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[Cancer Research 60, 4328-4330, August 15, 2000]
© 2000 American Association for Cancer Research


Advances in Brief

Mutations of the bak Gene in Human Gastric and Colorectal Cancers

Shinya Kondo1, Yasuhisa Shinomura, Yoshiji Miyazaki, Tatsuya Kiyohara, Shusaku Tsutsui, Shinji Kitamura, Yutaka Nagasawa, Masanori Nakahara, Shuji Kanayama and Yuji Matsuzawa

Department of Internal Medicine and Molecular Science, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan [S. Ko., Y. S., Y. Mi., T. K., S. T., S. Ki., Y. N., M. N., Y. Ma.], and Department of Gastroenterology, Sumitomo Hospital, Osaka 530-0005, Japan [S. Ko., S. Ka.]

The Bcl-2 homologue Bak is a potent inducer of apoptosis. We performed PCR-based single-strand conformational polymorphism and sequencing analysis of the entire coding region of the bak gene (exons 2–6) in 24 primary gastric cancers (6 early-stage and 18 advanced-stage cancers) and 20 primary colorectal cancers (6 early-stage and 14 advanced-stage cancers). The data herein demonstrate, for the first time, the mutation of the bak gene in gastric and colorectal cancers. Missense bak gene mutations were observed in 3 of 24 (12.5%) gastric cancers and 2 of 20 (10.0%) colorectal cancers. Sequence alterations without amino acid alteration were observed 1 of 24 (4.2%) gastric cancers and 2 of 20 (10.0%) colorectal cancers. Mutations in the bak gene were observed only in advanced-stage gastrointestinal cancers but not in early-stage cancers. Our observations suggest that mutations in this gene predispose bearers to the development of gastrointestinal malignancies in at least a subset of the cases.




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