Blocking protein myristoylation inhibits prostate cancer progression

Abstract

Protein N‐myristoylation enables localization to membranes and helps maintain protein conformation and function. N‐myristoyltransferases (NMT) catalyze co‐ or post‐translational myristoylation of Src family kinases and other oncogenic proteins, thereby regulating their function. The goal of this study is 1) to demonstrate that N‐myristoylation is essential for the tumorigenic potential of oncogenioc proteins such as Src kinase; 2) to identify novel lead compounds to inhibit the NMT enzymatic functions; 3) to demonstrate that the compound exhibits its inhibitory function on cancer progression.

Document Details

Document Type
Pub Defense Publication
Publication Date
Apr 01, 2018
Source ID
10.1096/fasebj.2018.32.1_supplement.531.2

Entities

People

  • Houjian Cai
  • Omar Awad Alsaidan
  • Sung Jin Kim

Organizations

  • National Institutes of Health
  • United States Department of Defense
  • University of Georgia

Tags

Readers

  • Breast cancer cell signaling and growth regulation.
  • Molecular Biology and Genetics
  • Molecular and Cellular Biochemistry