Priming BCL-2 to kill: the combination therapy of tamoxifen and ABT-199 in ER+ breast cancer

Breast Cancer Res. 2013;15(5):317. doi: 10.1186/bcr3568.

Abstract

The B-cell lymphoma/leukemia 2 protein (BCL-2) may help many types of cancers to evade cell death. However, identifying exactly where this is the case is a challenge. ABT-199 is a small molecule that selectively inhibits BCL-2, which is currently in clinical trials in lymphoid malignancies. While inhibiting BCL-2 by itself can cause cell death in hematopoietic tumors, single-agent activity is harder to observe in solid tumors. Combining ABT-199 with tamoxifen, the standard endocrine therapy for estrogen receptor-positive breast cancers, 85% of which have BCL-2 expression, represents a new strategy to prime cancer cells for apoptosis and elicit better cancer cell death responses.

Publication types

  • Comment

MeSH terms

  • Animals
  • Breast Neoplasms / drug therapy*
  • Bridged Bicyclo Compounds, Heterocyclic / pharmacology*
  • Female
  • Humans
  • Proto-Oncogene Proteins c-bcl-2 / antagonists & inhibitors*
  • Receptors, Estrogen / analysis*
  • Sulfonamides / pharmacology*

Substances

  • Bridged Bicyclo Compounds, Heterocyclic
  • Proto-Oncogene Proteins c-bcl-2
  • Receptors, Estrogen
  • Sulfonamides