Extracellular vesicle-associated miRNAs in ovarian cancer – design of an integrated NGS-based workflow for the identification of blood-based biomarkers for platinum-resistance

Author:

Kuhlmann Jan Dominik123,Chebouti Issam34,Kimmig Rainer34,Buderath Paul34,Reuter Michael5,Puppel Sven-Holger5,Wimberger Pauline123,Kasimir-Bauer Sabine34

Affiliation:

1. Department of Gynecology and Obstetrics , Medical Faculty and University Hospital Carl Gustav Carus, Technische Universität Dresden , Dresden , Germany

2. National Center for Tumor Diseases (NCT), Partner Site Dresden , Dresden , Germany

3. German Cancer Consortium (DKTK), Dresden and German Cancer Research Center (DKFZ) , Heidelberg , Germany

4. Department of Gynecology and Obstetrics , University Hospital Essen , Essen , Germany

5. Department of Diagnostics , Fraunhofer Institute for Cell Therapy and Immunology , Leipzig , Germany

Abstract

Abstract Background Extracellular vesicle (EV)-associated microRNAs (miRNAs) have been suggested as promising biomarkers for blood-based cancer diagnosis. However, one of the major limitations for the use of EVs with diagnostic purpose is the lack of standardized EV-profiling techniques. In this regard, the objective of our study was to design an integrated next-generation sequencing (NGS)-based workflow for analyzing the signature of EV-associated miRNA in the plasma of platinum-resistant ovarian cancer patients. Methods For EV-extraction, different enrichment methods were compared (ExoQuick vs. exoRNeasy). NGS was performed with the Illumina platform. Results We established an integrated NGS-based workflow, including EV-enrichment with the ExoQuick system, which resulted in an optimal RNA-yield and consistent small RNA libraries. We applied this workflow in a pilot cohort of clinically documented platinum-sensitive (n=15) vs. platinum-resistant (n=15) ovarian cancer patients, resulting in a panel of mature EV-associated miRNAs (including ovarian cancer associated miR-181a, miR-1908, miR-21, miR-486 and miR-223), which were differentially abundant in the plasma of platinum-resistant patients. Conclusions This is the first study, analyzing the profile of EV-associated miRNAs in platinum-resistant ovarian cancer patients. We provide rationale to further validate these miRNA candidates in an independent set of patients, in order to characterize their biomarker potential as predictors for platinum-resistance.

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

Reference43 articles.

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