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Volume 45, Issue 12, Pages 1032-1036 (December 2009)


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Detection of copy number amplification of cyclin D1 (CCND1) and cortactin (CTTN) in oral carcinoma and oral brushed samples from areca chewers

Hui-Shen Liua1, Hsuan-Hsuan Lua1, Mann-Tin Luiab, En-Hao Yuac, Wilma Shena, Yu-Ping Chena, Kuo-Wei Changa, Hsi-Feng TuacCorresponding Author Informationemail addressemail address

Received 6 June 2009; received in revised form 24 June 2009; accepted 25 June 2009. published online 10 August 2009.

Summary 

Oral squamous cell carcinoma (OSCC) in Asians is highly associated with the abuse of areca (betel) chewing. There are several hundred million Asians who chew areca and are therefore at high risk of OSCC. Aberrance in cyclin D1 (CCND1) and/or cortactin (CTTN), which are localized on 11q13, seems to be critical events for the development of oral carcinogenesis. This study identified amplifications of CCND1 and CTTN by quantitative (Q)-PCR analysis in 50% and 45% of OSCC samples, respectively. Co-amplification of both genes was identified in 20% of tumors. Higher CTTN expression was associated with nodal metastasis of the OSCC, while the amplification of CCND1 was identified in 28% of oral brushed samples from areca chewers, who form a high risk group for OSCC. This study confirms the importance of alterations in CCND1 and CTTN with respect to areca-associated OSCC, and demonstrates that there is an early occurrence of amplification of these genes in the risk population. The non-invasive brushing sampling method coupling with Q-PCR analysis needs to be validated for use as an early detection system for gene copy changes, which should aid oral cancer prevention.

a School of Dentistry, National Yang-Ming University, Taipei, Taiwan

b Department of Dentistry, Veterans General Hospital, Taipei, Taiwan

c Department of Dentistry, National Yang-Ming University Hospital, I-Lan, Taiwan

Corresponding Author InformationCorresponding author. Address: No. 152, Xin Min Road, I-Lan, Taiwan 260, Taiwan. Tel.: +886 93 7546801; fax: +886 3 9351838.

1 Equal contribution to this work.

PII: S1368-8375(09)00826-4

doi:10.1016/j.oraloncology.2009.06.007


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