Increased Plasmatic Levels of PSA-Expressing Exosomes Distinguish Prostate Cancer Patients from Benign Prostatic Hyperplasia: A Prospective Study.
Mariantonia LogozziDaniela Francesca AngeliniAlessandro GiulianiDavide MizzoniRossella Di RaimoMartina MaggiAlessandro GentilucciVittorio MarzioStefano SalcicciaGiovanna BorsellinoLuca BattistiniAlessandro SciarraStefano FaisPublished in: Cancers (2019)
Prostate Specific Antigen (PSA) fails to discriminate between benign prostatic hyperplasia (BPH) and Prostate Cancer (PCa), resulting in large numbers of unnecessary biopsies and missed cancer diagnoses. Nanovesicles called exosomes are directly detectable in patient plasma and here we explore the potential use of plasmatic exosomes expressing PSA (Exo-PSA) in distinguishing healthy individuals, BPH, and PCa. Exosomes were obtained from plasma samples of 80 PCa, 80 BPH, and 80 healthy donors (CTR). Nanoparticle Tracking Analysis (NTA), immunocapture-based ELISA (IC-ELISA), and nanoscale flow-cytometry (NSFC), were exploited to detect and characterize plasmatic exosomes. Statistical analysis showed that plasmatic exosomes expressing both CD81 and PSA were significantly higher in PCa as compared to both BPH and CTR, reaching 100% specificity and sensitivity in distinguishing PCa patients from healthy individuals. IC-ELISA, NSFC, and Exo-PSA consensus score (EXOMIX) showed 98% to 100% specificity and sensitivity for BPH-PCa discrimination. This study outperforms the conventional PSA test with a minimally invasive widely exploitable approach.
Keyphrases
- benign prostatic hyperplasia
- prostate cancer
- lower urinary tract symptoms
- mesenchymal stem cells
- radical prostatectomy
- stem cells
- minimally invasive
- flow cytometry
- end stage renal disease
- ejection fraction
- bone marrow
- chronic kidney disease
- case report
- monoclonal antibody
- mass spectrometry
- climate change
- risk assessment
- squamous cell
- human health