Quiescence and attenuated DNA damage response promote survival of esophageal cancer stem cells

J Cell Biochem. 2012 Dec;113(12):3643-52. doi: 10.1002/jcb.24228.

Abstract

Accumulating evidence indicates cancer stem cells (CSCs) possess the capability to resist DNA-damage induced cell death, whereas the mechanism is largely unknown. Here we show that cell cycle status and DNA damage response (DDR) in CSCs probably contribute to their survival in genotoxic insults. In this study, we isolated esophageal cancer stem cells (ECSCs) from esophageal cancer cell line EC9706 by side-population (SP) phenotype through flow cytometry and found that ECSCs preferentially stay quiescent as compared to the non-ECSCs and are more resistant to DNA damage agents. Further study revealed that ECSCs express a lower level of EGFR, phosphoralated Stat3, and c-Myc, yet abnormally upregulated p27. More interestingly, different from non-ECSCs, when suffering DNA damage agents, ECSCs showed attenuated DDR, as well as declined DNA repair potential. These data indicated ECSCs probably employed an impaired DDR to handle severe genomic insults. Conclusively, we infer that the damage-resistance ability of ECSCs is likely attributed to their slow-cycling status and avoidance of apoptosis or senescence triggered by an excessive DDR.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis
  • Benzimidazoles
  • Cell Line, Tumor
  • Cell Survival
  • Cisplatin / pharmacology
  • Coculture Techniques
  • DNA Damage*
  • DNA Repair*
  • DNA, Neoplasm / analysis*
  • DNA, Neoplasm / genetics
  • Drug Resistance, Neoplasm
  • ErbB Receptors / genetics
  • ErbB Receptors / metabolism
  • Esophageal Neoplasms / genetics
  • Esophageal Neoplasms / pathology*
  • Flow Cytometry
  • G1 Phase Cell Cycle Checkpoints
  • Gene Expression Regulation, Neoplastic
  • Genes, myc
  • Humans
  • Mutagenicity Tests / methods
  • Neoplastic Stem Cells / drug effects
  • Neoplastic Stem Cells / pathology*
  • Phenotype
  • Phosphorylation
  • STAT3 Transcription Factor / genetics
  • STAT3 Transcription Factor / metabolism
  • Tumor Stem Cell Assay
  • Ultraviolet Rays

Substances

  • Benzimidazoles
  • DNA, Neoplasm
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • EGFR protein, human
  • ErbB Receptors
  • bisbenzimide ethoxide trihydrochloride
  • Cisplatin