Abstract

Prostate-specific antigen (PSA), a kallikrein isolated by Wang in 1979 [1], is a physiologic excretory product of the healthy prostatic epithelium, involved in the semen liquefaction process. A small amount of PSA (less than 1 molecule per million excreted) leaks into the bloodstream where its normal level was – arbritarily – fixed more than 2 decades ago at 4 ng/ml and shown to rise in any prostatic pathologic condition associated with alterations of the basement membrane: prostatitis, benign prostatic hypertrophy (BPH) and, of course, cancer. While definitely not a tumor marker, PSA has been used and approved as a marker for the detection of prostate cancer [1] and therefore, extensively promoted as the marker for early detection and eventually, screening. This has induced an unprecedented revolution in urology and oncology, leading to a spectacular increase in the incidence of prostate cancer, inducing a dramatic expansion of surgery and radiation therapy without any spectacular modification of the prostate cancer death rate up to this point in time. However, once initially seen as a ‘magic bullet’, PSA is increasingly confronting clinicians with more questions than they seem able to answer, which this editorial will try to summarize.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.