Transforming doxorubicin into a cancer stem cell killer via EpCAM aptamer-mediated delivery

Theranostics. 2017 Sep 20;7(17):4071-4086. doi: 10.7150/thno.20168. eCollection 2017.

Abstract

Chemotherapy-resistant cancer stem cells (CSCs) are a major obstacle to the effective treatment of many forms of cancer. To overcome CSC chemo-resistance, we developed a novel system by conjugating a CSC-targeting EpCAM aptamer with doxorubicin (Apt-DOX) to eliminate CSCs. Incubation of Apt-DOX with colorectal cancer cells resulted in high concentration and prolonged retention of DOX in the nuclei. Treatment of tumour-bearing xenograft mice with Apt-DOX resulted in at least 3-fold more inhibition of tumour growth and longer survival as well as a 30-fold lower frequency of CSC and a prolonged longer tumourigenic latency compared with those receiving the same dose of free DOX. Our data demonstrate that a CSC-targeting aptamer is able to transform a conventional chemotherapeutic agent into a CSC-killer to overcome drug resistance in solid tumours.

Keywords: cancer stem cell killer; doxorubicin.

MeSH terms

  • Animals
  • Antibiotics, Antineoplastic / administration & dosage
  • Antibiotics, Antineoplastic / chemistry
  • Aptamers, Nucleotide / administration & dosage*
  • Dose-Response Relationship, Drug
  • Doxorubicin / administration & dosage*
  • Doxorubicin / chemistry
  • Drug Carriers / administration & dosage
  • Drug Carriers / chemistry
  • Drug Delivery Systems / methods*
  • Epithelial Cell Adhesion Molecule / genetics*
  • Female
  • HT29 Cells
  • Humans
  • Hydrogen-Ion Concentration
  • Male
  • Mice, SCID
  • Neoplastic Stem Cells / drug effects*
  • Polyethylene Glycols / chemistry
  • Rats, Sprague-Dawley
  • Xenograft Model Antitumor Assays

Substances

  • Antibiotics, Antineoplastic
  • Aptamers, Nucleotide
  • Drug Carriers
  • EPCAM protein, human
  • Epithelial Cell Adhesion Molecule
  • Polyethylene Glycols
  • Doxorubicin