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尿液细胞外囊泡生物标志物的障碍:迈向临床应用

Roadblocks of Urinary EV Biomarkers: Moving Toward the Clinic.

作者信息

Droste Marvin, Puhka Maija, van Royen Martin E, Ng Monica S Y, Blijdorp Charles, Alvarez-Llamas Gloria, Borràs Francesc E, Büscher Anja K, Bussolati Benedetta, Dear James W, Falcón-Pérez Juan M, Giebel Bernd, Grange Cristina, Hoorn Ewout J, Leivo Janne, Lenassi Metka, Llorente Alicia, Lucien Fabrice, Mertens Inge, Mischak Harald, Pink Desmond, Tertel Tobias, Tiwari Swasti, Vizio Dolores Di, Yuen Peter S T, Zarovni Natasa, Jenster Guido, Burger Dylan, Martens-Uzunova Elena S, Erdbrügger Uta

机构信息

Department II of Internal Medicine, University of Cologne, Faculty of Medicine and University Hospital Cologne, Cologne, Germany.

Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.

出版信息

J Extracell Vesicles. 2025 Jul;14(7):e70120. doi: 10.1002/jev2.70120.

Abstract

Despite remarkable interest in the biomarker potential of urinary extracellular vesicles (uEVs) and the identification of numerous promising candidates, their clinical translation still presents multiple challenges. The opportunities for successful translation are obvious, yet the main roadblocks on the way have hardly been systematically considered and more coordinated approaches are needed to overcome them. In the present review article, we have identified the most relevant roadblocks of clinical translation of urinary EV-based biomarkers and discuss possible solutions to overcome them. These roadblocks are categorized as fundamental and technical but also related to development of novel biomarker assays and clinical acceptance. In addition, hurdles within the regulatory approval process are discussed. It is clear that various roadblocks to clinical translation of urinary EV biomarkers exist; however, they are addressable by promoting rigor and reproducibility as well as collaboration between basic and clinical scientists, clinicians, industry and regulatory bodies. Moreover, knowledge of obstacles for assay development and regulatory requirements should already be considered when developing a new biomarker to maximize the chance of successful translation. This review presents not only a status quo, but also a roadmap for the further development of the field.

摘要

尽管人们对尿液细胞外囊泡(uEVs)的生物标志物潜力有着浓厚兴趣,并鉴定出了众多有前景的候选物,但其临床转化仍面临多重挑战。成功转化的机会显而易见,但前进道路上的主要障碍却几乎未得到系统考量,因此需要更协调一致的方法来克服这些障碍。在本综述文章中,我们确定了基于尿液细胞外囊泡的生物标志物临床转化中最相关的障碍,并讨论了克服这些障碍的可能解决方案。这些障碍分为基础和技术方面,也与新型生物标志物检测方法的开发及临床接受度有关。此外,还讨论了监管审批过程中的障碍。显然,尿液细胞外囊泡生物标志物的临床转化存在各种障碍;然而,通过提高严谨性和可重复性,以及基础科学家与临床科学家、临床医生、行业和监管机构之间的合作,可以解决这些障碍。此外,在开发新生物标志物时,就应考虑检测方法开发的障碍和监管要求方面的知识,以最大限度地提高成功转化的机会。本综述不仅呈现了该领域的现状,还为其进一步发展提供了路线图。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf69/12269535/e7f1d8c4304a/JEV2-14-e70120-g006.jpg

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