Proteomic profiling of ectosomes derived from paired urothelial bladder cancer and normal cells reveals the presence of biologically-relevant molecules
Proteomic profiling of ectosomes derived from paired urothelial bladder cancer and normal cells reveals the presence of biologically-relevant molecules
Proteomic profiling of ectosomes derived from paired urothelial bladder cancer and normal cells reveals the presence of biologically-relevant molecules
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dc.type
JournalArticle
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dc.abstract.en
Protein content of extracellular vesicles (EVs) can modulate different processes during carcinogenesis. Novel proteomic strategies have been applied several times to profile proteins present in exosomes released by urothelial bladder cancer (UBC) cells. However, similar studies have not been conducted so far on another population of EVs, i.e., ectosomes. In the present study we used a shotgun nanoLC–MS/MS proteomic approach to investigate the protein content of ectosomes released in vitro by T-24 UBC cells and HCV-29 normal ureter epithelial cells. In addition, cancer-promoting effects exerted by UBC-derived ectosomes on non-invasive cells in terms of cell proliferation and migratory properties were assessed. In total, 1158 proteins were identified in T-24-derived ectosomes, while HCV-29-derived ectosomes contained a lower number of 259 identified proteins. Qualitative analysis revealed 938 proteins present uniquely in T-24-derived ectosomes, suggesting their potential applications in bladder cancer management as diagnostic and prognostic biomarkers. In addition, T-24-derived ectosomes increased proliferation and motility of recipient cells, likely due to the ectosomal transfer of the identified cancer-promoting molecules. The present study provided a focused identification of biologically relevant proteins in UBC-derived ectosomes, confirming their role in UBC development and progression, and their applicability for further biomarker-oriented studies in preclinical or clinical settings.
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dc.subject.en
biomarkers
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dc.subject.en
bladder cancer
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dc.subject.en
ectosomes
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extracellular vesicles
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dc.subject.en
nanoLC-MS/MS
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mass spectrometry
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dc.subject.en
proteomics
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dc.description.volume
22
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dc.description.number
13
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dc.identifier.doi
10.3390/ijms22136816
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dc.identifier.eissn
1422-0067
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dc.title.journal
International Journal of Molecular Sciences
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dc.language.container
eng
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dc.affiliation
Wydział Biologii : Instytut Zoologii i Badań Biomedycznych
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dc.affiliation
Wydział Fizyki, Astronomii i Informatyki Stosowanej : Instytut Fizyki im. Mariana Smoluchowskiego
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dc.affiliation
Wydział Biochemii, Biofizyki i Biotechnologii : Zakład Biochemii Fizycznej
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dc.affiliation
Pion Prorektora ds. badań naukowych : Małopolskie Centrum Biotechnologii
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dc.affiliation
Jagiellonian Interdisciplinary PhD Programme
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dc.subtype
Article
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dc.identifier.articleid
6816
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dc.rights.original
CC-BY; otwarte czasopismo; ostateczna wersja wydawcy; w momencie opublikowania; 0