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Inhibiting TRAF2-mediated Activation of NF-κB Facilitates Induction of AP-1
被引:29
|作者:
Manna, Sunil K.
[1
]
Babajan, Banaganapalli
[2
]
Raghavendra, Pongali B.
[1
,2
]
Raviprakash, Nune
[1
]
Sureshkumar, Chitta
[2
]
机构:
[1] Ctr DNA Fingerprinting & Diagnost, Immunol Lab, Hyderabad 500001, Andhra Pradesh, India
[2] Sri Krishnadevaraya Univ, Dept Biochem, Anantapur 515003, Andhra Pradesh, India
关键词:
C-JUN;
POTENTIATES APOPTOSIS;
RELA PHOSPHORYLATION;
PROTEIN;
MECHANISM;
CELLS;
TRADD-TRAF2;
PROGRESSION;
EXPRESSION;
ANTITUMOR;
D O I:
10.1074/jbc.M109.094961
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The compound 5-(4-methoxyarylimino)-2-N-(3,4-dichlorophenyl)3-oxo-1,2,4-thiadiazolidine (P-3-25) is known to possess anti-bacterial, anti-fungal, and anti-tubercular activities. In this report, we provide evidence that P-3-25 inhibits NF-kappa B, known to induce inflammatory and tumorigenic responses. It activates AP-1, another transcription factor. It inhibits TRAF2-mediated NF-kappa B activation but not TRAF6-mediated NF-kappa B DNA binding by preventing its association with TANK ( TRAF for NF-kappa B). It facilitates binding of MEKK1 with TRAF2 and thereby activates JNK and AP-1. We provide evidence, for the first time, that suggests that the interaction of P3-25 with TRAF2 leads to inhibition of the NF-kappa B pathway and activation of AP-1 pathway. These results suggest novel approaches to design of P3-25 as an anti-cancer/inflammatory drug for therapy through regulation of the TRAF2 pathway.
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页码:11617 / 11627
页数:11
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