ISRN Pathology · 2012 · 14 citations · 12 references
MedicineOncologyOral PathologyCarcinogenesisNeoplasiaOral OncologyChemical CarcinogenesisExtracellular MatrixOral CarcinogenesisOral Cavity CancerOral NeoplasiaSquamous Cell CarcinomaConnective Tissue DevelopmentConnective Tissue MatrixExtracellular Matrix InductionExtracellular Matrix NetworksHistochemical MarkersImmunohistochemical StainingOral Epithelial CarcinogenesisOral Lesion Malignant Transformation
Introduction . Oral squamous cell carcinoma (OSCC) is one of the ten most common cancers affecting the human population. Tumor pathogenesis implies a multistep process in which cells acquire features that enable them to become tumorigenic and ultimately malignant. The process of OSCC carcinogenesis can be reproduced in animal models, the OSCC induction with 4-nitroquinoline-1-oxide (4NQO) in mice is a widely used tool for studying tumor pathogenesis. Objective . The aim of the present study was to determine the progressive changes in basal lamina and connective tissue remodeling during 4NQO-induced OSCC carcinogenesis. Material and Methods . Samples were classified according to “International Histological Classification of tumors” in mild, moderate, and severe dysplasia and invasive carcinoma. Five samples of each pathologic entity and control healthy tongues were used. Immunohistochemical analysis of collagen IV as well as histochemical analysis of glycosylated molecules (PAS) and collagen I (Picro Sirius red) were performed. Results . During experimental-induced carcinogenesis by 4NQO a progressive basal lamina destruction and collagen I disorganization in adjacent connective tissue can be observed. Conclusion . Our results confirm previous studies that show alterations in extracellular matrix (ECM) in malignant lesions, validating the experimental carcinogenesis induced by 4NQO.
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Oral Cavity and Esophageal Carcinogenesis Modeled in Carcinogen-Treated Mice
Xiao‐Han Tang, Beatrice S. Knudsen, Debra L. Bemis et al. · Clinical Cancer Research · 2004 · 394 citations
Medicine, Cancer Biology, Oncology +13