Combinational Targeting EZH2 and PARP1 in Prostate Cancer

Abstract

Most advanced prostate cancer cells have higher levels of EZH2 and PARP1 proteins compared to that in early stage prostate cancer cells, suggesting the importance of these proteins in prostate cancer progression. We found that PARP1 directly interacts with EZH2. In the proposed project, we will identify precisely how EZH2 and PARP1 interact and how these two proteins regulate each other in prostate cancer. Next, we will study how EZH2 and PARP1 work together to decrease the expression of tumor suppressors (genes/proteins that inhibit tumor growth) and increase genetic instability in advanced prostate cancer. Understanding these mechanisms will lead to the future design of new inhibitors of EZH2 and PARP1. Furthermore, our preliminary data strongly suggest that PARP inhibition-resistant tumors have higher levels of EZH2 compared to PARP inhibition-sensitive tumors and that inhibiting EZH2 alone enhances the enzymatic activities of PARPs; thus, overcoming the therapeutic effectiveness of PARP inhibition. Therefore, our work provides a novel rationale to target both PARPs and EZH2, and we predict that the inhibition of both PARPs and EZH2 will kill more cancer cells than inhibiting either PARPs or EZH2 alone. We anticipate that this combination therapy will overcome therapeutic resistance and will substantially benefit the majority of prostate cancer patients, regardless of any DNA repair defects.

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Document Details

Document Type
Technical Report
Publication Date
Sep 01, 2018
Accession Number
AD1095998

Entities

People

  • Qi Cao

Organizations

  • Houston Methodist Research Institute

Tags

DTIC Thesaurus Topics

  • Biomedical Research
  • Cell Line
  • Combination Therapy
  • Department Of Defense
  • Diseases And Disorders
  • Health Services
  • Inhibition
  • Inhibitors
  • Local Governments
  • Medical Personnel
  • Neoplasms
  • Professional Development
  • Prostate
  • Prostate Cancer
  • Targeting
  • Targets
  • Therapy

Fields of Study

  • Biology
  • Medicine

Readers

  • Molecular Biology and Genetics
  • Oncology (Cancer Research).

Technology Areas

  • Biotechnology