Over the past five years we have investigated the biochemical and molecular aspects of hK2 and its proform (phK2) and have developed highly sensitive and specific analytic assays for these biomarkers. Our studies have shown that these proteins are localized predominately in the prostate, are hormonally regulated and have potential proteolytic role in the activation of PSA from proPSA. Preliminary studies also have shown that the ratio of serum concentration of hK2 to free-PSA is useful for identifying those patients with borderline elevated PSA concentrations who are most likely to have prostate cancer.
Specific Aim 1 will employ the proven molecular, biochemical and analytic techniques used to characterize and measure hK2 to further characterize and develop assays for three new prostate cancer markers: inhibitor - 6 complex (hK2-PI6), hK2 variant (hK2-v) and PSA variant (PSA-v). Vectors will be developed to produce recombinant forms of these proteins and specific monoclonal antibodies will be produced. These antibodies will be used for purification of endogenous proteins, immunohistochemistry studies and development of sensitive and specific immunoassays.
Specific Aim 2 involves a collaboration with clinical colleagues in Urology, Oncology and the Cancer Center. Blood, tissue and clinical follow-up information will be collected for three large cohorts of patients. One cohort will include 3000 men undergoing transrectal needle biopsy of the prostate. Another cohort will include 300 men with rising PSA concentrations and negative needle biopsy undergoing saturation biopsy of the prostate under anesthesia. A third cohort will include 240 men with advanced hormone refractory prostate cancer. Each of these cohorts will have PSA, free PSA, hK2 and phK2 measured in their blood to determine the utility of these markers for improving cancer detection and predicting outcomes. In addition, cancer prediction algorithms will be validated with blood from 600 Asian men from Korea undergoing prostate biopsy. Aliquots of blood from the cohorts also will be held frozen to evaluate the utility of hK2-PI6, hK2-v and PSA-v once assays have been developed. The major goal of these studies will be the development of the most practical and accurate assays to improve the detection, diagnosis and management of prostate cancer.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Specialized Center (P50)
Project #
5P50CA091956-02
Application #
6641458
Study Section
Special Emphasis Panel (ZCA1)
Project Start
2002-08-01
Project End
2003-07-31
Budget Start
Budget End
Support Year
2
Fiscal Year
2002
Total Cost
Indirect Cost
Name
Mayo Clinic, Rochester
Department
Type
DUNS #
City
Rochester
State
MN
Country
United States
Zip Code
55905
Guerrico, Anatilde Gonzalez; Hillman, David; Karnes, Jeffery et al. (2017) Roles of kallikrein-2 biomarkers (free-hK2 and pro-hK2) for predicting prostate cancer progression-free survival. J Circ Biomark 6:1849454417720151
Hearn, Jason W D; AbuAli, Ghada; Reichard, Chad A et al. (2016) HSD3B1 and resistance to androgen-deprivation therapy in prostate cancer: a retrospective, multicohort study. Lancet Oncol 17:1435-1444
Spratt, Daniel E; Evans, Michael J; Davis, Brian J et al. (2015) Androgen Receptor Upregulation Mediates Radioresistance after Ionizing Radiation. Cancer Res 75:4688-96
Lu, Ji; Lonergan, Peter E; Nacusi, Lucas P et al. (2015) The cistrome and gene signature of androgen receptor splice variants in castration resistant prostate cancer cells. J Urol 193:690-8
Urban, Matthew W; Wang, Chenyi; Alizad, Azra et al. (2015) Complex background suppression for vibro-acoustography images. Ultrasonics 56:456-72
Cooperberg, Matthew R; Davicioni, Elai; Crisan, Anamaria et al. (2015) Combined value of validated clinical and genomic risk stratification tools for predicting prostate cancer mortality in a high-risk prostatectomy cohort. Eur Urol 67:326-33
Alshalalfa, Mohammed; Crisan, Anamaria; Vergara, Ismael A et al. (2015) Clinical and genomic analysis of metastatic prostate cancer progression with a background of postoperative biochemical recurrence. BJU Int 116:556-67
Loeb, Stacy; Sanda, Martin G; Broyles, Dennis L et al. (2015) The prostate health index selectively identifies clinically significant prostate cancer. J Urol 193:1163-9
Ahmed, Kamran A; Davis, Brian J; Mynderse, Lance A et al. (2014) Comparison of biochemical failure rates between permanent prostate brachytherapy and radical retropubic prostatectomy as a function of posttherapy PSA nadir plus 'X'. Radiat Oncol 9:171
Wu, Qiang; Kohli, Manish; Bergen 3rd, H Robert et al. (2014) Preclinical evaluation of the supercritical extract of azadirachta indica (neem) leaves in vitro and in vivo on inhibition of prostate cancer tumor growth. Mol Cancer Ther 13:1067-77

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