The Novel Role of SOX2 as an Early Predictor of Cancer Risk in Patients with Laryngeal Precancerous Lesions
Autor: | Mario Sánchez-Canteli, Sofía T. Menéndez, Rocío Granda-Díaz, Rene Rodriguez, Daniel Pedregal Mallo, Laura Suárez-Fernández, Aitana Vallina, M. Soledad Fernández-García, Francisco Hermida-Prado, Juan P. Rodrigo, Aida Rodríguez, Juana M. García-Pedrero |
---|---|
Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
Oncology Cancer Research medicine.medical_specialty gene amplification SOX2 medicine.disease_cause lcsh:RC254-282 cancer risk assessment Article Malignant transformation 03 medical and health sciences 0302 clinical medicine dysplasia stomatognathic system Internal medicine Gene duplication medicine Grading (tumors) larynx Cancer prevention business.industry lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens medicine.disease 030104 developmental biology Dysplasia Tumor progression 030220 oncology & carcinogenesis immunohistochemistry embryonic structures Immunohistochemistry Carcinogenesis business |
Zdroj: | Cancers Volume 11 Issue 3 Scopus RUO. Repositorio Institucional de la Universidad de Oviedo instname Cancers, Vol 11, Iss 3, p 286 (2019) |
ISSN: | 2072-6694 |
DOI: | 10.3390/cancers11030286 |
Popis: | The SOX2 gene located at 3q26 is frequently amplified and overexpressed in multiple cancers, including head and neck squamous cell carcinomas (HNSCC). The tumor-promoting activity and involvement of SOX2 in tumor progression has been extensively demonstrated, thereby emerging as a promising therapeutic target. However, the role of SOX2 in early stages of tumorigenesis and its possible contribution to malignant transformation remain unexplored. This study investigates for the first time SOX2 protein expression by immunohistochemistry and gene amplification by real-time PCR using a large series of 94 laryngeal precancerous lesions. Correlations with the histopathological classification and the risk of progression to invasive carcinoma were established. Nuclear SOX2 expression was frequently detected in 38 (40%) laryngeal dysplasias, whereas stromal cells and normal adjacent epithelia showed negative expression. SOX2 gene amplification was detected in 18 (33%) of 55 laryngeal dysplasias. Univariate Cox analysis showed that SOX2 gene amplification (p = 0.046) and protein expression (p < 0.001) but not histological grading (p = 0.432) were significantly associated with laryngeal cancer risk. In multivariate stepwise analysis including age, tobacco, histology, SOX2 gene amplification and SOX2 expression, SOX2 expression (HR = 3.531, 95% CI 1.144 to 10.904 p = 0.028) was the only significant independent predictor of laryngeal cancer development. These findings underscore the relevant role of SOX2 in early tumorigenesis and a novel clinical application of SOX2 expression as independent predictor of laryngeal cancer risk in patients with precancerous lesions beyond current WHO histological grading. Therefore, targeting SOX2 could lead to effective strategies for both cancer prevention and treatment. |
Databáze: | OpenAIRE |
Externí odkaz: | |
Nepřihlášeným uživatelům se plný text nezobrazuje | K zobrazení výsledku je třeba se přihlásit. |