Herpes simplex virus thymidine kinase/ganciclovir-induced apoptosis involves ligand-independent death receptor aggregation and activation of caspases

Proc Natl Acad Sci U S A. 1999 Jul 20;96(15):8699-704. doi: 10.1073/pnas.96.15.8699.

Abstract

Suicide gene therapy systems such as the herpes simplex thymidine kinase/ganciclovir system (TK/GCV) may kill cancer cells by apoptosis through as yet undefined mechanisms. Here we show that TK/GCV treatment induces p53 accumulation and increases cell surface expression of CD95 and tumor necrosis factor receptor, which is likely to involve p53-mediated translocation of CD95 to the cell surface. TK/GCV-induced apoptosis involves CD95-L-independent CD95 aggregation leading to the formation of a Fas-associated death domain protein (FADD) and caspase-8-containing, death-inducing signaling complex. Dominant negative FADD, the caspase-8 inhibitor zIETD-fmk [Z-Ile-Glu(OMe)-Thr-Asp(OMe)-fluoromethylketone], and zVAD-fmk (Z-Val-Ala-Asp-fluoromethylketone) partially abrogate TK/GCV-induced apoptosis. In addition to apoptosis induction, TK/GCV treatment strongly sensitizes for CD95-L-, TNF-, and TNF-related, apoptosis-inducing, ligand (TRAIL)-induced cell death in constitutively resistant cells. These findings may be used to increase the efficacy of TK/GCV and other suicide gene therapy systems for the treatment of cancer.

MeSH terms

  • Adaptor Proteins, Signal Transducing*
  • Antiviral Agents / pharmacology
  • Apoptosis / drug effects*
  • Apoptosis Regulatory Proteins
  • Brefeldin A / pharmacology
  • Carrier Proteins / metabolism
  • Caspases / metabolism*
  • Enzyme Activation
  • Fas Ligand Protein
  • Fas-Associated Death Domain Protein
  • Ganciclovir / pharmacology
  • Genetic Therapy / methods
  • Humans
  • Membrane Glycoproteins / metabolism
  • Protease Inhibitors / pharmacology
  • Receptors, Tumor Necrosis Factor / metabolism*
  • Simplexvirus / enzymology*
  • TNF-Related Apoptosis-Inducing Ligand
  • Thymidine Kinase / metabolism*
  • Transfection
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / metabolism
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • Adaptor Proteins, Signal Transducing
  • Antiviral Agents
  • Apoptosis Regulatory Proteins
  • Carrier Proteins
  • FADD protein, human
  • FASLG protein, human
  • Fas Ligand Protein
  • Fas-Associated Death Domain Protein
  • Membrane Glycoproteins
  • Protease Inhibitors
  • Receptors, Tumor Necrosis Factor
  • TNF-Related Apoptosis-Inducing Ligand
  • TNFSF10 protein, human
  • Tumor Necrosis Factor-alpha
  • Tumor Suppressor Protein p53
  • Brefeldin A
  • Thymidine Kinase
  • Caspases
  • Ganciclovir