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Essential role of tuberous sclerosis genes TSC1 and TSC2 in NF-κB activation and cell survival
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作者:

Ghosh, Sourav
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机构: Salk Inst Biol Studies, Mol & Cell Biol Lab, La Jolla, CA 92037 USA

Tergaonkar, Vinay
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h-index: 0
机构: Salk Inst Biol Studies, Mol & Cell Biol Lab, La Jolla, CA 92037 USA

Rothlin, Carla V.
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机构: Salk Inst Biol Studies, Mol & Cell Biol Lab, La Jolla, CA 92037 USA

Correa, Ricardo G.
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机构: Salk Inst Biol Studies, Mol & Cell Biol Lab, La Jolla, CA 92037 USA

Bottero, Virginie
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h-index: 0
机构: Salk Inst Biol Studies, Mol & Cell Biol Lab, La Jolla, CA 92037 USA

Bist, Pradeep
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机构: Salk Inst Biol Studies, Mol & Cell Biol Lab, La Jolla, CA 92037 USA

Verma, Inder M.
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机构: Salk Inst Biol Studies, Mol & Cell Biol Lab, La Jolla, CA 92037 USA

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机构:
[1] Salk Inst Biol Studies, Mol & Cell Biol Lab, La Jolla, CA 92037 USA
[2] Salk Inst Biol Studies, Genet Lab, La Jolla, CA 92037 USA
[3] Salk Inst Biol Studies, Mol Neurobiol Lab, La Jolla, CA 92037 USA
[4] Inst Mol & Cell Biol, Singapore 138673, Singapore
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D O I:
10.1016/j.ccr.2006.08.007
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
The TSCI-TSC2 complex has recently been implicated in cell survival responses. We observed that NF-kappa B signaling is attenuated in TSC1- and TSC2-deficient MEFs concomitant with reduced survival following DNA damage or TNFa alpha stimulation. Reconstitution of TSC2 expression in TSC2(-/-) MEFs rescued survival in an NF-kappa B activity-dependent manner. Furthermore, in TSC2(-/-) MEFs, the rapamycin-mediated inhibition of deregulated mTOR activity restored NF-kappa B activation and survival. This rapamycin-mediated effect was reversed by inhibition of NF-kappa B transcriptional activation or by inhibition of ERK1/2 MAP kinase or PI-3K pathways, which lie on signaling cascades that lead to NF-kappa B activation. These results provide evidence for a crosstalk between the TSC/Rheb/mTOR pathway and the NF-kappa B induction pathways and indicate that NF-kappa B functions as an important survival factor that regulates TSC2-dependent cell survival.
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页码:215 / 226
页数:12
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