BCL2 and CASP8 regulation by NF-κB differentially affect mitochondrial function and cell fate in antiestrogen-sensitive and -resistant breast cancer cells

Ruchi Nehra, Rebecca B. Riggins, Ayesha N. Shajahan, Alan Zwart, Anatasha C. Crawford, Robert Clarke

Research output: Contribution to journalArticlepeer-review

63 Scopus citations

Abstract

Resistance to endocrine therapies remains a major problem in the management of estrogen receptor-α (ER)-positive breast cancer. We show that inhibition of NF-κB (p65/RELA), either by overexpression of a mutant IκB (IκBSR) or a small-molecule inhibitor of NF-κB (parthenolide; IC50=500 nM in tamoxifen-resistant cells), synergistically restores sensitivity to 4-hydroxytamoxifen (4HT) in resistant MCF7/RR and MCF7/LCC9 cells and further sensitizes MCF-7 and MCF7/LCC1 control cells to 4HT. These effects are independent of changes in either cell cycle distribution or in the level of autophagy measured by inhibition of p62/SQSTM1 expression and cleavage of LC3. NF-κB inhibition restores the ability of 4HT to decrease BCL2 expression, increase mitochondrial membrane permeability, and induce a caspase-dependent apoptotic cell death in resistant cells. Each of these effects is reversed by a caspase 8 (CASP8)-specific inhibitor that blocks enzyme-substrate binding. Thus, increased activation of NF-κB can alter sensitivity to tamoxifen by modulating CASP8 activity, with consequent effects on BCL2 expression, mitochondrial function, and apoptosis. These data provide significant new insights into how molecular signaling affects antiestrogen responsiveness and strongly suggest that a combination of parthenolide and tamoxifen may offer a novel therapeutic approach to the management of some ER-positive breast cancers.

Original languageEnglish (US)
Pages (from-to)2040-2055
Number of pages16
JournalFASEB Journal
Volume24
Issue number6
DOIs
StatePublished - Jun 2010
Externally publishedYes

Keywords

  • Apoptosis
  • Autophagy
  • Breast neoplasms
  • RELA
  • Selective estrogen receptor modulators
  • Tamoxifen

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