CJO - Abstract - Nasopharyngeal carcinoma: molecular pathogenesis and therapeutic developments

Cambridge Journals Online

Cambridge Journals Online
Expert Reviews in Molecular Medicine (2007), 9 : 1-24 Cambridge University Press
Copyright © 2007 Cambridge University Press
doi:10.1017/S1462399407000312 (About doi)
Published online by Cambridge University Press 04 May 2007
Expert Reviews in Molecular Medicine (2007), 9:12:1-24 Cambridge University Press
Copyright © 2007 Cambridge University Press
doi:10.1017/S1462399407000312

Review Article

Nasopharyngeal carcinoma: molecular pathogenesis and therapeutic developments


Qian Tao a1c1 and Anthony T.C. Chan a1c1
a1 Cancer Epigenetics Laboratory, State Key Laboratory in Oncology in South China, Sir YK Pao Centre for Cancer, Department of Clinical Oncology, Hong Kong Cancer Institute and Li Ka Shing Institute of Health Sciences, Chinese University of Hong Kong.

Article author query
tao q   Google Scholar 
chan at   Google Scholar 
 

Abstract

Nasopharyngeal carcinoma (NPC) is a prevalent tumour in southern China and southeast Asia, particularly in the Cantonese population, where its incidence has remained high for decades. Recent studies have demonstrated that the aetiology of NPC is complex, involving multiple factors including genetic susceptibility, infection with the Epstein–Barr virus (EBV) and exposure to chemical carcinogens. During development of the disease, viral infection and multiple somatic genetic and epigenetic changes synergistically disrupt normal cell function, thus contributing to NPC pathogenesis. NPC is highly radiosensitive and chemosensitive, but treatment of patients with locoregionally advanced disease remains problematic. New biomarkers for NPC, including EBV DNA copy number or methylation of multiple tumour suppressor genes, which can be detected in serum and nasopharyngeal brushings, have been developed for the molecular diagnosis of this tumour. Meanwhile, new therapeutic strategies such as intensity-modulated radiation therapy and immuno- and epigenetic therapies might lead to more specific and effective treatments.


Correspondence:
c1 Corresponding authors: Qian Tao, Rm 315, Cancer Center, PWH, Chinese University of Hong Kong, Shatin, Hong Kong. Tel:  +852 2632 1340; Fax:  +852 2648 8842; E-mail: qtao@clo.cuhk.edu.hk
c2 Anthony T.C. Chan, Department of Clinical Oncology, Chinese University of Hong Kong, Shatin, Hong Kong. Tel:  +852 2632 2119; Fax:  +852 2649 7426; E-mail: anthonytcchan@cuhk.edu.hk.


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