Article
Hedgehog pathway activation in oral squamous cell carcinoma: cancer‑associated fibroblasts exhibit nuclear GLI‑1 localization
Registro en:
GUIMARAES, Vanessa Sousa Nazare et al. Hedgehog pathway activation in oral squamous cell carcinoma: cancer‑associated fibroblasts exhibit nuclear GLI‑1 localization. Journal of Molecular Histology, 2020.
1567-2379
10.1007/s10735-020-09913-5
Autor
Guimaraes, Vanessa Sousa Nazare
Vidal, Manuela Torres Andion
Valverde, Ludmila de Faro
Oliveira, Marbele Guimarães de
Rocha, Leonardo de Oliveira Siquara da
Coelho, Paulo Lucas Cerqueira
Soares, Fernando Augusto
Souza, Bruno Solano de Freitas
Bezerra, Daniel Pereira
Coletta, Ricardo D.
Pereira, Thiago Almeida
Santos, Jean Nunes dos
Rocha, Clarissa Araújo Gurgel
Resumen
National Council for Scientific and Technological
Development (CNPq), [Grant No. 308595/2016‐5]. The purpose of this study was to evaluate the expression of Hedgehog (HH) signaling molecules (SHH and GLI-1) by cancerassociated
fibroblasts (CAF) in oral squamous cell carcinoma (OSCC). Immunohistochemistry was used to detect molecular
HH signaling and CAF-related protein expression, including α-SMA and S100A4, in 70 samples of human OSCC. The
colocalization of α-SMA and S100A4 with SHH was also evaluated by double-staining. In vitro study was performed using
primary normal oral fibroblast (NOF) and CAF through immunofluorescence and Western Blot for CAF-proteins, SHH, and
GLI-1. Forty-five cases (64.28%) were positive for α-SMA exclusively in tumor stroma, and S100A4 was identified in the
cytoplasm of CAFs in 94.28% (n = 66) of the cases. With respect to stromal cells, 64 (91.43%) OSCC cases were positive
for SHH, and 31 were positive for GLI-1 (44.29%); positive correlations were found between SHH and α-SMA (p < 0.0001,
φ = 0.51), as well as between SHH and S100A4 (p = 0.087, φ = 0.94). Protein expression of SHH and GLI-1 was observed in
primary CAFs and NOFs. Although SHH was found to be localized in the cellular cytoplasm of both cell types, GLI-1 was
present only in the nuclei of CAF. Our results indicate that CAFs are not only potential sources of HH ligands in tumor stroma,
but may also respond to HH signaling through nuclear GLI-1 activation. We further observed that elevated SHH expression
by OSCC cells was associated with higher CAF density, reinforcing the chemoattractant role played by these molecules.