Participation of hypoxia-inducible factor-1α and lymphangiogenesis in metastatic and non-metastatic lower lip squamous cell carcinoma

• Published in: Journal of cranio-maxillo-facial surgery Vol. 46; no. 10; pp. 1741 - 1747
• Main Authors: de Aquino Martins, Ana Rafaela Luz, Santos, Hellen Bandeira de Pontes, Mafra, Rodrigo Porpino, Nonaka, Cassiano Francisco Weege, Souza, Lélia Batista de, Pinto, Leão Pereira
• Format: Journal Article
• Language: English
• Published: Scotland Elsevier Ltd 01-10-2018
• Subjects: Carcinoma, Squamous Cell - metabolism; Carcinoma, Squamous Cell - mortality; Carcinoma, Squamous Cell - pathology; Dentistry; Humans; Hypoxia-Inducible Factor 1, alpha Subunit - metabolism; Hypoxia-inducible factor-1α; Immunohistochemistry; Lip - metabolism; Lip - pathology; Lip Neoplasms - metabolism; Lip Neoplasms - mortality; Lip Neoplasms - pathology; Lymphangiogenesis; Squamous cell carcinoma; Survival Analysis; Immunohistochemistry; Hypoxia-inducible factor-1α; Squamous cell carcinoma; Lymphangiogenesis
• ISSN: 1010-5182; 1878-4119
• DOI: 10.1016/j.jcms.2018.07.020

This study evaluated the lymphatic density and HIF-1α immunoexpression in lower lip squamous cell carcinoma (LLSCC) and their correlation with clinicopathological (nodal metastasis, clinical stage, histological grade, recurrence and disease outcome) and survival parameters in 20 metastatic and 20 non-metastatic LLSCCs. Lymphatic density was established by counting microvessels (D2-40+) at the tumor core (intratumoral lymphatic density, ILD) and at the invasive front (peritumoral lymphatic density, PLD) and percentages of immunopositive cells for HIF-1α were established. No statistically significant differences in lymphatic densities in relation to clinicopathological parameters were observed (P > 0.05). All cases exhibited nuclear and cytoplasmic HIF-1α immunoexpression, with relatively high percentages of positivity, but this expression was not statistically different in relation to clinicopathological variables (P > 0.05). Positive correlations were observed between ILD and PLD (P = 0.002), and between nuclear HIF-1α immunoexpression at the tumor core and ILD (P = 0.001). The results suggest ILD and PLD are not directly related to the development of lymph node metastasis in LLSCC. The striking expression of HIF-1α suggests the involvement of this protein in the etiopathogenesis of LLSCCs, possibly stimulating lymphangiogenesis at the tumor core. However, this protein does not seem to exert a determining influence on the biological aggressiveness of these tumors.