Determination of cytokine profile and associated genes of the signaling pathway in HNSCC

J Recept Signal Transduct Res. 2022 Oct;42(5):462-468. doi: 10.1080/10799893.2021.2013888. Epub 2021 Dec 9.

Abstract

Head and neck squamose cell carcinoma (HNSCC) is an aggressive group of tumors that are generally heterogeneous. Despite treatment advances, disease-free survival has not significantly improved. Therefore, it is of great importance to understand the molecular etiology of HNSCC and genetic alterations in the signal pathways in order to develop new therapeutic approaches. In this study, firstly we used a cytokine array to analyze the secretomes of HNSCC patients and healthy controls. In the next step, the results from the cytokine sequence were validated by qRT-PCR and western blot, including genes in the associated signaling pathway. In array analysis, the levels of EGF, IGF-1, IGFBP-1, and PDGFBB were significantly higher in patients than in the controls. The results of qRT-PCR analyses showed that expression levels of PDGFRB gene were significantly up-regulated (p = 0.006) and PTEN (p > 0.001) were significantly down-regulated in tumors compared with normal tissues. When groups (early vs. advanced) were compared, higher expression of IGFBP-1 was observed in the larynx (p = 0.045) and larynx + oral cavity tumors (p = 0.010) in an advanced stage. In western blot analysis, pEGFR, pIGF-IR, pIR-β, pPDGFRB, and pAKT levels were upregulated, and pPTEN was downregulated in tumors. Based on our observations, determining the interactions of EGFR, PDGFRB, IGF-1R and PTEN or the activation of each might represent a promising new and innovative treatment approach in HNSCC patients. It seems clear that, in most cancers, effective targeted therapy may be involved the blockade of each one or multiple targets.

Keywords: Head and neck squamose cell carcinoma; cytokines; receptors; signal pathways.

MeSH terms

  • Carcinoma, Squamous Cell* / pathology
  • Cell Line, Tumor
  • Cytokines / genetics
  • Cytokines / metabolism
  • Epidermal Growth Factor
  • ErbB Receptors / genetics
  • ErbB Receptors / metabolism
  • Female
  • Head and Neck Neoplasms* / genetics
  • Humans
  • Insulin-Like Growth Factor Binding Protein 1 / metabolism
  • Insulin-Like Growth Factor Binding Protein 1 / therapeutic use
  • Insulin-Like Growth Factor I / genetics
  • Insulin-Like Growth Factor I / metabolism
  • Placenta Growth Factor / metabolism
  • Placenta Growth Factor / therapeutic use
  • Receptor, Platelet-Derived Growth Factor beta
  • Signal Transduction / genetics
  • Squamous Cell Carcinoma of Head and Neck / genetics

Substances

  • Cytokines
  • Insulin-Like Growth Factor Binding Protein 1
  • Placenta Growth Factor
  • Epidermal Growth Factor
  • Insulin-Like Growth Factor I
  • ErbB Receptors
  • Receptor, Platelet-Derived Growth Factor beta