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首页> 外文期刊>Veterinary Pathology >MicroRNA Expression in Formalin-Fixed, Paraffin-Embedded Samples of Canine Cutaneous and Oral Melanoma by RT-qPCR
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MicroRNA Expression in Formalin-Fixed, Paraffin-Embedded Samples of Canine Cutaneous and Oral Melanoma by RT-qPCR

机译:通过RT-QPCR在福尔马林固定的,石蜡包裹的石蜡嵌入样品的MicroRNA表达

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MicroRNAs (miRNAs) are a class of small, noncoding RNA that post-transcriptionally regulate protein expression. miRNAs are emerging as clinical biomarkers of many diseases, including tumors. The aim of this study was to investigate whether miRNA expression could vary in melanoma samples derived from formalin-fixed, paraffin-embedded (FFPE) tissues. The study included 4 groups: (1) 9 samples of oral canine malignant melanoma, (2) 10 samples of cutaneous malignant melanoma, (3) 5 samples of healthy oral mucosa, and (4) 7 samples of healthy skin. The expression levels of 6 miRNAs-miR-145, miR-146a, miR-425-5p, miR-223, miR-365, and miR-134-were detected and assessed by quantitative reverse transcription polymerase chain reaction (RT-qPCR) using TaqMan probes. Cutaneous canine malignant melanoma showed a decrease of the expression level of miR-145 and miR-365 and an increase of miR-146a and miR-425-5p compared to control samples. MiR-145 was also downregulated in oral canine malignant melanoma. The miRNAs with decreased expression may regulate genes involved in RAS, Rap1, and transforming growth factor beta (TGF-beta) signaling pathways, as well as upregulated genes associated with phosphatidylinositol signaling system, adherens junction, and RAS signaling pathways. In conclusion, miR-145, miR-365, miR-146a, and miR-425-5p were differentially expressed in canine malignant melanoma and healthy FFPE samples, suggesting that they may play a role in canine malignant melanoma pathogenesis.
机译:MicroRNAS(miRNA)是一类小型非编码RNA,其后转录蛋白表达。 MiRNA正在成为许多疾病的临床生物标志物,包括肿瘤。本研究的目的是研究MiRNA表达是否可以在源自福尔马林固定的石蜡包埋(FFPE)组织中的黑色素瘤样品中变化。该研究包括4组:(1)9口服犬恶性黑素瘤样品,(2)10个皮肤恶性黑素瘤样品,(3)5个健康口腔粘膜样品,(4)7个健康皮肤样品。通过定量逆转录聚合酶链反应(RT-QPCR)检测和评估6 miRNA-miR-145,miR-146a,miR-425-5p,miR-223,miR-365和miR-134的表达水平。使用Taqman探针。皮肤犬恶性黑色素瘤显示MIR-145和miR-365的表达水平降低以及与对照样品相比的miR-146a和miR-425-5p的增加。 MiR-145也在口服犬恶性黑色素瘤中下调。具有降低的表达可能调节参与RA,RAP1和转化生长因子β(TGF-BETA)信号传导途径的基因,以及与磷脂酰肌醇信号传导系统,粘附结和RA信号通路相关的上调基因。总之,MiR-145,miR-365,miR-146a和miR-425-5p在犬恶性黑素瘤和健康的FFPE样品中差异表达,表明它们可能在犬恶性黑色素瘤发病机制中发挥作用。

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