Crosstalk between CXCR4/ACKR3 and EGFR signaling in breast cancer cells
Entidad
UAM. Departamento de Biología MolecularEditor
MDPIFecha de edición
2022-10-01Cita
10.3390/ijms231911887
International Journal of Molecular Sciences 23.19 (2022): 11887
ISSN
1661-6596 (print); 1422-0067 (online)DOI
10.3390/ijms231911887Proyecto
info:eu-repo/grantAgreement/EC/H2020/860229/EU//ONCORNET2.0; Gobierno de España. PID2020-117218RB-I00; Comunidad de Madrid. S2017/BMD-3671/INFLAMUNE-CMVersión del editor
https://doi.org/10.3390/ijms231911887Materias
Chemokine Receptor CXCR4; Chemokine Receptor CXCR7; G Protein Coupled Receptor Kinase 2; Mitogen Activated Protein Kinase 1; Stromal Cell Derived Factor 1; Biología y Biomedicina / BiologíaDerechos
© 2022 by the authorsResumen
A better understanding of the complex crosstalk among key receptors and signaling pathways involved in cancer progression is needed to improve current therapies. We have investigated in cell models representative of the major subtypes of breast cancer (BC) the interplay between the chemokine CXCL12/CXCR4/ACKR3 and EGF receptor (EGFR) family signaling cascades. These cell lines display a high heterogeneity in expression profiles of CXCR4/ACKR3 chemokine receptors, with a predominant intracellular localization and different proportions of cell surface CXCR4+, ACKR3+ or double-positive cell subpopulations, and display an overall modest activation of oncogenic pathways in response to exogenous CXCL12 alone. Interestingly, we find that in MDA-MB-361 (luminal B subtype, Her2-overexpressing), but not in MCF7 (luminal A) or MDA-MB-231 (triple negative) cells, CXCR4/ACKR3 and EGFR receptor families share signaling components and crosstalk mechanisms to concurrently promote ERK1/2 activation, with a key involvement of the G protein-coupled receptor kinase 2 (GRK2) signaling hub and the cytosolic tyrosine kinase Src. Our findings suggest that in certain BC subtypes, a relevant cooperation between CXCR4/ACKR3 and growth factor receptors takes place to integrate concurrent signals emanating from the tumor microenvironment and foster cancer progression
Lista de ficheros
Google Scholar:Neves, Maria
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Marolda, Viviana
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Mayor Menéndez, Federico
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Penela Márquez, Petronila
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