Bcl-xL inhibits p53- but not apoptin-induced apoptosis in head and neck squamous cell carcinoma cell line

Int J Cancer. 2004 Mar;109(1):38-42. doi: 10.1002/ijc.11675.

Abstract

Nonfunctional p53 and especially upregulation of Bcl-x(L) result in advanced disease and poor prognosis of patients suffering head and neck squamous cell carcinoma (HNSCC). Aberrancies of Bcl-x(L) and/or p53 in HNSCC lead to inability of anticancer drugs to induce apoptosis. Bcl-x(L) and/or mutated p53 inhibit the apoptotic process by preventing the mitochondrial release of cytochrome c and/or activation of execution caspases. Here, we report that expression of the avian virus-derived apoptin protein resulted in induction of apoptosis in the HNSCC-derived cell line UMSSC-14B despite the presence of nonfunctional p53. Apoptin activated the execution caspase 3 and induced the release of mitochondrial cytochrome c. Upregulation of Bcl-x(L) in UMSCC-14B cells did not interfere with the apoptin-induced apoptosis, whereas it clearly negatively affected the p53-induced one. Bcl-x(L) significantly decreased the p53-induced cytochrome c release, but not the apoptin-triggered one. Our data demonstrate that apoptin induces apoptosis independent of Bcl-x(L) and p53 and may constitute a potential therapeutic agent for treatment of HNSCC.

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Apoptosis*
  • Blotting, Western
  • Capsid Proteins / metabolism*
  • Carcinoma, Squamous Cell / metabolism*
  • Caspase 3
  • Caspases / metabolism
  • Cell Line, Tumor
  • Cytochromes c / metabolism
  • Fluorescent Antibody Technique, Indirect
  • Genes, p53
  • Head and Neck Neoplasms / metabolism*
  • Humans
  • Microscopy, Fluorescence
  • Mitochondria / metabolism
  • Mutation
  • Plasmids / metabolism
  • Prognosis
  • Proto-Oncogene Proteins c-bcl-2 / biosynthesis*
  • Subcellular Fractions / metabolism
  • Time Factors
  • Transfection
  • Tumor Suppressor Protein p53 / metabolism*
  • Up-Regulation
  • bcl-X Protein

Substances

  • Antineoplastic Agents
  • BCL2L1 protein, human
  • Capsid Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • Tumor Suppressor Protein p53
  • VP3 protein, Chicken anemia virus
  • bcl-X Protein
  • Cytochromes c
  • CASP3 protein, human
  • Caspase 3
  • Caspases