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2.
Br J Oral Maxillofac Surg ; 46(2): 161-2, 2008 Mar.
Article in English | MEDLINE | ID: mdl-17416444

ABSTRACT

A patient presented with a benign schwannoma of the cervical phrenic nerve on the left side of the neck. Analysis of the aspirate suggested the diagnosis and it was confirmed on imaging. The patient had the lesion excised with preservation of the phrenic nerve.


Subject(s)
Head and Neck Neoplasms/pathology , Neurilemmoma/pathology , Peripheral Nervous System Neoplasms/pathology , Phrenic Nerve/pathology , Adult , Biopsy, Needle , Head and Neck Neoplasms/surgery , Humans , Male , Neurilemmoma/surgery , Peripheral Nervous System Neoplasms/surgery , Phrenic Nerve/surgery
3.
Cancer Lett ; 209(2): 207-13, 2004 Jun 25.
Article in English | MEDLINE | ID: mdl-15159023

ABSTRACT

Allelic imbalance on chromosome arm 8p is common in head and neck squamous cell carcinoma (HNSCC). DLC1, a tumour suppressor gene inactivated in liver carcinogenesis and encoding a Rho GTPase activating protein (RhoGAP) maps to one of the deleted regions (8p21.3-22). In order to determine whether inactivation of DLC1 is involved in HNSCC, we have screened tumour cell lines for DLC1 mutations and expression. Pathological mutations were not identified in any of the 17 cell lines tested. Seven polymorphisms were identified; 13 of the 17 of cell lines were homozygous for all seven polymorphisms compared to only 2 of 17 controls suggesting a loss of heterozygosity in a majority of the cell lines. DLC1 expression was observed in all 11 HNSCC cell lines tested, thus excluding the possibility of transcriptional silencing of DLC1 by promoter hypermethylation. Overall, our data suggest that hemizygous deletions of the DLC1 locus are frequent in HNSCCs but this gene is unlikely to be primary target for inactivation on this chromosomal arm.


Subject(s)
Carcinoma, Squamous Cell/genetics , Chromosome Deletion , Chromosomes, Human, Pair 8/genetics , Head and Neck Neoplasms/genetics , Tumor Suppressor Proteins/genetics , Carcinoma, Squamous Cell/pathology , GTPase-Activating Proteins , Head and Neck Neoplasms/pathology , Humans , Loss of Heterozygosity , Microsatellite Repeats , Mutation , Polymorphism, Genetic , Tumor Cells, Cultured , Tumor Suppressor Proteins/metabolism
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