Scientific Reports (Mar 2021)

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

DOI
https://doi.org/10.1038/s41598-021-86208-z
Journal volume & issue
Vol. 11, no. 1
pp. 1 – 11

Abstract

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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.