Developing Novel Therapeutics Targeting Undifferentiated and Castration-Resistant Prostate Cancer Stem Cells

Abstract

The main objective of this DOD-supported project is to identify and develop novel therapeutics to target the undifferentiated (PSA-/lo), castration-resistant PCSCs. We proposed to achieve this objective with two Specific Aims: 1) To perform phage display library (PDL) screening in PSA-/lo PCa cells to identify PCSC-specific homing peptides; and 2) To perform unbiased drug library screening to identify novel PCSC-targeting chemicals. In the past year, we have made good progress in accomplishing the goals for both Aims. For Specific Aim 1, we have further characterized the JRM2 peptide. For Specific Aim 2, we have finished a targeted library screening to identify several compounds that could sensitize the AR-PSA- LNCaP cells. We have also started screening our UNIQUE PSA-/lo CRPC cells against a Protein Kinase Inhibitor Collection that contains >750 compounds that target >140 kinases. In the second year, we shall continue several experiments in both Aims, especially testing the in vitro and in vivo cytotoxicities of the conjugated JRM2 peptide and finishing up screening and validating the kinase inhibitor library screening.

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Document Details

Document Type
Technical Report
Publication Date
Oct 01, 2015
Accession Number
AD1004100

Entities

People

  • Dean Tang

Organizations

  • The University of Texas MD Anderson Cancer Center

Tags

DTIC Thesaurus Topics

  • Bacteriophages
  • Biomedical Research
  • Castration
  • Cell Physiological Processes
  • Cells
  • Confocal Microscopy
  • Department Of Defense
  • Inhibitors
  • Medical Personnel
  • Molecules
  • Neoplasms
  • Prostate Cancer
  • Proteins
  • Stem Cells
  • Targeting
  • Targets
  • Therapy

Fields of Study

  • Biology
  • Chemistry

Readers

  • Molecular Genetics
  • Prostate Cancer Biology.
  • Research Science/Academic Research

Technology Areas

  • Biotechnology
  • Biotechnology - Cancer Biotech