The Inhibition of the FGFR/PI3K/Akt Axis by AZD4547 Disrupts the Proangiogenic Microenvironment and Vasculogenic Mimicry Arising from the Interplay between Endothelial and Triple-Negative Breast Cancer Cells

Vasculogenic mimicry (VM), a process in which aggressive cancer cells form tube-like structures, plays a crucial role in providing nutrients and escape routes. Highly plastic tumor cells, such as those with the triple-negative breast cancer (TNBC) phenotype, can develop VM. However, little is known...

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Bibliographic Details
Published in:International journal of molecular sciences 2023-09, Vol.24 (18), p.13770
Main Authors: Morales-Guadarrama, Gabriela, Méndez-Pérez, Edgar A, García-Quiroz, Janice, Avila, Euclides, Ibarra-Sánchez, María J, Esparza-López, José, García-Becerra, Rocío, Larrea, Fernando, Díaz, Lorenza
Format: Article
Language:English
Subjects:
Analysis
Angiogenesis
Breast cancer
Cancer cells
Cells
Diagnostic reagents industry
Endothelium
Growth factors
Hypoxia
Kinases
Localization
Metabolism
Morphology
Participation
Vascular endothelial growth factor
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Summary:Vasculogenic mimicry (VM), a process in which aggressive cancer cells form tube-like structures, plays a crucial role in providing nutrients and escape routes. Highly plastic tumor cells, such as those with the triple-negative breast cancer (TNBC) phenotype, can develop VM. However, little is known about the interplay between the cellular components of the tumor microenvironment and TNBC cells’ VM capacity. In this study, we analyzed the ability of endothelial and stromal cells to induce VM when interacting with TNBC cells and analyzed the involvement of the FGFR/PI3K/Akt pathway in this process. VM was corroborated using fluorescently labeled TNBC cells. Only endothelial cells triggered VM formation, suggesting a predominant role of paracrine/juxtacrine factors from an endothelial origin in VM development. Via immunocytochemistry, qPCR, and secretome analyses, we determined an increased expression of proangiogenic factors as well as stemness markers in VM-forming cancer cells. Similarly, endothelial cells primed by TNBC cells showed an upregulation of proangiogenic molecules, including FGF, VEGFA, and several inflammatory cytokines. Endothelium-dependent TNBC-VM formation was prevented by AZD4547 or LY294002, strongly suggesting the involvement of the FGFR/PI3K/Akt axis in this process. Given that VM is associated with poor clinical prognosis, targeting FGFR/PI3K/Akt pharmacologically may hold promise for treating and preventing VM in TNBC tumors.
ISSN:1422-0067
1661-6596
1422-0067
DOI:10.3390/ijms241813770