Autor: |
Newman AC; Edinburgh Cancer Research UK Centre, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom., Scholefield CL, Kemp AJ, Newman M, McIver EG, Kamal A, Wilkinson S |
Jazyk: |
angličtina |
Zdroj: |
PloS one [PLoS One] 2012; Vol. 7 (11), pp. e50672. Date of Electronic Publication: 2012 Nov 29. |
DOI: |
10.1371/journal.pone.0050672 |
Abstrakt: |
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-κB signalling. We propose that this TBK1-dependent mechanism for NF-κB signalling contributes to autophagy addiction in K-Ras driven NSCLC. |
Databáze: |
MEDLINE |
Externí odkaz: |
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