Fetal human neural progenitors can be the target for tumor transformation

Neuroreport. 2004 Aug 26;15(12):1907-12. doi: 10.1097/00001756-200408260-00015.

Abstract

The hypothesis that stem cells may seed cancer has emerged from the cancer stem cells concept. However, the experimental systems necessary to provide more direct evidence to support the hypothesis have been lacking. We have used fetal neural progenitor cells (hNPC) transduced with the telomerase hTERT gene to investigate the neoplastic potential of hNPCs. The hTERT-transduced line, hNPCs-G3 lost normal diploid karyotype, showed loss of contact inhibition, anchorage independence, and formed neuroblastoma-like tumours in all of 10 mice. These data suggest that hNPCs have the potential for neoplastic transformation. These data have implications for providing a novel tool to test the feasibility of new anticancer treatment strategies and raise the possibility of a risk for the use of hNPCs in cell transplantation.

Publication types

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

MeSH terms

  • Animals
  • Blotting, Southern
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism
  • Cell Count / methods
  • Cell Differentiation / physiology
  • Cell Line, Tumor
  • Cell Transformation, Neoplastic*
  • DNA / metabolism
  • Fetus / cytology*
  • GTP-Binding Proteins
  • Gene Expression Regulation, Neoplastic / physiology*
  • Glial Fibrillary Acidic Protein / genetics
  • Glial Fibrillary Acidic Protein / metabolism
  • Humans
  • Immunohistochemistry / methods
  • Intermediate Filament Proteins / genetics
  • Karyotyping / methods
  • Mice
  • Mice, Nude / metabolism
  • Microtubule-Associated Proteins / genetics
  • Microtubule-Associated Proteins / metabolism
  • Nerve Tissue Proteins / genetics
  • Nestin
  • Neurons / physiology*
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism
  • Polycomb Repressive Complex 1
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / metabolism
  • RNA, Messenger / biosynthesis
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction / methods
  • Staining and Labeling
  • Stem Cells / physiology*
  • Telomere / metabolism
  • Time Factors
  • Transduction, Genetic / methods
  • Tubulin / genetics
  • Tubulin / metabolism

Substances

  • BMI1 protein, human
  • Carrier Proteins
  • GNL3 protein, human
  • Glial Fibrillary Acidic Protein
  • Intermediate Filament Proteins
  • Microtubule-Associated Proteins
  • NES protein, human
  • Nerve Tissue Proteins
  • Nes protein, mouse
  • Nestin
  • Nuclear Proteins
  • Proto-Oncogene Proteins
  • RNA, Messenger
  • Repressor Proteins
  • Tubulin
  • DNA
  • Polycomb Repressive Complex 1
  • GTP-Binding Proteins