Signaling through the antigen receptor of B lymphocytes activates a p53-independent pathway of c-Myc-induced apoptosis

Oncogene. 1999 Jul 15;18(28):4091-8. doi: 10.1038/sj.onc.1202772.

Abstract

Deregulated expression of c-Myc has been shown to induce or enhance apoptosis in various different cell types. c-Myc requires p53 for apoptosis in some but not all the cell types, indicating heterogeneous mechanisms for c-Myc-induced apoptosis. In B lymphoma line WEHI-231, stable expression of c-Myc has been demonstrated to protect cells from BCR-mediated apoptosis. However, stable expression of c-Myc carrying pro-apoptotic functions may generate variant cells resistant to apoptosis. By utilizing an inducible system for c-Myc, we demonstrated here that deregulated expression of c-Myc induced apoptosis of WEHI-231 by itself, indicating that c-Myc induces apoptosis in WEHI-231 as is the case for other cell types. When transactivation of p53 was inactivated, WEHI-231 cells overexpressing c-Myc no longer underwent apoptosis in the absence of other stimuli, but showed markedly enhanced apoptosis in the presence of BCR ligation. These results indicate that deregulated c-Myc expression enhances apoptosis by a p53-independent pathway in the presence of BCR signaling but requires p53 for apoptosis in the absence of BCR crosslinking in WEHI-231. BCR ligation may thus activate a p53-independent pathway of c-Myc-induced apoptosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / physiology*
  • B-Lymphocytes / cytology*
  • B-Lymphocytes / drug effects
  • Estradiol / pharmacology
  • Gene Expression Regulation, Neoplastic*
  • Genes, myc
  • Genes, p53
  • Humans
  • Lymphocyte Activation*
  • Lymphoma, B-Cell / pathology
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / physiology
  • Proto-Oncogene Proteins c-myc / physiology*
  • Receptors, Antigen, B-Cell / physiology*
  • Recombinant Fusion Proteins / physiology
  • Signal Transduction*
  • Transcriptional Activation
  • Transfection
  • Tumor Cells, Cultured / drug effects
  • Tumor Suppressor Protein p53 / physiology*

Substances

  • Neoplasm Proteins
  • Proto-Oncogene Proteins c-myc
  • Receptors, Antigen, B-Cell
  • Recombinant Fusion Proteins
  • Tumor Suppressor Protein p53
  • Estradiol