School of Medical Sciences, University of Campinas, Campinas 13083894, Brazil.
Faculty of Pharmaceutical Sciences, University of Campinas, Campinas 13083970, Brazil.
Int J Mol Sci. 2023 Jun 29;24(13):10884. doi: 10.3390/ijms241310884.
The microRNA (miRNA) expression profile by qRT-PCR depends directly on the most appropriate normalization strategy adopted; however, currently there is no universally adequate reference gene. Therefore, this study aimed to determine, considering RNA-Seq results, the most adequate endogenous normalizer for use in the relative quantification of urine miRNAs from head and neck cancer patients, treated with cisplatin chemoradiotherapy. The massive sequencing was performed to identify the miRNAs differentially expressed between the group with cisplatin nephrotoxicity ( = 6) and the one without ( = 6). The candidate endogen normalizer was chosen according to four criteria: (1) the miRNA must be expressed in most samples; (2) the miRNA must have a fold change value between 0.99 and 1.01; (3) the miRNA must have a -value ≥ 0.98; and (4) the miRNA must not be commented on by the final GeneGlobe (Qiagen, Hilden, Germany) analysis. Four miRNAs met all the criteria (hsa-miR-363-5p, hsa-miR-875-5p, hsa-miR-4302, and hsa-miR-6749-5p) and were selected for validation by qRT-PCR in a cohort of 49 patients (including the 12 sequencing participants). Only hsa-miR-875-5p was shown to be an adequate normalizer for the experimental condition under investigation, as it exhibited invariant expression between the two groups.
实时定量 PCR (qRT-PCR) 的 microRNA (miRNA) 表达谱直接取决于所采用的最合适的归一化策略; 然而,目前还没有普遍适用的参考基因。因此,本研究旨在根据 RNA-Seq 结果,确定最适合用于头颈部癌症患者顺铂放化疗后尿液 miRNA 相对定量的内源性正常化基因。进行大规模测序以鉴定具有顺铂肾毒性组(n = 6)和无顺铂肾毒性组(n = 6)之间差异表达的 miRNA。候选内源性正常化基因是根据四个标准选择的:(1) miRNA 必须在大多数样本中表达;(2) miRNA 的 fold change 值必须在 0.99 和 1.01 之间;(3) miRNA 的 -value ≥ 0.98;(4) miRNA 不得由最终的 GeneGlobe (Qiagen, Hilden, Germany) 分析进行注释。有 4 个 miRNA 符合所有标准(hsa-miR-363-5p、hsa-miR-875-5p、hsa-miR-4302 和 hsa-miR-6749-5p),并在 49 例患者(包括 12 例测序参与者)队列中通过 qRT-PCR 进行验证。只有 hsa-miR-875-5p 被证明是实验条件下的合适归一化基因,因为它在两组之间的表达不变。