Home

search

Subjectguide
Journals
Books / Serials / Multimedia
Services
Services

Login for Subscribers
Logout

Sitemap
Help
Contacts


Logo






Vol. 69, No. 4, 2007   

Free Abstract     Article (References)     Article (PDF 163 KB)     

Original Paper

Downregulation of Fanconi Anemia Genes in Sporadic Head and Neck Squamous Cell Carcinoma
Volkert B. Wreesmanna, Cherry Estilob, David W. Eiselea, Bhuvanesh Singhb, Steven J. Wanga

aDepartment of Otolaryngology - Head and Neck Surgery, University of California, San Francisco, Calif., and
bHead and Neck Service, Memorial Sloan-Kettering Cancer Center, New York, N.Y., USA

Address of Corresponding Author

ORL 2007;69:218-225 (DOI: 10.1159/000101542)


 goto top of page Key Words

  • Fanconi anemia
  • Head and neck cancer
  • Squamous cell carcinoma
  • Real-time polymerase chain reaction

 goto top of page Abstract

Background/Aims: Much of our understanding of human cancer has come from studies of the hereditary cancer predisposition syndromes. Fanconi anemia (FA) is an autosomal recessive disorder characterized by cellular hypersensitivity to DNA crosslinking agents, progressive bone marrow failure, and cancer predisposition to solid malignancies, especially head and neck squamous cell carcinoma (HNSCC). Since FA pathway-deficient cells are hypersensitive to DNA crosslinking chemotherapy agents, the presence of somatic FA gene inactivation in sporadic cancers may be of clinical interest. This study sought to determine the frequency of FA gene downregulation in sporadic HNSCC. Methods: The expression of the FA genes FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCJ, FANCL and FANCM in 11 HNSCC cell lines and 49 tongue carcinoma samples was studied with quantitative real-time polymerase chain reaction. Results: Downregulation of at least one FA gene was observed in 3 of 11 HNSCC cell lines and 66% of tongue carcinoma samples. FANCB, FANCF, FANCJ and FANCM were most commonly affected by downregulation, whereas downregulation of FANCA, FANCE and FANCD2 was rare. Conclusion: Our data suggest that downregulation of FA genes is common in sporadic HNSCC. The clinical implications of this finding merit further study.

Copyright © 2007 S. Karger AG, Basel


 goto top of page Author Contacts

Steven J. Wang, MD
4150 Clement St., 112B
San Francisco, CA 94121 (USA)
Tel. +1 415 221 4810, ext. 4646, Fax +1 415 750 2181
E-Mail swang@ohns.ucsf.edu


 goto top of page Article Information

Presented at the Annual Meeting of the American Association for Cancer Research, Washington, D.C., April 4, 2006.

Received: August 31, 2006
Accepted after revision: October 14, 2006
Published online: April 4, 2007
Number of Print Pages : 8
Number of Figures : 2, Number of Tables : 3, Number of References : 25

 
Journal Home
Journal Content
Guidelines
Editorial Board
Aims and Scope
Subscriptions
Medline Abstract (ID 17409780)
Download Citation




For non-native English speakers and international authors who would like assistance with their writing before submission, we suggest American Journal Experts for their scientific editing service.





copyright  © 2009 S. Karger AG, Basel