Pro-apoptotic Bim suppresses breast tumor cell metastasis and is a target gene of SNAI2

D. Merino, S. A. Best, M. L. Asselin-Labat, F. Vaillant, B. Pal, R. A. Dickins, R. L. Anderson, A. Strasser, P. Bouillet, G. J. Lindeman, J. E. Visvader

Research output: Contribution to journalArticlepeer-review

27 Scopus citations


Evasion of cell death is fundamental to the development of cancer and its metastasis. The role of the BCL-2-mediated (intrinsic) apoptotic program in these processes remains poorly understood. Here we have investigated the relevance of the pro-apoptotic protein BIM to breast cancer progression using the MMTV-Polyoma middle-T (PyMT) transgenic model. BIM deficiency in PyMT females did not affect primary tumor growth, but substantially increased the survival of metastatic cells within the lung. These data reveal a role for BIM in the suppression of breast cancer metastasis. Intriguingly, we observed a striking correlation between the expression of BIM and the epithelial to mesenchymal transition transcription factor SNAI2 at the proliferative edge of the tumors. Overexpression and knockdown studies confirmed that these two genes were coordinately expressed, and chromatin immunoprecipitation analysis further revealed that Bim is a target of SNAI2. Taken together, our findings suggest that SNAI2-driven BIM-induced apoptosis may temper metastasis by governing the survival of disseminating breast tumor cells.

Original languageEnglish (US)
Pages (from-to)3926-3934
Number of pages9
Issue number30
StatePublished - Jul 23 2015

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Cancer Research


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