4.8 Article

Detection of early prostate cancer using a hepsin-targeted imaging agent

Journal

CANCER RESEARCH
Volume 68, Issue 7, Pages 2286-2291

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/0008-5472.CAN-07-1349

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Funding

  1. NCI NIH HHS [R24-CA92782, P50 CA086355-03, U54 CA119349, U54 CA119349-040003, P50-CA090381, P50 CA090381, U54-CA119349, R24 CA092782-05, P50 CA086355, R24 CA092782, P50-CA86355] Funding Source: Medline
  2. NIA NIH HHS [R01AG21404, R01 AG021404] Funding Source: Medline

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Early detection and diagnosis of prostate cancer is key to designing effective treatment strategies. Microarrays have resulted in the discovery of hepsin (HPN) as a biomarker for detection of prostate cancer. In this study, we explore the development of HPN imaging probes for detection of prostate cancer. We used phage display to isolate HPN binding peptides with 190 + 2.2 nmol/L affinity in monomeric form and high specificity. The identified peptides were able to detect human prostate cancer on tissue microarrays and in cell-based assays. HPN-targeted imaging agents were synthesized by conjugating multiple peptides to fluorescent nanoparticles to further improve avidity through multivalency and to improve pharmacokinetics. When injected into mouse xenograft models, RPN-targeted nanoparticles bound specifically to RPN-expressing LNCaP xenografts compared with non-HPN-expressing PC3 xenografts. HpN imaging may provide a new method for detection of prostate cancer.

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