A novel response of cancer cells to radiation involves autophagy and formation of acidic vesicles

Cancer Res. 2001 Jan 15;61(2):439-44.

Abstract

The mechanisms underlying neoplastic epithelial cell killing by ionizing radiation are largely unknown. We discovered a novel response to radiation manifested by autophagy and the development of acidic vesicular organelles (AVO). Acidification of AVO was mediated by the vacuolar H+-ATPase. Staining with the lysosomotropic agent acridine orange enabled us to quantify AVO accumulation and to demonstrate their time- and dose-dependent appearance. The appearance of AVO occurred in the presence of the pan-caspase inhibitor z-Val-Ala-Asp(Ome)-fluoromethyl ketone, but was inhibited by 3-methyladenine, an inhibitor of autophagy. The accretion of AVO in surviving progenies of irradiated cells, and the increased incidence of clonogenic death after inhibition of vacuolar H+-ATPase suggest that formation of acidic organelles represents a novel defense mechanism against radiation damage.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenine / analogs & derivatives
  • Adenine / pharmacology
  • Autophagy / radiation effects*
  • Cytoplasmic Vesicles / drug effects
  • Cytoplasmic Vesicles / radiation effects*
  • Cytoplasmic Vesicles / ultrastructure
  • DNA, Neoplasm / genetics
  • DNA, Neoplasm / radiation effects
  • Dose-Response Relationship, Radiation
  • Humans
  • Hydrogen-Ion Concentration
  • Microscopy, Electron
  • Proton-Translocating ATPases / metabolism
  • Time Factors
  • Tumor Cells, Cultured / drug effects
  • Tumor Cells, Cultured / radiation effects
  • Tumor Cells, Cultured / ultrastructure
  • Vacuolar Proton-Translocating ATPases*

Substances

  • DNA, Neoplasm
  • 3-methyladenine
  • Vacuolar Proton-Translocating ATPases
  • Proton-Translocating ATPases
  • Adenine