transforming-growth-factor-alpha and Respiratory-Tract-Neoplasms

The enhanced proliferation of epithelial cells is a typical feature of respiratory papilloma. The mechanism or mechanisms leading to abnormal epithelial proliferation remain unclear. Overexpression of growth factors and their receptors and inactivation of tumor-suppressor proteins are known to cause cell transformation and proliferation. The objectives of this study were to evaluate the expression of these factors in juvenile respiratory papillomas with correlation to cellular proliferation activity, and to determine whether such expression is associated with the clinical course of the disease. The expression of transforming growth factor-alpha, epidermal growth factor receptor, p53 protein, retinoblastoma proteins and Ki-67 was quantified by immunohistochemistry in paraffin-embedded biopsy specimens taken at the initial surgical excision from children in whom respiratory papillomatosis was diagnosed. Clinical information regarding the number of disease sites, tracheobronchial spread, malignant transformation, and frequency of recurrences was reviewed. Thirty-five specimens were suitable for immunohistochemical evaluation. Ki-67 expression was significantly higher in patients with multiple sites of disease and frequent recurrences. High p53 expression was significantly associated with malignant transformation. We concluded that Ki-67 and p53 expression may be predictive of the clinical course in children with respiratory papillomatosis.

Topics: Adolescent; Biomarkers, Tumor; Cell Division; Cell Transformation, Neoplastic; Child; ErbB Receptors; Female; Humans; Immunoenzyme Techniques; Ki-67 Antigen; Male; Neoplasm Invasiveness; Neoplasm Recurrence, Local; Papilloma; Prognosis; Respiratory Mucosa; Respiratory Tract Neoplasms; Retinoblastoma Protein; Transforming Growth Factor alpha; Tumor Suppressor Protein p53