Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.
Department of Equine and Small Animal Medicine, Faculty of Veterinary Medicine, University of Helsinki, Helsinki, Finland.
Sci Rep. 2024 Aug 2;14(1):17967. doi: 10.1038/s41598-024-69070-7.
Current diagnostic methods for canine urothelial carcinoma (UC) are technically challenging or can lack specificity, hence there is a need for novel biomarkers of UC. To this end, we analysed the microRNA (miRNA) cargo of extracellular vesicles (EVs) from urine samples of dogs with UC to identify candidate miRNA biomarkers. Urine was fractionated using ultrafiltration combined with size-exclusion chromatography and small RNA sequencing analysis was performed on both the EV enriched and (EV free) protein fractions. A greater number of candidate miRNA biomarkers were detected in the EV fraction than the protein fraction, and further validation using droplet digital PCR (ddPCR) was performed on the EV enriched fraction of a second cohort of dogs with UC which indicated that miR-182, miR-221 and miR-222 were significantly overrepresented in dogs with UC when compared with healthy dogs and dogs with urinary tract infections. Pathway analysis confirmed that these three miRNAs are involved in cancer. In addition, their potential downstream gene targets were predicted and PIK3R1, a well-known oncogene is likely to be a shared target between miRNA-182 and miRNA-221/222. In summary, this study highlights the potential of urinary EV-associated miRNAs as a source of biomarkers for the diagnosis of canine UC.
目前用于犬尿路上皮癌 (UC) 的诊断方法技术上具有挑战性或特异性不足,因此需要 UC 的新型生物标志物。为此,我们分析了来自 UC 犬尿液样本中外泌体 (EV) 的 microRNA (miRNA) 货物,以鉴定候选 miRNA 生物标志物。使用超滤结合大小排阻色谱法对尿液进行分级,对 EV 富集和 (EV 无) 蛋白级分进行小 RNA 测序分析。在 EV 级分中检测到的候选 miRNA 生物标志物数量多于蛋白级分,并且在第二个 UC 犬队列的 EV 富集级分中使用液滴数字 PCR (ddPCR) 进行了进一步验证,结果表明与健康犬和患有尿路感染的犬相比,UC 犬中 miR-182、miR-221 和 miR-222 明显过表达。通路分析证实这三个 miRNAs 参与癌症。此外,还预测了它们潜在的下游基因靶标,并且 PIK3R1(一种众所周知的癌基因)可能是 miRNA-182 和 miRNA-221/222 的共同靶标。总之,这项研究强调了尿 EV 相关 miRNA 作为犬 UC 诊断生物标志物的潜在来源。