Using LongSAGE to Detect Biomarkers of Cervical Cancer Potentially Amenable to Optical Contrast Agent Labelling

Author:

Kneller Julie M.1,Ehlen Thomas2,Matisic Jasenka P.3,Miller Dianne2,Van Niekerk Dirk4,Lam Wan L.5,Marra Marco1,Richards-Kortum Rebecca6,Follen Michelle7,MacAulay Calum3,Jones Steven J.M.1

Affiliation:

1. Genome Sciences Centre, British Columbia Cancer Research Centre, Vancouver, BC, Canada.

2. Department of Gynaecologic Oncology, British Columbia Cancer Agency, Vancouver, BC, Canada.

3. Cancer Imaging, British Columbia Cancer Research Centre, Vancouver, BC, Canada.

4. Cervical Cancer Screening Program, British Columbia Cancer Agency, Vancouver, BC, Canada.

5. Cancer Genetics and Developmental Biology, British Columbia Cancer Research Centre, Vancouver, BC, Canada.

6. Biomedi-cal Engineering, University of Texas at Austin, Austin, TX, U.S.A.

7. University of Texas M.D. Anderson Cancer Center, Department of Gynecologic Oncology and Biomedical Engineering Center, Houston, TX, U.S.A.

Abstract

Sixteen longSAGE libraries from four different clinical stages of cervical intraepithelial neoplasia have enabled us to identify novel cell-surface biomarkers indicative of CIN stage. By comparing gene expression profiles of cervical tissue at early and advanced stages of CIN, several genes are identified to be novel genetic markers. We present fifty-six cell-surface gene products differentially expressed during progression of CIN. These cell surface proteins are being examined to establish their capacity for optical contrast agent binding. Contrast agent visualization will allow real-time assessment of the physiological state of the disease process bringing vast benefit to cancer care. The data discussed in this publication have been submitted to NCBIs Gene Expression Omnibus (GEO, http://www.ncbi.nlm.nih.gov/geo/ ) and are accessible through GEO Series accession number GSE6252.

Publisher

SAGE Publications

Subject

Biochemistry, medical,Pharmacology,Molecular Medicine

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