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Summary
Jun 2005, Vol. 1, No. 3, Pages 323-330
(doi:10.1517/14796694.1.3.323)

Single nucleotide polymorphism: a new risk factor for endometrial cancer?
Sokbom Kang, Ju Won Roh & Jae Weon Kim
Research Institute and Hospital, Center for Cervical Cancer, Research Institute and Hospital, National Cancer Center, Goyang, Gyeonggi, 411-764, Korea
Dongguk University, Department of Obstetrics and Gynecology, Dongguk University, Goyang, Gyeonggi, 411-773, Korea
Seoul National University, Department of Obstetrics and Gynecology, and, Cancer Research Institute, and, Human Genome Research Institute, 28 Yungun-Dong, Chongno-Ku, Seoul, 110-744, Korea.
† Author for correspondence



Continuous identification of common polymorphisms in various genes helps us to understand the possible association between endometrial cancer risk and the germline polymorphism. Estrogen receptor genes and the group of genes associated with the metabolism of estrogen have been investigated well. Second, the polymorphism in the p53 gene and the genes involved in its downstream pathway were correlated to a risk of developing endometrial cancer. Finally, the polymorphism in the genes involved in cellular proliferation and differentiation, regulating cell cycles, and DNA-damage repair were studied. In this way, recent research has begun to identify common genetic polymorphisms that augment the effects of risk-factor exposure, such as genes that affect the metabolism of hormones or are involved in cellular anti-tumor activities. The accumulation of data through these approaches would make genetic testing for the risk of development of endometrial cancer possible in the near future.

Cited by

Larissa A Meyer, Shannon N Westin, Karen H Lu, Michael R Milam. (2008) Genetic polymorphisms and endometrial cancer risk. Expert Review of Anticancer Therapy 8:7, 1159-1167
Online publication date: 1-Aug-2008.
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Authors:
Sokbom Kang
Ju Won Roh
Jae Weon Kim
Keywords:
endometrial cancer
estrogen
germline mutation
p53
polymorphism