Functional Characterization of eRNA-Coregulator Interactions at AR-Bound Enhancers in Advanced Therapy-Resistant Prostate Cancer

Abstract

Prostate cancer (PCa) which has relapsed after first line androgen deprivation therapy (ADT),known as ADT-Recurrent PCa (ADT-RPCa) is incurable and the lethal form of the disease. Second generation antiandrogens, such as enzalutamide and apalutamide, are often used to treat ADTRPCa but resistance to these drugs emerges within several months. Disease progression and the acquisition of therapy resistance in PCa is associated with changes in binding of the androgen receptor (AR) to its cis-regulatory enhancer elements. Enhancers, which regulate the rate of transcription by serving as nucleation sites for the binding of transcription factors, coregulators, RNA polymerase II and other regulatory proteins, were recently found to be transcribed, producing non-coding RNA molecules called enhancer RNA (eRNA) which are increasingly being recognized for their role in enhancer function. While eRNAs have been shown to be transcribed from critical AR-bound active enhancers, their role in AR-regulated gene expression and PCa progression remains largely unknown.

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Document Details

Document Type
Technical Report
Publication Date
Mar 01, 2023
Accession Number
AD1202189

Entities

People

  • Rayzel Fernandes

Organizations

  • Imperial College London

Tags

DTIC Thesaurus Topics

  • Acquisition
  • Androgen Receptors
  • Androgens
  • Biology
  • Biomedical Research
  • Cancer
  • Cell Line
  • Cells
  • Chemical Compounds
  • Chemistry
  • Computational Biology
  • Data Sets
  • Diseases
  • Gene Expression
  • Hormones
  • Macromolecules
  • Medical Personnel
  • Molecular Biology
  • Neoplasms
  • Prostate
  • Prostate Cancer
  • Proteins
  • Resistance
  • United Kingdom

Fields of Study

  • Biology

Readers

  • Molecular Genetics
  • Oncology
  • Prostate Cancer Biology.