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Telomerase inhibition and the future management of head-and-neck cancer - 01/09/11

Doi : 10.1016/S1470-2045(02)00729-5 
James A McCaul, Dr a,  : Clinical Research Fellow and Specialist Registrar in Maxillofacial surgery, Katrina E Gordon a : Research Fellow, Louise J Clark b : Consultant Otolaryngologist, E Kenneth Parkinson a : Research Group Leader
a Beatson Institute for Cancer Research, Glasgow, UK 
b Victoria Infirmary, Glasgow, UK 

* Correspondence: Dr James A McCaul, Beatson Institute for Cancer Research, Garscube Estate, Switchback Road, Glasgow G61 1BD, UK. Tel: +44 (0) 141 330 3698. Fax: +44 (0) 141 942 6521

Summary

Telomeres are tandem repeats of DNA associated with specific proteins. These structures cap eukaryotic chromosomes and maintain the integrity of the chromosome ends. In the germline, telomeres are maintained by the enzyme telomerase, but in normal somatic cells the enzyme’s activity is low or undetectable. Human tumours, including squamous-cell carcinoma of the head and neck (SCCHN), need telomerase to maintain telomere function; inhibition of the enzyme can lead to apoptosis. Furthermore, because most tumour cells have very short telomeres, they are more likely to succumb to telomerase inhibition than normal cells. Telomerase is therefore a potential selective anticancer target. The telomere is also involved in the repair of DNA double strand breaks, and telomere dysfunction provokes radiosensitivity. In this review we consider whether manipulation of telomere function may selectively sensitise SCCHN to radiotherapy and discuss the possible pitfalls. We also assess how some conventional treatments may affect the subsequent use of telomerase inhibitors.

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© 2002  Elsevier Ltd. Reservados todos los derechos.
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Vol 3 - N° 5

P. 280-288 - mai 2002 Regresar al número
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