Oral Oncology
Volume 40, Issue 5 , Pages 511-519, May 2004

OCGR array: an oral cancer genomic regional array for comparative genomic hybridization analysis

  • Cathie Garnis

      Affiliations

    • British Columbia Cancer Research Centre, 601 West 10th Avenue, Vancouver, BC, Canada V5Z 1L3
    • Departments of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada V6T 2B5
    • Corresponding Author InformationCorresponding author. Address: British Columbia Cancer Research Centre, 601 West 10th Avenue, Vancouver, BC, Canada V5Z 1L3. Tel.: +1-604-877-6149; fax: +1-604-877-6155
  • ,
  • Jennifer Campbell

      Affiliations

    • British Columbia Cancer Research Centre, 601 West 10th Avenue, Vancouver, BC, Canada V5Z 1L3
  • ,
  • Lewei Zhang

      Affiliations

    • Oral Biological and Medical Sciences, University of British Columbia, Vancouver, BC, Canada V6T 2B5
  • ,
  • Miriam P Rosin

      Affiliations

    • British Columbia Cancer Research Centre, 601 West 10th Avenue, Vancouver, BC, Canada V5Z 1L3
  • ,
  • Wan L Lam

      Affiliations

    • British Columbia Cancer Research Centre, 601 West 10th Avenue, Vancouver, BC, Canada V5Z 1L3
    • Departments of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada V6T 2B5

Received 29 September 2003; accepted 22 October 2003.

Abstract 

Genetic alterations have been recognized as important events in the carcinogenesis of oral squamous cell carcinoma (OSCC) and have been used as predictors of progression risk. In this study, we have designed an oral cancer-specific human bacterial artificial chromosome (BAC) array, called the oral cancer genomic regional array (OCGR), to detect and fine map copy number alterations in OSCC. This array contains a total of ∼45 Mbp coverage of nine chromosomal regions reported to be involved in the progression of oral cancer. We demonstrate the detection of copy number alterations in 14 microdissected clinical specimens in each of the nine regions. These include both copy number increases and decreases. Although the number of regions selected for this first generation array is small, we observed multiple segmental changes. In some cases, we observed single BAC clone alterations at 7p11 and 11q13 which contain EGFR and cyclin D1 respectively highlighting the need for high resolution detection techniques. Array comparative genomic hybridization (CGH) complements traditional methods for detecting genetic alterations in OSCC (such as microsatellite and CGH analysis) by improving the detection of segmental copy number alterations to single BAC clone resolution. This work represents the first attempt at the construction of an oral cancer-specific CGH array.

Keywords:  Oral, Head and neck, Progression, Array CGH, Profiling, Copy number, Microamplification, High resolution, Cancer

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PII: S1368-8375(03)00231-8

doi:10.1016/j.oraloncology.2003.10.006

Oral Oncology
Volume 40, Issue 5 , Pages 511-519, May 2004