Document Detail


Frequent expression of Niban in head and neck squamous cell carcinoma and squamous dysplasia.
MedLine Citation:
PMID:  19536772     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
BACKGROUND: Niban was initially identified in the Eker rat, a model of renal carcinogenesis. We examined Niban expression in head and neck squamous cell carcinoma (HNSCC) and head and neck dysplastic lesions. METHODS: Using a polyclonal rabbit anti-human Niban antibody, 43 cases of HNSCC and 30 cases of head and neck squamous dysplasia were immuonohistochemically stained for Niban. Ancillary genetic studies were also performed. RESULTS: Forty-two of 43 HNSCCs (97.6%) and 20 of 30 (66.6%) dysplastic lesions were positively stained for Niban. The staining was generally less intense in cases of dysplasia than HNSCC. Three of 8 normal mucosal samples from drinker/smokers also showed weak Niban expression. Normal head and neck squamous epithelium from nondrinker/nonsmokers did not stained for Niban. Reverse transcription polymerase chain reaction results matched the immuonohistochemical results. CONCLUSION: The expression of Niban frequently begins in the early stages of head and neck squamous carcinoma and remains upregulated throughout the carcinogenic process. Niban may be a good molecular marker of HNSCC.
Authors:
Shin Ito; Hiroaki Fujii; Toshiharu Matsumoto; Masaaki Abe; Katsuhisa Ikeda; Okio Hino
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Head & neck     Volume:  32     ISSN:  1097-0347     ISO Abbreviation:  Head Neck     Publication Date:  2010 Jan 
Date Detail:
Created Date:  2009-12-17     Completed Date:  2010-04-02     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  8902541     Medline TA:  Head Neck     Country:  United States    
Other Details:
Languages:  eng     Pagination:  96-103     Citation Subset:  IM    
Affiliation:
Department of Otorhinolaryngology, Juntendo University School of Medicine, Tokyo, Japan.
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MeSH Terms
Descriptor/Qualifier:
Animals
Carcinoma, Squamous Cell / genetics*,  pathology
Cell Transformation, Neoplastic / genetics
Gene Expression Regulation, Neoplastic
Head and Neck Neoplasms / genetics*,  pathology
Humans
Hyperplasia / genetics
Immunohistochemistry
Neoplasm Proteins / genetics*
Predictive Value of Tests
Reverse Transcriptase Polymerase Chain Reaction
Sensitivity and Specificity
Tumor Markers, Biological / genetics*
Chemical
Reg. No./Substance:
0/FAM129A protein, human; 0/Neoplasm Proteins; 0/Tumor Markers, Biological

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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