Interferon-gamma-induced sensitization of colon carcinomas to ZD9331 targets caspases, downstream of Fas, independent of mitochondrial signaling and the inhibitor of apoptosis survivin

Clin Cancer Res. 2003 Dec 15;9(17):6504-15.

Abstract

We have demonstrated previously a Fas-dependent component in thymineless death of human colon carcinoma cells. Importantly, the cytotoxic effects of thymidine deprivation induced by 5-fluorouracil (FUra) combined with leucovorin (LV) was enhanced by IFN-gamma, and the synergism was shown to be dependent on Fas, FUra-induced DNA damage, and independent of p53. Subsequently we examined the potential for synergistic interactions between IFN-gamma and the specific thymidylate synthase inhibitor, ZD9331. IFN-gamma sensitized colon carcinomas to ZD9331-induced apoptosis and loss in clonogenic survival, also dependent on ZD9331-induced DNA damage, independent of p53. Synergism occurred in HCT116, demonstrating previously RNA-mediated FUra/LV cytotoxicity that could not be potentiated by IFN-gamma. Manipulation of the Fas death receptor pathway from the level of the receptor (Nok1/Nok2, Fas overexpression, and DN-FADD) to the mitochondria (Bcl-xL and Bcl-2) did not modulate ZD9331 +/- IFN-gamma-induced cytotoxicity in HT29, with the exception that Nok1/Nok2-blocking antibodies partially protected HT29 from the cytotoxic activity of ZD9331 alone. However, IFN-gamma alone (but not ZD9331) up-regulated the expression of caspases -3, -4, -7, and -8, and in combination with ZD9331 demonstrated enhanced caspase activation and cleavage of poly(ADP-ribose) polymerase that was not prevented by overexpression of Bcl-2. Additionally, IFN-gamma increased the activity of the proteasome in HT29, leading to selective down-regulation of the antiapoptotic protein survivin, whereas simultaneously increasing Fas expression. However, reduction in the survivin:Fas ratio by transfection of survivin small interfering RNA and/or overexpression of Fas did not affect sensitivity of HT29 to ZD9331 +/- IFN-gamma. Data demonstrate that IFN-gamma combined with ZD9331 is synergistic in additional cell lines that demonstrate RNA-mediated FUra/LV cytotoxicity, and that a major target of interaction is at the level of caspases, downstream of Fas, and independent of involvement of either the mitochondria or survivin.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Apoptosis
  • Caspase 3
  • Caspase 7
  • Caspase 8
  • Caspases / biosynthesis
  • Caspases / metabolism*
  • Caspases, Initiator
  • Cell Line
  • Cell Line, Tumor
  • Colonic Neoplasms / drug therapy*
  • Cysteine Endopeptidases / metabolism
  • DNA, Complementary / metabolism
  • Dose-Response Relationship, Drug
  • Down-Regulation
  • Enzyme Inhibitors / pharmacology
  • Fluorouracil / metabolism
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Immunoblotting
  • Inhibitor of Apoptosis Proteins
  • Interferon-gamma / metabolism*
  • Kinetics
  • Microtubule-Associated Proteins / metabolism*
  • Mitochondria / metabolism*
  • Multienzyme Complexes / metabolism
  • Neoplasm Proteins
  • Oligonucleotide Array Sequence Analysis
  • Proteasome Endopeptidase Complex
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Quinazolines / therapeutic use*
  • RNA, Small Interfering / metabolism
  • Retroviridae / genetics
  • Signal Transduction
  • Survivin
  • Time Factors
  • Transfection
  • Tumor Suppressor Protein p53 / metabolism
  • Up-Regulation
  • bcl-X Protein
  • fas Receptor / metabolism*

Substances

  • Antineoplastic Agents
  • BCL2L1 protein, human
  • BIRC5 protein, human
  • DNA, Complementary
  • Enzyme Inhibitors
  • Inhibitor of Apoptosis Proteins
  • Microtubule-Associated Proteins
  • Multienzyme Complexes
  • Neoplasm Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • Quinazolines
  • RNA, Small Interfering
  • Survivin
  • Tumor Suppressor Protein p53
  • ZD 9331
  • bcl-X Protein
  • fas Receptor
  • Interferon-gamma
  • CASP3 protein, human
  • CASP4 protein, human
  • CASP7 protein, human
  • CASP8 protein, human
  • Caspase 3
  • Caspase 7
  • Caspase 8
  • Caspases
  • Caspases, Initiator
  • Cysteine Endopeptidases
  • Proteasome Endopeptidase Complex
  • Fluorouracil