A microRNA component of the p53 tumour suppressor network

被引:0
|
作者
Lin He
Xingyue He
Lee P. Lim
Elisa de Stanchina
Zhenyu Xuan
Yu Liang
Wen Xue
Lars Zender
Jill Magnus
Dana Ridzon
Aimee L. Jackson
Peter S. Linsley
Caifu Chen
Scott W. Lowe
Michele A. Cleary
Gregory J. Hannon
机构
[1] Watson School of Biological Sciences,
[2] Howard Hughes Medical Institute,undefined
[3] Cold Spring Harbor Laboratory,undefined
[4] 1 Bungtown Road,undefined
[5] Cold Spring Harbor,undefined
[6] New York 11724,undefined
[7] USA,undefined
[8] Program in Genetics,undefined
[9] Stony Brook University,undefined
[10] Stony Brook,undefined
[11] New York 11794,undefined
[12] USA,undefined
[13] Rosetta Inpharmatics,undefined
[14] 401 Terry Avenue N.,undefined
[15] Seattle,undefined
[16] Washington 98109,undefined
[17] USA,undefined
[18] Advanced Research & Technology,undefined
[19] Applied Biosystems,undefined
[20] 850 Lincoln Centre Drive,undefined
[21] Foster City,undefined
[22] California 94404,undefined
[23] USA,undefined
[24] Present address: Memorial Sloan-Kettering Cancer Center,undefined
[25] 415 East 68th Street,undefined
[26] New York,undefined
[27] New York 10021,undefined
[28] USA.,undefined
来源
Nature | 2007年 / 447卷
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摘要
The tumour suppressor p53 is the most commonly mutated gene in human cancers, and probably nearly all tumours have a lesion somewhere in this pathway. The p53 network is activated in response to numerous insults to restrain inappropriate cell proliferation either via growth arrest or cell death. MicroRNAs (miRNAs) are increasingly recognized for playing important parts in cancer, but little is know about how miRNA expression is regulated. Now a miRNA component of the p53 tumour suppressor network has been identified: p53 directly activates the transcription of the miR-34 family of miRNAs, which themselves suppress cell proliferation. Though dozens of p53 targets are known in mammals, miR-34 is unusual in that it is also present in Drosophila and the nematode worm C. elegans. This suggests that the link between p53 and miR-34 may have arisen early in the evolution of the p53 network.
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页码:1130 / 1134
页数:4
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