| Literature DB >> 22472120 |
Johanna Heering1, Nicole Weis, Monika Holeiter, Felix Neugart, Annette Staebler, Tanja N Fehm, Annabell Bischoff, Jürgen Schiller, Stephan Duss, Simone Schmid, Thomas Korte, Andreas Herrmann, Monilola A Olayioye.
Abstract
Triple-negative breast cancers (TNBC) are especially refractory to treatment due to their negative hormone receptor and ErbB2/HER2 status. Therefore, the identification of cancer-associated deregulated signaling pathways is necessary to develop improved targeted therapies. Here, we show that expression of the ceramide transfer protein CERT is reduced in TNBCs. CERT transfers ceramide from the endoplasmic reticulum to the Golgi complex for conversion into sphingomyelin (SM). We provide evidence that by regulating cellular SM levels, CERT determines the signaling output of the EGF receptor (EGFR/ErbB1), which is upregulated in approximately 70% of TNBCs. CERT downregulation in breast cancer cells enhanced ErbB1 lateral mobility, ligand-induced autophosphorylation, internalization, and chemotaxis. Together, our findings provide a link between lipid metabolism at the Golgi with signaling at the plasma membrane, thereby implicating CERT loss in the progression of TNBCs. ©2012 AACREntities:
Mesh:
Substances:
Year: 2012 PMID: 22472120 DOI: 10.1158/0008-5472.CAN-11-3069
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701