SPINK7 expression changes accompanied by HER2, P53 and RB1 can be relevant in predicting oral squamous cell carcinoma at a molecular level

Gina Pennacchiotti, Fabio Valdés-Gutiérrez, Wilfredo Alejandro González-Arriagada, Héctor Federico Montes, Judith Maria Roxana Parra, Valeria Andrea Guida, Silvina Esther Gómez, Martin Eduardo Guerrero-Gimenez, Juan Manuel Fernandez-Muñoz, Felipe Carlos Martin Zoppino, Rubén Walter Carón, Marcelo Eduardo Ezquer, Ricardo Fernández-Ramires, Flavia Alejandra Bruna

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

10 Citas (Scopus)


The oral squamous cell carcinoma (OSCC), which has a high morbidity rate, affects patients worldwide. Changes in SPINK7 in precancerous lesions could promote oncogenesis. Our aim was to evaluate SPINK7 as a potential molecular biomarker which predicts OSCC stages, compared to: HER2, TP53, RB1, NFKB and CYP4B1. This study used oral biopsies from three patient groups: dysplasia (n = 33), less invasive (n = 28) and highly invasive OSCC (n = 18). The control group consisted of clinically suspicious cases later to be confirmed as normal mucosa (n = 20). Gene levels of SPINK7, P53, RB, NFKB and CYP4B1 were quantified by qPCR. SPINK7 levels were correlated with a cohort of 330 patients from the TCGA. Also, SPINK7, HER2, TP53, and RB1, were evaluated by immunohistofluorescence. One-way Kruskal-Wallis test and Dunn's post-hoc with a p < 0.05 significance was used to analyze data. In OSCC, the SPINK7 expression had down regulated while P53, RB, NFKB and CYP4B1 had up regulated (p < 0.001). SPINK7 had also diminished in TCGA patients (p = 2.10e-6). In less invasive OSCC, SPINK7 and HER2 proteins had decreased while TP53 and RB1 had increased with respect to the other groups (p < 0.05). The changes of SPINK7 accompanied by HER2, P53 and RB1 can be used to classify the molecular stage of OSCC lesions allowing a diagnosis at molecular and histopathological levels.

Idioma originalInglés
Número de artículo6939
Páginas (desde-hasta)6939
PublicaciónScientific Reports
EstadoPublicada - 1 dic. 2021

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Funding Information:
This work was supported by: PI UDD-CAS N20141001185304708249 grant (FAB); Foundation JA Roemmers (FAB) and Project FDP Universidad Mayor RFR (PEP I-2019081) (RFR) and Project FONDECYT n 11140281 (RFR).

Publisher Copyright:
© 2021, The Author(s).


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