Small molecule blockade of transcriptional coactivation of the hypoxia-inducible factor pathway

被引:527
作者
Kung, AL [1 ]
Zabludoff, SD
France, DS
Freedman, SJ
Tanner, EA
Vieira, A
Cornell-Kennon, S
Lee, J
Wang, BQ
Wang, JM
Memmert, K
Naegeli, HU
Petersen, F
Eck, MJ
Bair, KW
Wood, AW
Livingston, DM
机构
[1] Harvard Univ, Sch Med, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Boston, MA 02115 USA
[3] Dana Farber Canc Inst, Dept Pediat Oncol, Boston, MA 02115 USA
[4] Childrens Hosp, Boston, MA 02115 USA
[5] Novartis Pharmaceut, Dept Oncol, Cambridge, MA 02139 USA
[6] Beth Israel Deaconess Med Ctr, Div Hematol Oncol, Boston, MA 02115 USA
[7] Novartis Pharma AG Nat Prod Unit, Discovery Technol, CH-4002 Basel, Switzerland
关键词
D O I
10.1016/j.ccr.2004.06.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Homeostasis under hypoxic conditions is maintained through a coordinated transcriptional response mediated by the hypoxia-inducible factor (HIF) pathway and requires coactivation by the CBP and p300 transcriptional coactivators. Through a target-based high-throughput screen, we identified chetomin as a disrupter of HIF binding to p300. At a molecular level, chetomin disrupts the structure of the CH1 domain of p300 and precludes its interaction with HIF, thereby attenuating hypoxia-inducible transcription. Systemic administration of chetomin inhibited hypoxia-inducible transcription within tumors and inhibited tumor growth. These results demonstrate a therapeutic window for pharmacological attenuation of HIF activity and further establish the feasibility of disrupting a signal transduction pathway by targeting the function of a transcriptional coactivator with a small molecule.
引用
收藏
页码:33 / 43
页数:11
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