Expression of Notch-1 and its ligands, Delta-like-1 and Jagged-1, is critical for glioma cell survival and proliferation

Cancer Res. 2005 Mar 15;65(6):2353-63. doi: 10.1158/0008-5472.CAN-04-1890.

Abstract

The Notch family of proteins plays an integral role in determining cell fates, such as proliferation, differentiation, and apoptosis. We show that Notch-1 and its ligands, Delta-like-1 and Jagged-1, are overexpressed in many glioma cell lines and primary human gliomas. Immunohistochemistry of a primary human glioma tissue array shows the presence in the nucleus of the Notch-1 intracellular domain, indicating Notch-1 activation in situ. Down-regulation of Notch-1, Delta-like-1, or Jagged-1 by RNA interference induces apoptosis and inhibits proliferation in multiple glioma cell lines. In addition, pretreatment of glioma cells with Notch-1 or Delta-like-1 small interfering RNA significantly prolongs survival in a murine orthotopic brain tumor model. These results show, for the first time, the dependence of cancer cells on a single Notch ligand; they also suggest a potential Notch juxtacrine/autocrine loop in gliomas. Notch-1 and its ligands may present novel therapeutic targets in the treatment of glioma.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Brain Neoplasms / genetics
  • Brain Neoplasms / metabolism*
  • Brain Neoplasms / pathology*
  • Calcium-Binding Proteins
  • Cell Growth Processes / physiology
  • Cell Line, Tumor
  • Cell Survival / physiology
  • Down-Regulation
  • Gene Expression Regulation, Neoplastic
  • Glioma / genetics
  • Glioma / metabolism*
  • Glioma / pathology*
  • Glycoproteins / biosynthesis*
  • Glycoproteins / genetics
  • Humans
  • Intercellular Signaling Peptides and Proteins
  • Jagged-1 Protein
  • Ligands
  • Membrane Proteins / biosynthesis*
  • Membrane Proteins / genetics
  • Mice
  • Neoplasm Transplantation
  • RNA Interference
  • RNA, Small Interfering / genetics
  • Receptor, Notch1
  • Receptors, Cell Surface / biosynthesis*
  • Receptors, Cell Surface / genetics
  • Serrate-Jagged Proteins
  • Transcription Factors / biosynthesis*
  • Transcription Factors / genetics
  • Transplantation, Heterologous

Substances

  • Calcium-Binding Proteins
  • Glycoproteins
  • Intercellular Signaling Peptides and Proteins
  • JAG1 protein, human
  • Jag1 protein, mouse
  • Jagged-1 Protein
  • Ligands
  • Membrane Proteins
  • NOTCH1 protein, human
  • Notch1 protein, mouse
  • RNA, Small Interfering
  • Receptor, Notch1
  • Receptors, Cell Surface
  • Serrate-Jagged Proteins
  • Transcription Factors