Role of TGF-β receptor III localization in polarity and breast cancer progression.

Journal Article (Journal Article)

The majority of breast cancers originate from the highly polarized luminal epithelial cells lining the breast ducts. However, cell polarity is often lost during breast cancer progression. The type III transforming growth factor-β cell surface receptor (TβRIII) functions as a suppressor of breast cancer progression and also regulates the process of epithelial-to-mesenchymal transition (EMT), a consequence of which is the loss of cell polarity. Many cell surface proteins exhibit polarized expression, being targeted specifically to the apical or basolateral domains. Here we demonstrate that TβRIII is basolaterally localized in polarized breast epithelial cells and that disruption of the basolateral targeting of TβRIII through a single amino acid mutation of proline 826 in the cytosolic domain results in global loss of cell polarity through enhanced EMT. In addition, the mistargeting of TβRIII results in enhanced proliferation, migration, and invasion in vitro and enhanced tumor formation and invasion in an in vivo mouse model of breast carcinoma. These results suggest that proper localization of TβRIII is critical for maintenance of epithelial cell polarity and phenotype and expand the mechanisms by which TβRIII prevents breast cancer initiation and progression.

Full Text

Duke Authors

Cited Authors

  • Meyer, AE; Gatza, CE; How, T; Starr, M; Nixon, AB; Blobe, GC

Published Date

  • August 1, 2014

Published In

Volume / Issue

  • 25 / 15

Start / End Page

  • 2291 - 2304

PubMed ID

  • 24870032

Pubmed Central ID

  • PMC4116303

Electronic International Standard Serial Number (EISSN)

  • 1939-4586

Digital Object Identifier (DOI)

  • 10.1091/mbc.E14-03-0825


  • eng

Conference Location

  • United States