Tumor suppression by the Fbw7 ubiquitin ligase: mechanisms and opportunities.

Tumor suppression by the Fbw7 ubiquitin ligase: mechanisms and opportunities.
复制标题

DOI:
10.1016/j.ccell.2014.09.013
复制
发表时间:
2014-10-13
期刊:
影响因子:
50.3
通讯作者:
Clurman BE
Clurman BE
中科院分区:
医学1区
文献类型:
--
作者:
Davis RJ;Welcker M;Clurman BE

文献摘要

参考文献

被引文献

相似文献

肿瘤抑制因子对肿瘤发生具有广泛的影响,控制着广泛的致癌途径。蛋白质降解是一种新兴的机制,肿瘤抑制因子通过该机制调节多种途径,并以SCFFbw7泛素连接酶为例。快速积累的数据表明,SCFFbw7调节关键癌蛋白的网络。重要的是,编码Fbw7的FBXW7基因是人类癌症中最常见的突变基因之一。这些研究对肿瘤发生产生了重要的新见解,并可能很快实现针对Fbw7通路的治疗。在这里,我们专注于Fbw7在癌症中失调的机制和后果,并讨论可能的治疗方法。
Tumor suppressors with widespread impact on carcinogenesis control broad spectra of oncogenic pathways. Protein degradation is an emerging mechanism by which tumor suppressors regulate a diversity of pathways and is exemplified by the SCFFbw7 ubiquitin ligase. Rapidly accumulating data indicate that SCFFbw7 regulates a network of crucial oncoproteins. Importantly, the FBXW7 gene, which encodes Fbw7, is one of the most frequently mutated genes in human cancers. These studies are yielding important new insights into tumorigenesis and may soon enable therapies targeting the Fbw7 pathway. Here, we focus on the mechanisms and consequences of Fbw7 deregulation in cancers and discuss possible therapeutic approaches.
DOI: 10.1126/scisignal.2004088
发表时间: 2013-04-02
期刊: Science signaling
影响因子: 7.3
作者:
Gao J;Aksoy BA;Dogrusoz U;Dresdner G;Gross B;Sumer SO;Sun Y;Jacobsen A;Sinha R;Larsson E;Cerami E;Sander C;Schultz N
通讯作者: Schultz N
DOI: 10.1038/ncb2463
发表时间: 2012-03-04
影响因子: 21.3
作者:
通讯作者: --
DOI: 10.1038/nature12113
发表时间: 2013-05-02
期刊: Nature
影响因子: 64.8
作者:
通讯作者: --
DOI: 10.1084/jem.20100830
发表时间: 2011-02-14
期刊: The Journal of experimental medicine
影响因子: --
作者:
Babaei-Jadidi R;Li N;Saadeddin A;Spencer-Dene B;Jandke A;Muhammad B;Ibrahim EE;Muraleedharan R;Abuzinadah M;Davis H;Lewis A;Watson S;Behrens A;Tomlinson I;Nateri AS
通讯作者: Nateri AS
DOI: 10.1101/gad.10.16.1979
发表时间: 1996-08-15
影响因子: 10.5
作者:
Clurman, BE;Sheaff, RJ;Roberts, JM
通讯作者: Roberts, JM