The ATM tumour suppressor gene is down‐regulated in EBV‐associated nasopharyngeal carcinoma |
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Authors: | Shikha Bose Lee‐Fah Yap Matthew Fung Jane Starzcynski Amyza Saleh Susan Morgan Christopher Dawson Marilyn B Chukwuma Esther Maina Maike Buettner Wenbin Wei John Arrand Paul VH Lim Lawrence S Young Soo Hwang Teo Tatjana Stankovic Ciaran BJ Woodman Paul G Murray |
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Affiliation: | 1. Cancer Research UK Institute for Cancer Studies, University of Birmingham, Birmingham B15 2TT, UK;2. These two authors contributed equally.;3. Cancer Research Initiatives Foundation (CARIF), 2nd Floor Outpatient Centre, Subang Jaya Medical Centre, 47500 Subang Jaya, Selangor, Malaysia;4. Birmingham Heartlands Hospital, Birmingham B9 5SS, UK;5. Institut für Pathologie, Friedrich‐Alexander‐University, Krankenhausstrasse 22, 91054 Erlangen, Germany;6. Tung Shin Hospital, Kuala Lumpur, Malaysia |
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Abstract: | A micro‐array analysis using biopsies from patients with EBV‐positive undifferentiated nasopharyngeal carcinoma (NPC) and from cancer‐free controls revealed down‐regulation of tumour suppressor genes (TSG) not previously associated with this disease; one such gene was the ataxia telangiectasia mutated (ATM) gene. Q‐PCR confirmed down‐regulation of ATM mRNA and ATM protein expression in tumour cells was weak or absent in almost all cases. In NPC cell lines, however, ATM was down‐regulated only in the EBV‐positive line, C666.1, and in none of five EBV‐negative lines. In vitro infection of EBV‐negative NPC cell lines with a recombinant EBV was followed by the down‐regulation of ATM mRNA and protein, and only EBV‐positive cells showed a defective DNA damage response following γ‐irradiation. Our data suggest that loss of ATM function could be an important step in the pathogenesis of NPC, and may have implications for the treatment of this disease. Copyright © 2008 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd. |
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Keywords: | nasopharyngeal carcinoma ATM Epstein– Barr virus |
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