Acquired radioresistance of cancer and the AKT/GSK3β/cyclin D1 overexpression cycle

J Radiat Res. 2011;52(5):539-44. doi: 10.1269/jrr.11098. Epub 2011 Sep 1.

Abstract

Fractionated radiotherapy (RT) is widely used in cancer therapy for its advantages in the preservation of normal tissues. However, repopulation of surviving tumor cells during fractionated RT limits the efficacy of RT. In fact, repopulating tumors often acquire radioresistance and this is the major cause of failure of RT. We have recently demonstrated that human tumor cells acquire radioresistance when exposed to fractionated radiation (FR) of X-rays every 12 hours for 1 month. The acquired radioresistance was associated with overexpression of cyclin D1, a result of a series of molecular changes; constitutive activation of DNA-PK and AKT with concomitant down-regulation of glycogen synthase kinase-3β (GSK3β) which results in suppression of cyclin D1 proteolysis. Aberrant cyclin D1 overexpression in S-phase induced DNA double strand breaks which activated DNA-PK and established the vicious cycle of cycling D1 overexpression. This overexpression of cyclin D1 is responsible for the radioresistance phenotype of long-term FR cells, since this phenotype was completely abrogated by treatment of FR cells by the API-2, an AKT inhibitor or by a Cdk4 inhibitor. Thus, targeting the AKT/GSK3β/cyclin D1/Cdk4 pathway can be an efficient modality to suppress acquired radioresistance of tumor cells. In this article, I overview the newly discovered molecular mechanisms underlying acquired radioresistance of tumor cells induced by FR, and propose a strategy for eradication of tumors using fractionated RT by overcoming tumor radioresistance.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Awards and Prizes
  • Cyclin D1 / metabolism*
  • Cyclin-Dependent Kinase 4 / antagonists & inhibitors
  • Cyclin-Dependent Kinase 4 / metabolism
  • Dose Fractionation, Radiation
  • Feedback, Physiological
  • G1 Phase Cell Cycle Checkpoints / radiation effects
  • Glycogen Synthase Kinase 3 / metabolism*
  • Glycogen Synthase Kinase 3 beta
  • Humans
  • Neoplasms / drug therapy
  • Neoplasms / metabolism*
  • Neoplasms / radiotherapy*
  • Nucleosides / pharmacology
  • Oncogene Protein v-akt / antagonists & inhibitors
  • Oncogene Protein v-akt / metabolism*
  • Protein Kinase Inhibitors / pharmacology
  • Pyridazines / pharmacology
  • Radiation Tolerance* / drug effects
  • Radiation Tolerance* / physiology
  • Signal Transduction / drug effects
  • Signal Transduction / radiation effects
  • Treatment Failure

Substances

  • API-2 nucleoside
  • CCND1 protein, human
  • Nucleosides
  • Protein Kinase Inhibitors
  • Pyridazines
  • Cyclin D1
  • GSK3B protein, human
  • Glycogen Synthase Kinase 3 beta
  • Oncogene Protein v-akt
  • CDK4 protein, human
  • Cyclin-Dependent Kinase 4
  • Glycogen Synthase Kinase 3