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Carcinogenesis Advance Access published online on July 17, 2007
Carcinogenesis, doi:10.1093/carcin/bgm168
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© The Author 2007. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Interaction of P53 Arg72Pro and MDM2 T309G polymorphisms and their associations with risk of gastric cardia cancer

Ming Yang1,{dagger}, Yongli Guo1,{dagger}, Xuemei Zhang1, Xiaoping Miao1, Wen Tan1, Tong Sun1, Dan Zhao1, Dianke Yu1, Junniao Liu1 and Dongxin Lin1,*

1 Department of Etiology & Carcinogenesis, Cancer Institute, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China

* To whom correspondence should be addressed: Tel: 86-10-87788491; Fax: 86-10-67722460; E-mail: dlin{at}public.bta.net.cn

The P53 tumor suppressor pathway plays an important role in cancer development. The auto-regulatory feedback mechanism of the P53 and MDM2 expression is critical in keeping proper tumor suppressor function of this pathway. This study examined the effect of P53 Arg72Pro variants on transactivation of polymorphic MDM2 promoter (T309G) and their associations with risk of developing gastric cardia adenocarcinoma (GCA) in a Chinese population. Luciferase assays consistently showed a significantly higher activity of the MDM2 309G promoter compared with the MDM2 309T promoter. In cells cotransfected with variant P53 cDNAs, P53-72Pro displayed a significantly higher ability to activate the MDM2 promoter than P53-72Arg. Genotype analyses in 500 GCA patients and 1000 controls showed that significantly increased risk for developing GCA was associated with the MDM2 309G and the P53 72Pro allele compared with the MDM2 309T and the P53 72Arg allele in an allele-dose dependent manner. A joint effect between the MDM2 and P53 polymorphisms in intensifying GCA risk was detected, with the OR for the presence of both MDM2 390GG and P53 72Pro/Pro genotypes being 5.05 (95% CI, 2.50–10.20). These results suggest that the P53 72Pro and MDM2 309G polymorphisms contribute to the risk of developing GCA.

Key Words: MDM2 • P53 • polymorphism • gastric cardia cancer

{dagger} These authors contribute equally to this work.

Received May 23, 2007; revised July 1, 2007; accepted July 12, 2007.


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