Gene expression profiling of tumor-initiating stem cells from mouse Krebs-2 carcinoma using a novel marker of poorly differentiated cells

Oncotarget. 2017 Feb 7;8(6):9425-9441. doi: 10.18632/oncotarget.14116.

Abstract

Using the ability of poorly differentiated cells to natively internalize fragments of extracellular double-stranded DNA as a marker, we isolated a tumorigenic subpopulation present in Krebs-2 ascites that demonstrated the features of tumor-inducing cancer stem cells. Having combined TAMRA-labeled DNA probe and the power of RNA-seq technology, we identified a set of 168 genes specifically expressed in TAMRA-positive cells (tumor-initiating stem cells), these genes remaining silent in TAMRA-negative cancer cells. TAMRA+ cells displayed gene expression signatures characteristic of both stem cells and cancer cells. The observed expression differences between TAMRA+ and TAMRA- cells were validated by Real Time PCR. The results obtained corroborated the biological data that TAMRA+ murine Krebs-2 tumor cells are tumor-initiating stem cells. The approach developed can be applied to profile any poorly differentiated cell types that are capable of immanent internalization of double-stranded DNA.

Keywords: DNA internalization; RNAseq; Real Time PCR; TAMRA; tumor-initiating stem cells.

MeSH terms

  • Alu Elements
  • Animals
  • Biomarkers, Tumor / genetics*
  • Biomarkers, Tumor / metabolism
  • Carcinoma, Krebs 2 / genetics*
  • Carcinoma, Krebs 2 / pathology
  • Cell Differentiation*
  • DNA / genetics
  • DNA / metabolism
  • Fluorescent Dyes / metabolism
  • Gene Expression Profiling / methods*
  • Gene Expression Regulation, Neoplastic
  • Gene Regulatory Networks
  • High-Throughput Nucleotide Sequencing
  • Neoplastic Stem Cells / metabolism
  • Neoplastic Stem Cells / pathology
  • Phenotype
  • Real-Time Polymerase Chain Reaction
  • Rhodamines / metabolism
  • Sequence Analysis, RNA
  • Signal Transduction
  • Transcriptome*

Substances

  • 5-carboxytetramethylrhodamine succinimidyl ester
  • Biomarkers, Tumor
  • Fluorescent Dyes
  • Rhodamines
  • DNA