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TBK1 Kinase Addiction in Lung Cancer Cells Is Mediated via Autophagy of Tax1bp1/Ndp52 and Non-Canonical NF-κB Signalling
被引:100
|作者:
Newman, Alice C.
[1
]
Scholefield, Caroline L.
[1
]
Kemp, Alain J.
[1
]
Newman, Michelle
[2
]
McIver, Edward G.
[2
]
Kamal, Ahmad
[2
]
Wilkinson, Simon
[1
]
机构:
[1] Univ Edinburgh, MRC Inst Genet & Mol Med, Edinburgh Canc Res UK Ctr, Edinburgh, Midlothian, Scotland
[2] MRC Technol, Ctr Therapeut Discovery, London, England
来源:
PLOS ONE
|
2012年
/
7卷
/
11期
关键词:
ACTIVATION;
PHOSPHORYLATION;
TUMORIGENESIS;
SURVIVAL;
PROTEIN;
TANK;
PROLIFERATION;
REQUIREMENT;
MATURATION;
RESTRICTS;
D O I:
10.1371/journal.pone.0050672
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
K-Ras dependent non-small cell lung cancer (NSCLC) cells are 'addicted' to basal autophagy that reprograms cellular metabolism in a lysosomal-sensitive manner. Here we demonstrate that the xenophagy-associated kinase TBK1 drives basal autophagy, consistent with its known requirement in K-Ras-dependent NSCLC proliferation. Furthermore, basal autophagy in this context is characterised by sequestration of the xenophagy cargo receptor Ndp52 and its paralogue Tax1bp1, which we demonstrate here to be a bona fide cargo receptor. Autophagy of these cargo receptors promotes non-canonical NF-kappa B signalling. We propose that this TBK1-dependent mechanism for NF-kappa B signalling contributes to autophagy addiction in K-Ras driven NSCLC. Citation: Newman AC, Scholefield CL, Kemp AJ, Newman M, McIver EG, et al. (2012) TBK1 Kinase Addiction in Lung Cancer Cells Is Mediated via Autophagy of Tax1bp1/Ndp52 and Non-Canonical NF-kappa B Signalling. PLoS ONE 7(11): e50672. doi: 10.1371/journal.pone.0050672
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页数:12
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