[Frontiers in Bioscience E2, 641-656, January 1, 2010]

Molecular markers for prostatic cancer

Tommaso Castelli, Sebastiano Cimino, Carlo Magno, Giuseppe Morgia

Department of Urology, University of Messina, Consolare Valeria Avenue, 98100 Messina, Italy

TABLE OF CONTENTS

1. Abstract
2. Introduction
3. Prostate specific antigen (PSA), PSA isoforms and PSA derivates
4. Human glandular kallikrein 2 (hK2)
5. DNA Biomarkers
5.1. Epigenetic markers
5.2. Gene fusion/translocation markers
6. RNA biomarkers
6.1. PCA3
6.2. Alpha-methylacyl CoA Racemase
7. Prostate antigens
7.1. Prostate-specific membrane antigen
7.2. Early prostate cancer antigens
8. Proteomics
9. Serum neuroendocrine markers in prostate cancer
9.1. Chromogranin A (CGA)
9.2. Neuron Specific Enolase (NSE)
9.3. Pro gastrin releasing peptide (Pro GRP)
10. Future perspective
11. Acknowledgment
12. References

1. ABSTRACT

Prostate cancer (caP) is a major public health problem. Many groups have attempted to identify prognostic risk factors to early detect caP and to identify who will need active treatment. Since the introduction of prostate specific antigen (PSA), diagnosis of caP has increased even as mortality for prostatic cancer has declined. Using current recommended guidelines, the PSA test suffers from both of limited specificity and sensitivity. With the aim to improve early detection of prostatic cancer the volume adjusted PSA, PSA isoforms and PSA kinetics have been investigated. Recently, technological advances in molecular assays have led to the discovery of new markers with high specificity. Further, proteomic array profiling and DNA methylation assays could provide for more accurate diagnosis and prognosis. Current evidence suggests that no single marker is likely to achieve the desired level of diagnostic and prognostic accuracy: future research should focus on validation of already existing biomarkers and the discovery of new markers to identify men with aggressive prostate cancer and to predict outcomes after therapies.