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1.
Journal of the Korean Association of Oral and Maxillofacial Surgeons ; : 101-109, 2012.
Article in English | WPRIM | ID: wpr-229229

ABSTRACT

OBJECTIVES: The inactivation of the tumor suppressor gene p16INK4a plays an important role in the development of malignant tumors, including oral squamous cell carcinoma. The p16 gene is involved in the p16/cyclin-dependent kinase/retinoblastoma (Rb) gene pathway of cell cycle control. The p16 protein is considered a negative regulator of this pathway. The p16 gene encodes an inhibitor of cyclin-dependent kinases 4 and 6 which regulate the phosphorylation of the retinoblastoma gene and G1 to S phase transition in the cell cycle. However, the p16 gene can lose its functionality through point mutations, loss of heterozygosity or methylation of its promoter region. MATERIALS AND METHODS: In this study, the authors analyzed the correlation between various clinicopathological findings-patient age, gender and smoking, disease recurrence, tumor size, stage, and differentiation- and p16 protein expression or p16 promoter hypermethylation in 59 cases of head and neck squamous cell carcinoma. RESULTS: The results revealed p16 protein expression and p16 promoter hypermethylation in 28 cases (47.5%) and 21 cases (35.6%), respectively, of head and neck squamous cell carcinoma. However, neither p16 protein expression nor p16 promoter hypermethylation had any statistical influence on clinicopathological findings or survival rate. CONCLUSION: This data, and a review of the literature, suggest that p16 promoter hypermethylation cannot yet be used as an independent prognostic factor influencing carcinogenesis, but must be considered as an important factor along with other genetic alterations affecting the pRb pathway.


Subject(s)
Humans , Carcinoma, Squamous Cell , Cell Cycle , Cell Cycle Checkpoints , Cyclin-Dependent Kinases , Epigenomics , Genes, p16 , Genes, Retinoblastoma , Genes, Tumor Suppressor , Head , Loss of Heterozygosity , Methylation , Neck , Phosphorylation , Point Mutation , Prognosis , Recurrence , S Phase , Smoke , Smoking
2.
Journal of the Korean Association of Oral and Maxillofacial Surgeons ; : 468-473, 2001.
Article in Korean | WPRIM | ID: wpr-117734

ABSTRACT

Castleman's disease or angiofollicular lymph node hyperplasia, is a rare lymphoproliferative disorder. It may be appear as a local or generalized tumor-like condition, usually in chest or abdomen and may involve both lymph nodes and non-nodal tissues. Castleman's disease is an unusal entity which may at times mimic malignancy but is entirely benign in nature. It is topical as it has been noted to occur with AIDS and Kaposi's sarcoma. Careful interpretation of radiogram may help to distinguish Castleman's disease from other tumor condition, such as lymphoma, neurogenic tumor, or even angiofibroma, etc. But exact diagnosis must be made on the basis of histologic confirmation. In addition to histologic features, clinical distinction between the localized and multicentric form is important in selecting appropriate management. Surgical excision of an localized mass is the first choice of treatment. Partial resection, radiotherapy or observation alone may avoid the need for exessively aggressive therapy. Patients with multicentric disease don't benefit by surgical management because of systemic manifestation and rapid deterioration. Thus, antineoplastic agents and steroids may offer an alternative form of therapy. We report a case of female patient with Castleman's disease in oral and maxillofacial region, treated by surgical excision with good results.


Subject(s)
Female , Humans , Abdomen , Angiofibroma , Antineoplastic Agents , Diagnosis , Castleman Disease , Lymph Nodes , Lymphoma , Lymphoproliferative Disorders , Radiotherapy , Sarcoma, Kaposi , Steroids , Thorax
3.
Journal of the Korean Association of Maxillofacial Plastic and Reconstructive Surgeons ; : 353-359, 1999.
Article in Korean | WPRIM | ID: wpr-784211
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