SPINK7 expression changes accompanied by HER2, P53 and RB1 can be relevant in predicting oral squamous cell carcinoma at a molecular level
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2021Metadata
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Pennacchiotti Vidal, Gina Fabiola
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SPINK7 expression changes accompanied by HER2, P53 and RB1 can be relevant in predicting oral squamous cell carcinoma at a molecular level
Author
- Pennacchiotti Vidal, Gina Fabiola;
- Valdés Gutiérrez, Fabio;
- González Arriagada, Wilfredo Alejandro;
- Montes, Héctor Federico;
- Parra, Judith María Roxana;
- Guida, Valeria Andrea;
- Gómez, Silvina Esther;
- Guerrero Giménez, Martín Eduardo;
- Fernández Muñoz, Juan Manuel;
- Martin Zoppino, Felipe Carlos;
- Carón, Rubén Walter;
- Ezquer, Marcelo Eduardo;
- Fernández Ramires, Ricardo;
- Bruna, Flavia Alejandra;
Abstract
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.
Patrocinador
Foundation JA Roemmers
Project FDP Universidad Mayor RFR PEP I-2019081
Comision Nacional de Investigacion Cientifica y Tecnologica (CONICYT)
CONICYT FONDECYT 11140281
PI UDD-CAS N20141001185304708249
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Artículo de publícación WoS Artículo de publicación SCOPUS
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Scientific Reports (2021) 11:6939
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