Strømme Olaf, Heck Kathleen A, Brede Gaute, Lindholm Håvard T, Otterlei Marit, Arum Carl-Jørgen
Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, 7491 Trondheim, Norway.
CEMIR-Centre of Molecular Inflammation Research, Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, 7491 Trondheim, Norway.
Curr Issues Mol Biol. 2021 Jun 4;43(1):286-300. doi: 10.3390/cimb43010024.
Bladder cancer (BC) is currently diagnosed and monitored by cystoscopy, a costly and invasive procedure. Potential biomarkers in urine, blood, and, more recently, extracellular vesicles (EVs), have been explored as non-invasive alternatives for diagnosis and surveillance of BC. EVs are nanovesicles secreted by most cell types containing diverse molecular cargo, including different types of small RNAs, such as microRNA (miRNA). In this study, we performed next-generation sequencing of EV-contained miRNA isolated from urine and serum of 41 patients with non-muscle invasive BC (27 stage Ta, 14 stage T1) and 15 non-cancer patients (NCP) with benign cystoscopy findings. MiRNA sequencing was also performed on serum supernatant samples for T1 patients. To identify potential BC-specific biomarkers, expression levels of miRNA in presurgery samples were compared to those at postsurgery check-ups, and to NCPs. Results showed that two miRNAs, urinary EV-contained miR-451a and miR-486-5p, were significantly upregulated in presurgery samples from T1 patients compared to postsurgery check-up samples. This was confirmed in a replica EV/RNA isolation and sequencing run of 10 T1 patients from the primary run; however, analyses revealed no differential expression of miRNAs in serum EVs, serum supernatant, or when comparing BC patients to NCPs. This is the first study to investigate EV-containing miRNA sequencing in pre- and postsurgery BC patient samples and our findings suggest that urinary EV-contained miR-451a and miR-486-5p may be potential biomarkers for recurrence-free survival of BC patients with stage T1 disease.
膀胱癌(BC)目前通过膀胱镜检查进行诊断和监测,这是一种成本高昂且具有侵入性的检查方法。尿液、血液以及最近发现的细胞外囊泡(EVs)中的潜在生物标志物已被探索作为膀胱癌诊断和监测的非侵入性替代方法。EVs是大多数细胞类型分泌的纳米囊泡,包含多种分子成分,包括不同类型的小RNA,如微小RNA(miRNA)。在本研究中,我们对41例非肌层浸润性膀胱癌患者(27例Ta期,14例T1期)和15例膀胱镜检查结果为良性的非癌症患者(NCP)的尿液和血清中分离出的含EVs的miRNA进行了二代测序。对T1期患者的血清上清样本也进行了miRNA测序。为了确定潜在的膀胱癌特异性生物标志物,将术前样本中的miRNA表达水平与术后复查样本以及NCPs的表达水平进行了比较。结果显示,与术后复查样本相比,T1期患者术前样本中尿液含EVs的miR-451a和miR-486-5p这两种miRNA显著上调。在对初次检测的10例T1期患者进行的重复EV/RNA分离和测序中得到了证实;然而,分析显示血清EVs、血清上清中miRNA没有差异表达,将膀胱癌患者与NCPs进行比较时也未发现差异表达。这是第一项研究膀胱癌患者手术前后样本中含EVs的miRNA测序的研究,我们的研究结果表明,尿液含EVs的miR-451a和miR-486-5p可能是T1期膀胱癌患者无复发生存的潜在生物标志物。