MiR-106b~25 cluster regulates multidrug resistance in an ABC transporter-independent manner via downregulation of EP300

Oncol Rep. 2016 Feb;35(2):1170-8. doi: 10.3892/or.2015.4412. Epub 2015 Nov 12.

Abstract

MicroRNA (miR)-106b~25 cluster regulates bypass of doxorubicin and γ-radiation induced senescence by downregulation of the E-cadherin transcriptional activator EP300. We asked whether upregulation of miR-106~25 cluster generates cells with a truly multidrug resistant (MDR) phenotype and whether this is due to upregulation of the ATP-binding cassette (ABC) transporter P-glycoprotein. We used minimally transformed mammary epithelial breast cancer cells (MTMECs) in which the miR-106b~25 cluster was experimentally upregulated by lentiviral transfection or in which hairpins targeting either EP300 or E-cadherin mRNAs have been expressed with lentiviruses. We find that overexpression of miR-106b~25 cluster led to the generation of MDR MTMECs (resistant to etoposide, colchicine and paclitaxel). Paclitaxel resistance was also studied after experimental downregulation of EP300 or E-cadherin. However none of these cells overexpressed P-glycoprotein or where able to efflux a fluorescent derivative of paclitaxel, making this phenotype drug-transporter independent. Paclitaxel treatment in MTMECs led to an increase in early apoptotic cells (Annexin V-positive), activation of caspase-9 and increase in the proportion of cells at the G2/M phase of the cell cycle. However, MTMEC overexpressing miR-106b~25 cluster, or with EP300 or E-cadherin downregulated, showed less activation of apoptosis, caspase-9 and caspase-3/-7 activities. Thus, miR-106b~25 cluster controls transporter-independent MDR by apoptosis evasion via downregulation of EP300.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP-Binding Cassette Transporters
  • Antineoplastic Agents / pharmacology*
  • Apoptosis
  • Breast / cytology*
  • Cadherins / biosynthesis
  • Cadherins / genetics
  • Cell Line, Transformed
  • Colchicine / pharmacology
  • Down-Regulation
  • Doxorubicin / pharmacology
  • Drug Resistance, Multiple / genetics*
  • Drug Resistance, Neoplasm / genetics*
  • E1A-Associated p300 Protein / biosynthesis*
  • E1A-Associated p300 Protein / genetics
  • Epithelial Cells / drug effects*
  • Epithelial Cells / radiation effects
  • Etoposide / pharmacology
  • Gamma Rays
  • Humans
  • MicroRNAs / genetics*
  • Multigene Family
  • Neoplasm Proteins / genetics*
  • Neoplasm Proteins / physiology
  • Paclitaxel / pharmacology
  • Phenotype
  • RNA, Neoplasm / genetics*
  • Transduction, Genetic
  • Tumor Stem Cell Assay

Substances

  • ATP-Binding Cassette Transporters
  • Antineoplastic Agents
  • Cadherins
  • MIRN106 microRNA, human
  • MicroRNAs
  • Neoplasm Proteins
  • RNA, Neoplasm
  • Etoposide
  • Doxorubicin
  • E1A-Associated p300 Protein
  • EP300 protein, human
  • Paclitaxel
  • Colchicine