SWI/SNF chromatin remodeling enzyme ATPases promote cell proliferation in normal mammary epithelial cells

J Cell Physiol. 2010 Jun;223(3):667-78. doi: 10.1002/jcp.22072.

Abstract

The ATPase subunits of the SWI/SNF chromatin remodeling enzymes, Brahma (BRM) and Brahma-related gene 1 (BRG1), can induce cell cycle arrest in BRM and BRG1 deficient tumor cell lines, and mice heterozygous for Brg1 are pre-disposed to breast tumors, implicating loss of BRG1 as a mechanism for unregulated cell proliferation. To test the hypothesis that loss of BRG1 can contribute to breast cancer, we utilized RNA interference to reduce the amounts of BRM or BRG1 protein in the nonmalignant mammary epithelial cell line, MCF-10A. When grown in reconstituted basement membrane (rBM), these cells develop into acini that resemble the lobes of normal breast tissue. Contrary to expectations, knockdown of either BRM or BRG1 resulted in an inhibition of cell proliferation in monolayer cultures. This inhibition was strikingly enhanced in three-dimensional rBM culture, although some BRM-depleted cells were later able to resume proliferation. Cells did not arrest in any specific stage of the cell cycle; instead, the cell cycle length increased by approximately 50%. Thus, SWI/SNF ATPases promote cell cycle progression in nonmalignant mammary epithelial cells.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adenosine Triphosphatases / metabolism*
  • Basement Membrane / drug effects
  • Basement Membrane / metabolism
  • Cell Cycle / drug effects
  • Cell Line
  • Cell Proliferation / drug effects
  • Chromatin Assembly and Disassembly* / drug effects
  • DNA Helicases / deficiency
  • DNA Helicases / metabolism*
  • Doxycycline / pharmacology
  • Epithelial Cells / cytology*
  • Epithelial Cells / enzymology*
  • Female
  • Gene Knockdown Techniques
  • Humans
  • Mammary Glands, Human / cytology*
  • Nuclear Proteins / deficiency
  • Nuclear Proteins / metabolism*
  • Protein Subunits / metabolism
  • RNA, Small Interfering / metabolism
  • RNA, Small Nucleolar / genetics
  • RNA, Small Nucleolar / metabolism
  • Transcription Factors / deficiency
  • Transcription Factors / metabolism*
  • Up-Regulation / drug effects

Substances

  • Nuclear Proteins
  • Protein Subunits
  • RNA, Small Interfering
  • RNA, Small Nucleolar
  • SMARCA2 protein, human
  • Transcription Factors
  • growth arrest specific transcript 5
  • Adenosine Triphosphatases
  • SMARCA4 protein, human
  • DNA Helicases
  • Doxycycline