TY - JOUR
T1 - The role of proteomics in prostate cancer research
T2 - Biomarker discovery and validation
AU - Pin, Elisa
AU - Fredolini, Claudia
AU - Petricoin, Emanuel F.
N1 - Funding Information:
This work has been supported by the Italian Istituto Superiore di Sanita in the framework of the Italy/USA cooperation agreement between the US Department of Health and Human Services , George Mason University , and the Italian Ministry of Public Health , as well as the generous support of the College of Science, George Mason University .
PY - 2013/4
Y1 - 2013/4
N2 - Purpose: Prostate Cancer (PCa) represents the second most frequent type of tumor in men worldwide. Incidence increases with patient age and represents the most important risk factor. PCa is mostly characterized by indolence, however in a small percentage of cases (3%) the disease progresses to a metastatic state. To date, the most important issue concerning PCa research is the difficulty in distinguishing indolent from aggressive disease. This problem frequently results in low-grade PCa patient overtreatment and, in parallel; an effective treatment for distant and aggressive disease is not yet available. Result: Proteomics represents a promising approach for the discovery of new biomarkers able to improve the management of PCa patients. Markers more specific and sensitive than PSA are needed for PCa diagnosis, prognosis and response to treatment. Moreover, proteomics could represent an important tool to identify new molecular targets for PCa tailored therapy. Several possible PCa biomarkers sources, each with advantages and limitations, are under investigation, including tissues, urine, serum, plasma and prostatic fluids. Innovative high-throughput proteomic platforms are now identifying and quantifying new specific and sensitive biomarkers for PCa detection, stratification and treatment. Nevertheless, many putative biomarkers are still far from being applied in clinical practice. Conclusions: This review aims to discuss the recent advances in PCa proteomics, emphasizing biomarker discovery and their application to clinical utility for diagnosis and patient stratification.
AB - Purpose: Prostate Cancer (PCa) represents the second most frequent type of tumor in men worldwide. Incidence increases with patient age and represents the most important risk factor. PCa is mostly characterized by indolence, however in a small percentage of cases (3%) the disease progresses to a metastatic state. To date, the most important issue concerning PCa research is the difficulty in distinguishing indolent from aggressive disease. This problem frequently results in low-grade PCa patient overtreatment and, in parallel; an effective treatment for distant and aggressive disease is not yet available. Result: Proteomics represents a promising approach for the discovery of new biomarkers able to improve the management of PCa patients. Markers more specific and sensitive than PSA are needed for PCa diagnosis, prognosis and response to treatment. Moreover, proteomics could represent an important tool to identify new molecular targets for PCa tailored therapy. Several possible PCa biomarkers sources, each with advantages and limitations, are under investigation, including tissues, urine, serum, plasma and prostatic fluids. Innovative high-throughput proteomic platforms are now identifying and quantifying new specific and sensitive biomarkers for PCa detection, stratification and treatment. Nevertheless, many putative biomarkers are still far from being applied in clinical practice. Conclusions: This review aims to discuss the recent advances in PCa proteomics, emphasizing biomarker discovery and their application to clinical utility for diagnosis and patient stratification.
KW - Biomarkers
KW - Body fluids
KW - Diagnosis
KW - Prognosis
KW - Prostate cancer
KW - Proteomics
KW - Tissues
KW - Treatment
UR - http://www.scopus.com/inward/record.url?scp=84891722548&partnerID=8YFLogxK
U2 - 10.1016/j.clinbiochem.2012.12.012
DO - 10.1016/j.clinbiochem.2012.12.012
M3 - Article
C2 - 23266295
AN - SCOPUS:84891722548
SN - 0009-9120
VL - 46
SP - 524
EP - 538
JO - Clinical Biochemistry
JF - Clinical Biochemistry
IS - 6
ER -