Repository logo
 
Publication

Profiling of urinary extracellular vesicle protein signatures from patients with cribriform and intraductal prostate carcinoma in a cross-sectional study

dc.contributor.authorBernardino, R
dc.contributor.authorCarvalho, AS
dc.contributor.authorHall, MJ
dc.contributor.authorAlves, L
dc.contributor.authorLeão, R
dc.contributor.authorSayyid, R
dc.contributor.authorPereira, H
dc.contributor.authorBeck, HC
dc.contributor.authorCampos-Pinheiro, L
dc.contributor.authorHenrique, R
dc.contributor.authorFleshner, N
dc.contributor.authorMatthiesen, R
dc.date.accessioned2024-12-19T00:05:44Z
dc.date.available2024-12-19T00:05:44Z
dc.date.issued2024
dc.description.abstractPrognostic tests and treatment approaches for optimized clinical care of prostatic neoplasms are an unmet need. Prostate cancer (PCa) and derived extracellular vesicles (EVs) proteome changes occur during initiation and progression of the disease. PCa tissue proteome has been previously characterized, but screening of tissue samples constitutes an invasive procedure. Consequently, we focused this study on liquid biopsies, such as urine samples. More specifically, urinary small extracellular vesicle and particles proteome profiles of 100 subjects were analyzed using liquid chromatography coupled to high-resolution mass spectrometry (LC-MS/MS). We identified 171 proteins that were differentially expressed between intraductal prostate cancer/cribriform (IDC/Crib) and non-IDC/non-Crib after correction for multiple testing. However, the strong correlation between IDC/Crib and Gleason Grade complicates the disentanglement of the underlying factors driving this association. Nevertheless, even after accounting for multiple testing and adjusting for ISUP (International Society of Urological Pathology) grading, two proteins continued to exhibit significant differential expression between IDC/Crib and non-IDC/non-Crib. Functional enrichment analysis based on cancer hallmark proteins disclosed a clear pattern of androgen response down-regulation in urinary EVs from IDC/Crib compared to non-IDC/non-Crib. Interestingly, proteome differences between IDC and cribriform were more subtle, suggesting high proteome heterogeneity. Overall, the urinary EV proteome reflected partly the prostate pathology.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationSci Rep . 2024 Oct 23;14(1):25065.pt_PT
dc.identifier.doi10.1038/s41598-024-75272-wpt_PT
dc.identifier.urihttp://hdl.handle.net/10400.26/53264
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.subjectNeoplasias da Prostatapt_PT
dc.subjectVesículas Extracelularespt_PT
dc.subjectBiomarcadores Tumoraispt_PT
dc.subjectProstatic Neoplasmspt_PT
dc.subjectExtracellular Vesiclespt_PT
dc.subjectBiomarkers, Tumorpt_PT
dc.titleProfiling of urinary extracellular vesicle protein signatures from patients with cribriform and intraductal prostate carcinoma in a cross-sectional studypt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.issue1pt_PT
oaire.citation.titleScientific Reportspt_PT
oaire.citation.volume14pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

Files

Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
Scientific Report.pdf
Size:
3.1 MB
Format:
Adobe Portable Document Format
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.85 KB
Format:
Item-specific license agreed upon to submission
Description: