Crosstalk between autophagy and intracellular radiation response (Review)

Int J Oncol. 2016 Dec;49(6):2217-2226. doi: 10.3892/ijo.2016.3719. Epub 2016 Oct 5.

Abstract

Autophagy induced by radiation is critical to cell fate decision. Evidence now sheds light on the importance of autophagy induced by cancer radiotherapy. Traditional view considers radiation can directly or indirectly damage DNA which can activate DNA damage the repair signaling pathway, a large number of proteins participating in DNA damage repair signaling pathway such as p53, ATM, PARP1, FOXO3a, mTOR and SIRT1 involved in autophagy regulation. However, emerging recent evidence suggests radiation can also cause injury to extranuclear targets such as plasma membrane, mitochondria and endoplasmic reticulum (ER) and induce accumulation of ceramide, ROS, and Ca2+ concentration which activate many signaling pathways to modulate autophagy. Herein we review the role of autophagy in radiation therapy and the potent intracellular autophagic triggers induced by radiation. We aim to provide a more theoretical basis of radiation-induced autophagy, and provide novel targets for developing cytotoxic drugs to increase radiosensitivity.

Publication types

  • Review

MeSH terms

  • Autophagy / radiation effects*
  • DNA Damage / genetics
  • DNA Damage / radiation effects
  • DNA Repair / genetics
  • DNA Repair / radiation effects
  • Endoplasmic Reticulum / pathology
  • Endoplasmic Reticulum / radiation effects*
  • Endoplasmic Reticulum Stress / radiation effects*
  • Humans
  • Mitochondria / pathology
  • Mitochondria / radiation effects*
  • Neoplasms / genetics
  • Neoplasms / radiotherapy*
  • Reactive Oxygen Species / metabolism

Substances

  • Reactive Oxygen Species