Tetraspanin immunoassay for the detection of extracellular vesicles and renal cell carcinoma

Author:

Khan Misba12ORCID,Islam Md. Khirul12,Rahman Mafiur1,Dhondt Bert34,Quintero Ileana56,Puhka Maija56,Jaakkola Panu M.27,Lamminmäki Urpo12,Leivo Janne12

Affiliation:

1. Department of Life Technologies Division of Biotechnology University of Turku Turku Finland

2. InFLAMES Research Flagship Center University of Turku Turku Finland

3. Department of Urology Ghent University Hospital Ghent Belgium

4. Cancer Research Institute Ghent University Ghent Belgium

5. EV and HiPrep Core Institute for Molecular Medicine Finland FIMM University of Helsinki Helsinki Finland

6. EV‐core facility University of Helsinki Helsinki Finland

7. Department of Oncology and Radiotherapy and FICAN West Cancer Centre University of Turku and Turku University Hospital Turku Finland

Abstract

AbstractHalf of patients with renal cell carcinoma (RCC) develop metastases. New and noninvasive biomarkers are needed for the diagnosis of RCC. The study aims to develop an EV‐based assay for the detection of RCC using a highly sensitive nanoparticle‐aided time‐resolved fluorescence immunoassay (NP‐TRFIA). To confirm the presence of tetraspanins on EVs, size exclusion chromatography is used to separate EV‐ and PE‐fractions from RCC4, 786‐O, and HEK293 cell lines. EV‐ and PE‐fractions are quantified using NP‐TRFIA assays established for CD9, CD63, CD81, and CD151. Tetraspanins are measured from RCC CCM and serum samples of RCC (n = 14), benign (n = 17), and healthy (n = 9) individuals. Among the tetraspanins, CD63 exhibits 3‐5‐fold higher expression on RCC4 and 786‐O CCM compared to HEK293. A sandwich CD63‐CD63 assay demonstrates significant discrimination of RCC patients from benign (p = 0.0003), and healthy (p = 0.005) individuals, respectively. Similarly, the CD81‐CD81 assay also enables significant separation of RCC patients compared to benign (p = 0.014), and healthy (p = 0.003) controls, respectively. This suggests that RCC cell lines and serum of RCC patients show higher amounts of CD63‐ and CD81‐EVs compared to controls. Detection of these EVs using NP‐TRFIA approach may play a vital role in the detection of RCC.

Publisher

Wiley

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