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Identification of c-MYC as a target of the APC pathway
被引:4035
|作者:
He, TC
Sparks, AB
Rago, C
Hermeking, H
Zawel, L
da Costa, LT
Morin, PJ
Vogelstein, B
Kinzler, KW
机构:
[1] Johns Hopkins Oncol Ctr, Baltimore, MD 21231 USA
[2] Howard Hughes Med Inst, Baltimore, MD 21231 USA
[3] Johns Hopkins Univ, Sch Med, Program Human Genet, Baltimore, MD 21205 USA
[4] NIA, Baltimore, MD 21224 USA
来源:
关键词:
D O I:
10.1126/science.281.5382.1509
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
The adenomatous polyposis coil gene (APC) is a tumor suppressor gene that is inactivated in most colorectal cancers. Mutations of APC cause aberrant accumulation of beta-catenin, which then binds T cell factor-4 (Tcf-4), causing increased transcriptional activation of unknown genes. Here, the c-MYC oncogene is identified as a target gene in this signaling pathway. Expression of c-MYC was shown to be repressed by wild-type APC and activated by beta-catenin, and these effects were mediated through Tcf-4 binding sites in the c-MYC promoter. These results provide a molecular framework for understanding the previously enigmatic overexpression of c-MYC in colorectal cancers.
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页码:1509 / 1512
页数:4
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