CD151 regulates expression of FGFR2 in breast cancer cells via PKC-dependent pathways

Author:

Sadej Rafal1,Lu Xiaohong2,Turczyk Lukasz1,Novitskaya Vera2,Lopez-Clavijo Andrea F.3,Kordek Radzisław4,Potemski Piotr4,Wakelam Michael J. O.3,Romanska Hanna4,Berditchevski Fedor2ORCID

Affiliation:

1. Department of Molecular Enzymology and University of Gdansk and Medical University of Gdansk, Gdansk, Poland

2. Institute of Cancer and Genomic Sciences, The University of Birmingham, Edgbaston, Birmingham, UK

3. Babraham Institute, Cambridge, UK

4. Department of Pathology and Chemotherapy, Medical University of Łόdź, Poland

Abstract

Expression of the tetraspanin CD151 is frequently upregulated in epithelial malignancies and correlates with poor prognosis. Here we report that CD151 is involved in regulation of the expression of fibroblast growth factor receptor 2 (FGFR2). Depletion of CD151 in breast cancer cells resulted in an increased level of FGFR2. Accordingly, an inverse correlation between CD151 and FGFR2 was observed in breast cancer tissues. CD151-dependent regulation of the FGFR2 expression relies on post-transcriptional mechanisms involving HuR/ELAVL1, a multifunctional RNA binding protein, and the assembly of processing bodies (P-bodies). Depletion of CD151 correlated with inhibition of PKC, a well-established downstream target of CD151. Accordingly, the levels of dialcylglycerol species were decreased in CD151-negative cells, and inhibition of PKC resulted in the increased expression of FGFR2. Whilst expression of FGFR2 itself did not correlate with any of the clinicopathological data, the FGFR2-/CD151+ patients are more likely to develop lymph node metastasis. Conversely, FGFR2-/CD151- patients demonstrated better overall survival. These results illustrate functional interdependency between CD151 complexes and FGFR2 and suggest a previously unsuspected role of CD151 in breast tumourigenesis.

Funder

Breast Cancer Campaign

Publisher

The Company of Biologists

Subject

Cell Biology

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