TBK1 Kinase Addiction in Lung Cancer Cells Is Mediated via Autophagy of Tax1bp1/Ndp52 and Non-Canonical NF-[kappa]B Signalling

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-R...

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Veröffentlicht in:PloS one 2012-11, Vol.7 (11), p.e50672
Hauptverfasser: Newman, Alice C, Scholefield, Caroline L, Kemp, Alain J, Newman, Michelle, McIver, Edward G, Kamal, Ahmad, Wilkinson, Simon
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Sprache:eng
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Zusammenfassung: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.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0050672