| Literature DB >> 33922033 |
Stefano Salciccia1, Anna Laura Capriotti2, Aldo Laganà2, Stefano Fais3, Mariantonia Logozzi3, Ettore De Berardinis1, Gian Maria Busetto4, Giovanni Battista Di Pierro1, Gian Piero Ricciuti1, Francesco Del Giudice1, Alessandro Sciarra1, Peter R Carroll5, Matthew R Cooperberg5, Beatrice Sciarra2, Martina Maggi1.
Abstract
Early detection of prostate cancer (PC) is largely carried out using assessment of prostate-specific antigen (PSA) level; yet it cannot reliably discriminate between benign pathologies and clinically significant forms of PC. To overcome the current limitations of PSA, new urinary and serum biomarkers have been developed in recent years. Although several biomarkers have been explored in various scenarios and patient settings, to date, specific guidelines with a high level of evidence on the use of these markers are lacking. Recent advances in metabolomic, genomics, and proteomics have made new potential biomarkers available. A number of studies focused on the characterization of the specific PC metabolic phenotype using different experimental approaches has been recently reported; yet, to date, research on metabolomic application for PC has focused on a small group of metabolites that have been known to be related to the prostate gland. Exosomes are extracellular vesicles that are secreted from all mammalian cells and virtually detected in all bio-fluids, thus allowing their use as tumor biomarkers. Thanks to a general improvement of the technical equipment to analyze exosomes, we are able to obtain reliable quantitative and qualitative information useful for clinical application. Although some pilot clinical investigations have proposed potential PC biomarkers, data are still preliminary and non-conclusive.Entities:
Keywords: biomarkers; early diagnosis; exosomes; metabolomics; prostate cancer
Year: 2021 PMID: 33922033 DOI: 10.3390/ijms22094367
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923