Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/107313
Citations
Scopus Web of Science® Altmetric
?
?
Type: Journal article
Title: Mutant p53 upregulates alpha-1 antitrypsin expression and promotes invasion in lung cancer
Author: Shakya, R.
Tarulli, G.
Sheng, L.
Lokman, N.
Ricciardelli, C.
Pishas, K.
Selinger, C.
Kohonen-Corish, M.
Cooper, W.
Turner, A.
Neilsen, P.
Callen, D.
Citation: Oncogene, 2017; 36(31):4469-4480
Publisher: Nature Publishing Group
Issue Date: 2017
ISSN: 0950-9232
1476-5594
Statement of
Responsibility: 
R Shakya, GA Tarulli, L Sheng, NA Lokman, C Ricciardelli, KI Pishas, CI Selinger, MRJ Kohonen-Corish, WA Cooper, AG Turner, PM Neilsen and DF Callen
Abstract: Missense mutations in the TP53 tumor-suppressor gene inactivate its antitumorigenic properties and endow the incipient cells with newly acquired oncogenic properties that drive invasion and metastasis. Although the oncogenic effect of mutant p53 transcriptome has been widely acknowledged, the global influence of mutant p53 on cancer cell proteome remains to be fully elucidated. Here, we show that mutant p53 drives the release of invasive extracellular factors (the 'secretome') that facilitates the invasion of lung cancer cell lines. Proteomic characterization of the secretome from mutant p53-inducible H1299 human non-small cell lung cancer cell line discovered that the mutant p53 drives its oncogenic pathways through modulating the gene expression of numerous targets that are subsequently secreted from the cells. Of these genes, alpha-1 antitrypsin (A1AT) was identified as a critical effector of mutant p53 that drives invasion in vitro and in vivo, together with induction of epithelial-mesenchymal transition markers expression. Mutant p53 upregulated A1AT transcriptionally through the involvement with its family member p63. Conditioned medium containing secreted A1AT enhanced cell invasion, while an A1AT-blocking antibody attenuated the mutant p53-driven migration and invasion. Importantly, high A1AT expression correlated with increased tumor stage, elevated p53 staining and shorter overall survival in lung adenocarcinoma patients. Collectively, these findings suggest that A1AT is an indispensable target of mutant p53 with prognostic and therapeutic potential in mutant p53-expressing tumors.
Keywords: Cell Line, Tumor
Humans
Lung Neoplasms
Neoplasm Invasiveness
alpha 1-Antitrypsin
Proteomics
Cell Cycle
Cell Movement
Up-Regulation
Mutation
Tumor Suppressor Protein p53
Epithelial-Mesenchymal Transition
Description: Published online 3 April 2017
Rights: © 2017 Macmillan Publishers Limited, part of Springer Nature. All rights reserved.
DOI: 10.1038/onc.2017.66
Grant ID: http://purl.org/au-research/grants/nhmrc/44107714
http://purl.org/au-research/grants/nhmrc/44112162
Appears in Collections:Aurora harvest 3
Medicine publications

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.