Novel molecular targets for kRAS downregulation: promoter G-quadruplexes

Abstract

The aim of this project was to characterize the biologically relevant non-canonical G-quadruplex (G4) structure within the promoter of the kRAS oncogene, and to determine the transcriptional regulation of the kRAS gene, particularly as it relates to the G4-forming region(s). Throughout the proposal, we elucidated a predominant G4 structure within the mid-G4-forming region of the promoter under varying co-solvent and nucleoplasm conditions, and described the structure as having mixed parallel/anti-parallel loops of lengths 2:8:10 in the 5-3 direction. Using selective small molecules for the mid- and near-G4 regions, we further supported the ideal target for therapeutic development to be the mid-region structure. In support of aim 2, we examined the binding and functional effects of transcription factors predicted to bind to the G4-forming regions Sp1, MAZ, and p53. While some of these silenced transcription, we expanded our search for activators to the entire promoter, examined the effects of E2F, AP1 and PPAR-gamma and searched for more interactive agents by LC-MS/MS.

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Document Details

Document Type
Technical Report
Publication Date
Nov 01, 2016
Accession Number
AD1039525

Entities

People

  • Tracy A Brooks

Organizations

  • University of Mississippi

Tags

DTIC Thesaurus Topics

  • Cancer
  • Cell Line
  • Chemical Synthesis
  • Chemistry
  • Chromosome Structures
  • Colon Cancer
  • Energy Transfer
  • Genetics
  • Health Services
  • Molecules
  • Neoplasms
  • Nucleic Acids
  • Organic Chemistry
  • Proteins
  • Small Molecules
  • Therapy
  • Transcription Factors

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