Dysregulation and detection methods of EGFR in oral cancer. A narrative review.

  • Carolina Somarriva Facultad de Odontología, Universidad Andrés Bello.
  • Alejandra Fernández Facultad de Odontología, Universidad Andrés Bello. Centro de Investigación Biomédica, Universidad de Los Andes.
  • Jorge Candia Facultad de Odontología, Universidad Andrés Bello.
  • Javier Campos Centro de Investigación Biomédica, Universidad de Los Andes.
  • Daniela Albers Centro de Investigación Biomédica, Universidad de Los Andes. Facultad de Odontología, Universidad Mayor.
  • Jorge Briceño Facultad de Odontología, Universidad Andrés Bello.

Abstract

Epidermal growth factor receptor (EGFR) is a transmembrane glycoprotein, with an intracellular domain and tyrosine kinase function (TK) involved in cell proliferation. Dysfunctions in EGFR signaling pathways have been associated with oral malignant tumors such as oral squamous cell carcinoma (OSCC). Dysfunctions of EGFR may result from: increased EGF ligand; EGFR overexpression and copy number gain of the EGFR gene (EGFR CNG); EGFR mutations; failure in the downregulation of EGFR; and EGFR crosstalk. Of these alterations, overexpression of EGFR is by far the most studied dysfunction in OSCC. Clinicians should identify possible alterations of EGFR in the oral mucosa of patients, as EGFR can act as a biomarker for the diagnosis and prognosis of OSCC. Currently, there are several methods and techniques for detecting EGFR. Immunohistochemistry (IHC), fluorescence in situ hybridization (FISH) and polymerase chain reaction (PCR), are used to identify overexpression of EGFR, EGFR CNG and EGFR mutations, respectively. Detection of EGFR as a biomarker is key to identify any oral malignant transformation. Consequently, it becomes imperative to implement a non-invasive and inexpensive method of early diagnosis for OSCC in clinical practice.

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Published
2016-11-09
How to Cite
SOMARRIVA, Carolina et al. Dysregulation and detection methods of EGFR in oral cancer. A narrative review.. Journal of Oral Research, [S.l.], v. 5, n. 7, p. 285-292, nov. 2016. ISSN 0719-2479. Available at: <https://www.joralres.com/index.php/JOralRes/article/view/joralres.2016.057>. Date accessed: 03 may 2024. doi: https://doi.org/10.17126/joralres.2016.057.
Section
Reviews

Keywords

Epidermal Growth Factor Receptor; Mouth Neoplasm; Mutation.

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