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E-Cadherin gene expression in oral cancer: clinical and prospective data

    1. [1] Universidad de Guadalajara

      Universidad de Guadalajara

      México

    2. [2] Universidad Autónoma de Zacatecas

      Universidad Autónoma de Zacatecas

      México

    3. [3] Universidad Juárez del Estado de Durango

      Universidad Juárez del Estado de Durango

      México

    4. [4] Universidad Autónoma Metropolitana

      Universidad Autónoma Metropolitana

      México

    5. [5] Universidad de la República

      Universidad de la República

      Uruguay

  • Localización: Medicina oral, patología oral y cirugía bucal. Ed. inglesa, ISSN-e 1698-6946, Vol. 24, Nº. 4 (July), 2019
  • Idioma: inglés
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  • Resumen
    • Low protein expression of E-cadherin in oral squamous cell carcinoma (OSCC) has been associated with clinical and histopathological traits such as metastases, recurrence, low survival and poor tumor differentiation, and it is considered a high-risk marker of malignancy. However, it is still unknown whether low expression of E-cadherin is also present at the mRNA level in OSCC cases. Objective: The aim of this study was to compare E-cadherin mRNA expression in OSCC patients and controls and to correlate the expression with clinical and prospective characteristics.

      Forty patients and 40 controls were enrolled. E-cadherin mRNA expression was evaluated by quantitative real-time polymerase chain reaction using TaqMan probes.

      E-cadherin mRNA expression was significantly decreased in OSCC patients compared to that of controls (p<0.001). Whereas no significant association between clinical parameters and E-cadherin expression levels was observed, we noted lower E-cadherin expression levels in patients with positive lymph node metastasis.

      E-cadherin mRNA expression was markedly diminished in OSCC, in agreement with previous results that examined E-cadherin expression at the protein level. E-cadherin is downregulated in the early clinical stages of OSCC, and its mRNA levels do not change significantly in the advanced stages, suggesting that there is limited usefulness of this parameter for predicting disease progression.


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