Publication: Follicle-stimulating hormone promotes nerve growth factor and vascular endothelial growth factor expression in epithelial ovarian cells

Date
2020
Authors
Garrido, Maritza P. ; Bruneau, Nicole ; Vega, Margarita ; Selman, Alberto ; Tapia, Julio C. ; Romero, Carmen
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Publisher
Universidad de Murcia, Departamento de Biologia Celular e Histiologia
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DOI
https://doi.org/10.14670/HH-18-226
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info:eu-repo/semantics/article
Description
Abstract
Ovarian cancer is the first cause of death for
gynecological malignances in developed countries and
around 80% correspond to Epithelial Ovarian Cancer
(EOC). Overexpression of Nerve Growth Factor (NGF)
and its high affinity receptor TRKA are involved in EOC
progression, modulating several oncogenic processes
such as angiogenesis by the increase of Vascular
Endothelial Growth Factor (VEGF). FSH receptors
(FSH-R) are present in EOC, but their changes and
contribution during EOC progression are still not
thoroughly known. The aims of this study were to
evaluate the abundance of FSH receptors during EOC
differentiation and to determine whether FSH modulates
oncoproteins such as NGF and VEGF in ovarian cells.
FSH-R expression in EOC tissues and cell lines (A2780,
poorly differentiated EOC cells and HOSE, non-tumoral
ovarian surface epithelial cells) were measured by RT-
PCR and laser capture of epithelial cells from EOC
samples by qPCR. FSH-R protein levels were evaluated
by immunohisto/cytochemistry. Additionally, ovarian
explants and ovarian cell lines were stimulated with FSH
and/or FSH-R inhibitor to assess NGF and VEGF
mRNA and protein levels.
The results showed that FSH-R levels decreased
during loss of EOC cell differentiation, nevertheless
these receptors are still present in poorly differentiated
EOC. FSH increased NGF expression in ovarian cells,
which was prevented using a FSH-R inhibitor. Similarly,
in ovarian cancer explants, FSH increased NGF and
VEGF mRNA, as well as NGF protein levels. These
results suggest that FSH would display a key role not
only in initial stages of EOC, but also in late stages of
this disease, by modulation of NGF and VEGF levels in
EOC cells
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Citation
Histology and Histopathology Vol. 35, nĀŗ9 (2020)
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