The Importance of Autophagy in Breast Cancer Development and Treatment

Abstract

During this grant period, we found that growth factor inhibitors as well as nutrient depletion activated autophagy in human beast cancer cells, and the increased activity of autophagy was associated with a decrease in cellular ATP and an increase in activities of AMP kinase and eEF-2 kinase. Silencing of eEF-2 kinase relieved the inhibition of protein synthesis, led to a greater reduction of cellular ATP, and blunted autophagic response. We further demonstrated that suppression of eEF-2 kinase-regulated autophagy impeded cell growth in serum/nutrient-deprived cultures and handicapped cell survival, and enhanced the efficacy of the growth factor inhibitors such as trastuzumab, gefitinib, and lapatinib. The results of this study provide new evidence that activation of eEF 2 kinase-mediated autophagy plays a protective role for cancer cells under metabolic stress conditions, and that targeting autophagic survival may represent a novel approach to enhancing the effectiveness of growth factor inhibitors such as trastuzumab, gefitinib, and lapatinib .

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Document Details

Document Type
Technical Report
Publication Date
Mar 01, 2010
Accession Number
ADA525625

Entities

People

  • Jin-ming Yang

Organizations

  • Pennsylvania State University

Tags

DTIC Thesaurus Topics

  • Autophagy
  • Biomedical Research
  • Breast Cancer
  • Cancer
  • Cells
  • Deprivation
  • Elongation
  • Growth Factors
  • Inhibition
  • Inhibitors
  • Kinases
  • Neoplasms
  • Phosphorylation
  • Stress (Physiology)
  • Survival
  • Targeting
  • Tumor Cell Line

Fields of Study

  • Biology
  • Chemistry
  • Medicine

Readers

  • Cellular and Molecular Pathways of Apoptosis.
  • Oncology (Cancer Research).