Your browser doesn't support javascript.
loading
Integrins are enriched on aberrantly fucosylated tumour-derived urinary extracellular vesicles.
Islam, Md Khirul; Dhondt, Bert; Syed, Parvez; Khan, Misba; Gidwani, Kamlesh; Webber, Jason; Hendrix, An; Jenster, Guido; Lamminen, Tarja; Boström, Peter J; Pettersson, Kim; Lamminmäki, Urpo; Leivo, Janne.
Afiliação
  • Islam MK; Department of Life Technologies Division of Biotechnology University of Turku Turku Finland.
  • Dhondt B; InFLAMES Research Flagship Center University of Turku Turku Finland.
  • Syed P; Department of Urology Ghent University Hospital Ghent Belgium.
  • Khan M; Laboratory for Experimental Cancer Research Department of Human Structure and Repair Ghent University Ghent Belgium.
  • Gidwani K; Cancer Research Institute Ghent University Ghent Belgium.
  • Webber J; Inme Inc. Turku Finland.
  • Hendrix A; Department of Life Technologies Division of Biotechnology University of Turku Turku Finland.
  • Jenster G; Department of Life Technologies Division of Biotechnology University of Turku Turku Finland.
  • Lamminen T; Institute of Life Science 1 Swansea University Medical School Swansea UK.
  • Boström PJ; Laboratory for Experimental Cancer Research Department of Human Structure and Repair Ghent University Ghent Belgium.
  • Pettersson K; Cancer Research Institute Ghent University Ghent Belgium.
  • Lamminmäki U; Department of Urology Erasmus MC Rotterdam The Netherlands.
  • Leivo J; Department of Urology Turku University Hospital and University of Turku Turku Finland.
J Extracell Biol ; 1(10): e64, 2022 Oct.
Article em En | MEDLINE | ID: mdl-38939212
ABSTRACT
Urinary extracellular vesicles (uEVs) are enriched with glycosylated proteins which have been extensively studied as putative biomarkers of urological cancers. Here, we characterized the glycosylation and integrin profile of EVs derived from urological cancer cell lines. We used fluorescent europium-doped nanoparticles coated with lectins and antibodies to identify a biomarker combination consisting of integrin subunit alpha 3 (ITGA3) and fucose. In addition, we used the same cancer cell line-derived EVs as analytical standards to assess the sensitivity of the ITGA3-UEA assay. The clinical performance of the ITGA3-UEA assay was analysed using urine samples of various urological pathologies including diagnostically challenging benign prostatic hyperplasia (BPH), prostate cancer (PCa) and bladder cancer (BlCa). The assay can significantly discriminate BlCa from all other patient groups PCa (9.2-fold; p = 0.00038), BPH (5.5-fold; p = 0.004) and healthy individuals (and 23-fold; p = 0.0001). Our results demonstrate that aberrantly fucosylated uEVs and integrin ITGA3 can be detected with fucose-specific lectin UEA in a simple bioaffinity assay for the detection of BlCa directly from unprocessed urine.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Extracell Biol Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Extracell Biol Ano de publicação: 2022 Tipo de documento: Article