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
引用
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页数:12
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