an effective normalization step using suitable reference genes. The present study was designed to evaluate the eligibility of a set of candidate mRNAs and snoRNA as reference genes in the most common human thyroid neoplasms. We tested the expression levels of eleven mRNA and small RNA housekeeping genes in thyroid samples. The stability of the candidate genes was examined in different thyroid lesions and under different experimental conditions. Results were compared to the reported data in the TCGA database. Our results suggested HPRT1 and ACTB as the best mRNA reference genes, SNORD96A, and SNORD95 as the best miRNA reference genes in thyroid tissues. These genes showed the most stable expression pattern among different thyroid lesions as well as different experimental conditions. The findings in this study highlight the effect of reference genes selection on data interpretation and emphasize the importance of testing for suitable reference genes to be used in specific types of cells and experimental conditions to ensure the validity and accuracy of results.

摘要

基因表达分析是生物标志物研究和癌症研究的核心方法。目前,实时荧光定量聚合酶链式反应(RT-qPCR)是研究特定基因表达最常用的技术。准确可靠的结果依赖于使用合适的参考基因进行有效的标准化步骤。本研究旨在评估一组候选 mRNA 和 snoRNA 作为最常见人类甲状腺肿瘤中参考基因的适用性。我们检测了 11 种 mRNA 和小核 RNA 管家基因在甲状腺样本中的表达水平。在不同的甲状腺病变和不同的实验条件下,候选基因的稳定性进行了检测。结果与 TCGA 数据库中报告的数据进行了比较。我们的结果表明,在甲状腺组织中,HPRT1 和 ACTB 是最佳的 mRNA 参考基因,SNORD96A 和 SNORD95 是最佳的 miRNA 参考基因。这些基因在不同的甲状腺病变以及不同的实验条件下表现出最稳定的表达模式。本研究的结果强调了参考基因选择对数据解释的影响,并强调了在特定类型的细胞和实验条件下测试合适的参考基因的重要性,以确保结果的有效性和准确性。

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