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首页> 外文期刊>International Journal of Cancer =: Journal International du Cancer >MicroRNA expression profiling in bladder cancer: the challenge of next-generation sequencing in tissues and biofluids
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MicroRNA expression profiling in bladder cancer: the challenge of next-generation sequencing in tissues and biofluids

机译:microRNA表达剖析在膀胱癌中:组织和生物流体中下一代测序的挑战

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摘要

Bladder cancer (BC) is a heterogeneous disease characterized by a high recurrence rate that necessitates continuous cystoscopic surveillance. MicroRNAs (miRNAs) are detectable in tissues and biofluids such as plasma/serum and urine. They represent promising biomarkers with potential not only for detecting BC but also informing on prognosis and monitoring treatment response. In this review, the many aspects of the application of next-generation sequencing (NGS) to evaluate miRNA expression in BC is discussed, including technical issues as well as a comparison with results obtained by qRT-PCR. The available studies investigating miRNA profiling in BC by NGS are described, with particular attention to the potential applicability on biofluids. Altered miRNA levels have been observed in BC tissues by NGS, but these results so far only partially overlapped among studies and with previous data obtained by qRT-PCR. The discrepancies can be ascribed to the small groups of BC patients sequenced. The few available studies on biofluids are mainly focused on implementing RNA isolation and sequencing workflow. Using NGS to analyze miRNAs in biofluids can potentially provide results comparable to tissues with no invasive procedures for the patients. In particular, the analyses performed on exosomes/microvesicles appear to be more informative. Thanks to the improvement of both wet-lab procedures and pipelines/tools for data analyses, NGS studies on biofluids will be performed on a larger scale. MiRNAs detected in urine and serum/plasma will demonstrate their potentiality to describe the variegated scenario of BC and to become relevant clinical markers.
机译:膀胱癌(BC)是一种异质性疾病,其特征在于一种高复发率,需要连续膀胱镜监测。 MicroRNAs(miRNA)可在组织和生物流体中可检测,例如血浆/血清和尿液。它们代表有前途的生物标志物,不仅具有检测BC的潜力,而且还通知预后和监测治疗反应。在该评论中,讨论了在BC中施加下一代测序(NGS)来评估BC中的miRNA表达的许多方面,包括技术问题以及通过QRT-PCR获得的结果进行比较。描述了NGS在BCS中调查miRNA分析的可用研究,特别注意了对生物流体的潜在适用性。通过NGS在BC组织中观察到改变的miRNA水平,但到目前为止,这些结果仅部分地重叠研究,并且通过QRT-PCR获得的先前数据。差异可以归因于测序的小组患者。对生物流体的一些可用研究主要集中在实施RNA隔离和测序工作流程。使用NGS在生物流体中分析miRNA可以提供与患者没有侵入手术的组织相当的结果。特别地,对外泌体/微泡的分析似乎更有信息。由于改善了湿效果程序和管道/数据分析的工具,NGS对生物流体的研究将以更大的规模进行。在尿液和血清/等离子体中检测到的miRNA将展示他们描述BC的杂种场景并成为相关的临床标志物的潜力。

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