Expression of anti-apoptosis genes determines the response of adrenal cancer to apoptosis-inducing chemotherapy

Anticancer Res. 2010 Dec;30(12):4805-9.

Abstract

Background: This study tested the hypothesis that response of adrenal cortical carcinoma (ACC) to pro-apoptosis drugs depends on expression of anti-apoptosis genes.

Materials and methods: Expression of Bcl-2 and Bcl-XL proteins was determined in two human adrenal cancer cell lines, NCI-H-295 and RL-251. Two pro-apoptosis drugs, gossypol (G) and docetaxel (D) were tested in vitro and in vivo in a human ACC/SCID mouse chimera.

Results: Bcl-XL was strongly expressed in RL-251 but not in H-295 and neither expressed the Bcl-2 protein. G and D induced greater dose-dependent inhibition of cell proliferation in RL-251 than in H-295 cells and completely suppressed growth of tumors with high expression of Bcl-XL (p<0.05) while there was no growth suppression in tumors without Bcl-XL expression.

Conclusion: This study provided proof of concept that expression of Bcl-XL determines response to pro-apoptosis drugs. Profiling adrenal tumors for expression of anti-apoptosis genes may provide clues to their potential response to drugs that induce apoptosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenal Cortex Neoplasms / drug therapy*
  • Adrenal Cortex Neoplasms / genetics*
  • Adrenal Cortex Neoplasms / metabolism
  • Adrenal Cortex Neoplasms / pathology
  • Animals
  • Apoptosis / drug effects*
  • Apoptosis / genetics*
  • Cell Line, Tumor
  • Docetaxel
  • Genes, bcl-2
  • Gossypol / pharmacology
  • Humans
  • Mice
  • Mice, SCID
  • Proto-Oncogene Proteins c-bcl-2 / biosynthesis*
  • Proto-Oncogene Proteins c-bcl-2 / genetics
  • Taxoids / pharmacology
  • bcl-X Protein / biosynthesis*
  • bcl-X Protein / genetics

Substances

  • BCL2L1 protein, human
  • Proto-Oncogene Proteins c-bcl-2
  • Taxoids
  • bcl-X Protein
  • Docetaxel
  • Gossypol