Survivin enhances Fas ligand expression via up-regulation of specificity protein 1-mediated gene transcription in colon cancer cells

J Immunol. 2004 Mar 15;172(6):3922-9. doi: 10.4049/jimmunol.172.6.3922.

Abstract

Cancer cells are thought to possess mechanisms for evading the host's immune surveillance system. Survivin, a member of the inhibitor-of-apoptosis family overexpressed by cancer cells, inhibits Fas-mediated apoptosis induced by immune cells. In addition, cancer cells express Fas ligand (FasL) on their surfaces as a counterattack against immune cells. Mechanisms by which cancer cells express FasL, including involvement of survivin, are unclear. In the present study, we demonstrated that survivin up-regulated FasL expression and investigated how this might occur. Quantitative immunostaining showed correlation between survivin and FasL protein expression in colon cancer tissues (r=0.79). FasL expression was up-regulated in LS180 colon cancer cells transfected with the survivin gene. Transfectants showed increased cytotoxicity against a Fas-sensitive human T leukemia cell line, Jurkat. In contrast, FasL expression was down-regulated in SW480 cells transfected with a small inhibitory RNA to prevent survivin expression. Survivin gene transfectants showed increased DNA binding of transcription factor specificity protein 1 (Sp1) to the FasL promoter, and up-regulation of Sp1 phosphorylation at serine and threonine residues; the total amount of Sp1 was unchanged. Thus, survivin enables cancer cells not only to suppress immune cell attack by inhibiting Fas-mediated apoptotic signaling, but to attack immune cells by induction of FasL.

MeSH terms

  • Adjuvants, Immunologic / biosynthesis
  • Adjuvants, Immunologic / genetics
  • Adjuvants, Immunologic / physiology*
  • Cell Line, Tumor
  • Colonic Neoplasms / genetics*
  • Colonic Neoplasms / immunology*
  • Colonic Neoplasms / metabolism
  • Down-Regulation / immunology
  • Fas Ligand Protein
  • Humans
  • Inhibitor of Apoptosis Proteins
  • Jurkat Cells
  • Ligands
  • Membrane Glycoproteins / antagonists & inhibitors
  • Membrane Glycoproteins / biosynthesis*
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / metabolism
  • Microtubule-Associated Proteins / antagonists & inhibitors
  • Microtubule-Associated Proteins / biosynthesis
  • Microtubule-Associated Proteins / genetics
  • Microtubule-Associated Proteins / physiology*
  • Neoplasm Proteins
  • Phosphorylation
  • Promoter Regions, Genetic / immunology
  • Sp1 Transcription Factor / metabolism
  • Sp1 Transcription Factor / physiology*
  • Survivin
  • Transcription, Genetic / immunology
  • Transfection
  • Up-Regulation / immunology*
  • fas Receptor / metabolism

Substances

  • Adjuvants, Immunologic
  • BIRC5 protein, human
  • FASLG protein, human
  • Fas Ligand Protein
  • Inhibitor of Apoptosis Proteins
  • Ligands
  • Membrane Glycoproteins
  • Microtubule-Associated Proteins
  • Neoplasm Proteins
  • Sp1 Transcription Factor
  • Survivin
  • fas Receptor