Journal Article

The PDGFRβ/ERK1/2 pathway regulates CDCP1 expression in triple-negative breast cancer

Sozzi, Gabriella, Forte, Luca, Ghirelli, Cristina, Belmonte, Beatrice, Iorio, Marilena Valeria, Turdo, Federica, Campiglio, Manuela, Casalini, Patrizia, Gasparini, Patrizia, D’Ippolito, Elvira, Aiello, Piera, Bianchi, Francesca, Agresti, Roberto, Sfondrini, Lucia, Tagliabue, Elda

2018

Overview

Background CDCP1, a transmembrane protein with tumor pro-metastatic activity, was recently identified as a prognostic marker in TNBC, the most aggressive breast cancer subtype still lacking an effective molecular targeted therapy. The mechanisms driving CDCP1 over-expression are not fully understood, although several stimuli derived from tumor microenvironment, such as factors present in Wound Healing Fluids (WHFs), reportedly increase CDCP1 levels. Methods The expression of CDCP1, PDGFRβ and ERK1/2cell was tested by Western blot after stimulation of MDA-MB-231 cells with PDGF-BB and, similarly, in presence or not of ERK1/2 inhibitor in a panel of TNBC cell lines. Knock-down of PDGFRβ was established in MDA-MB-231 cells to detect CDCP1 upon WHF treatment. Immunohistochemical staining was used to detect the expression of CDCP1 and PDGFRβ in TNBC clinical samples. Results We discovered that PDGF-BB-mediated activation of PDGFRβ increases CDCP1 protein expression through the downstream activation of ERK1/2. Inhibition of ERK1/2 activity reduced per se CDCP1 expression, evidence strengthening its role in CDCP1 expression regulation. Knock-down of PDGFRβ in TNBC cells impaired CDCP1 increase induced by WHF treatment, highlighting the role if this receptor as a central player of the WHF-mediated CDCP1 induction. A significant association between CDCP1 and PDGFRβ immunohistochemical staining was observed in TNBC specimens, independently of CDCP1 gene gain, thus corroborating the relevance of the PDGF-BB/PDGFRβ axis in the modulation of CDCP1 expression. Conclusion We have identified PDGF-BB/PDGFRβ–mediated pathway as a novel player in the regulation of CDCP1 in TNCBs through ERK1/2 activation. Our results provide the basis for the potential use of PDGFRβ and ERK1/2 inhibitors in targeting the aggressive features of CDCP1-positive TNBCs.

• Publisher: BioMed Central,Springer Nature B.V,BMC
• Subject: Antigens, CD - metabolism / Becaplermin - pharmacology / Biomedical and Life Sciences / Biomedicine / Breast cancer / Cancer Research / Cancer therapies / CDCP1 / Cell adhesion & migration / Cell Adhesion Molecules - metabolism / Cell Line, Tumor / Epidermal growth factor / ERK1/2 / Extracellular signal-regulated kinase / Female / FISH / Gene Expression Regulation, Neoplastic / Gene Knockdown Techniques / Health Promotion and Disease Prevention / Humans / Kinases / MAP Kinase Signaling System - drug effects / MAP Kinase Signaling System - genetics / Medicine/Public Health / Metastases / Middle Aged / Mitogen-Activated Protein Kinase 1 - antagonists & inhibitors / Mitogen-Activated Protein Kinase 1 - metabolism / Mitogen-Activated Protein Kinase 3 - antagonists & inhibitors / Mitogen-Activated Protein Kinase 3 - metabolism / Neoplasm Proteins - metabolism / Oncology / Overexpression / PDGF-BB / PDGFRβ / Platelet-derived growth factor / Platelet-derived growth factor BB / Protein expression / Proteins / Receptor, Platelet-Derived Growth Factor beta - genetics / Receptor, Platelet-Derived Growth Factor beta - metabolism / Research Article / RNA, Small Interfering - metabolism / Surgical Oncology / TNBC / Translational oncology / Triple Negative Breast Neoplasms - genetics / Triple Negative Breast Neoplasms - pathology / Tumors / Up-Regulation / Wound healing