3.8 Article

Frequent allelic imbalances at 8p and 11q22 in oral and oropharyngeal epithelial dysplastic lesions

Journal

CANCER GENETICS AND CYTOGENETICS
Volume 161, Issue 1, Pages 86-89

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.cancergencyto.2005.01.004

Keywords

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Funding

  1. NCI NIH HHS [R21 CA 095231] Funding Source: Medline
  2. NIDCR NIH HHS [R01 DE 015970-01, K22 DE 014847] Funding Source: Medline

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Allelic imbalance is characteristic of oral squamous cell carcinoma (SCC) and contributes to the tumorigenesis of this disease. Our previous studies suggest that chromosome regions 8p and 11q22.2 similar to q22.3 are frequent sites of loss of heterozygosity (LOH) in head and neck SCC. Here, we explored the allelic imbalance pattern of these regions in 27 cases of oral epithelial dysplastic lesions. A previously reported frequent LOH (9p21) in head and neck dysplasia was also examined. Laser capture microdissection (LCM) technology was utilized to harvest homogenous cell populations from archived clinical tissues and thus greatly enhancing the sensitivity, accuracy and reliability of genetic assessment. The allelic imbalance (LOH and microsatellite instability) on 8p, 11q22.2 similar to q22.3, and 9p21 were observed at one or more loci in 66.7 %, 63.0 %, and 63.0 % of cases, respectively. Our results demonstrate that 8p, 11q22.2 similar to q22.3, and 9p21 are frequent allelic imbalance regions in oral premalignant dysplasia and suggest the presence of tumor suppressor genes in these regions. (c) 2005 Elsevier Inc. All rights reserved.

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