Oncotarget

Research Papers:

Autophagy gene expression profiling identifies a defective microtubule-associated protein light chain 3A mutant in cancer

Joana R. Costa _, Krisna Prak, Sarah Aldous, Christina Anja Gewinner and Robin Ketteler

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Oncotarget. 2016; 7:41203-41216. https://doi.org/10.18632/oncotarget.9754

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Abstract

Joana R. Costa1, Krisna Prak1, Sarah Aldous1, Christina Anja Gewinner2 and Robin Ketteler1

1 MRC Laboratory for Molecular Cell Biology, University College London, London, United Kingdom

2 Translational Research Office, University College London, London, United Kingdom

Correspondence to:

Robin Ketteler, email:

Keywords: ATG4B, autophagy, gene expression, luciferase release assay, MAP1LC3A R70H

Received: May 11, 2016 Accepted: May 23, 2016 Published: May 31, 2016

Abstract

The cellular stress response autophagy has been implicated in various diseases including neuro-degeneration and cancer. The role of autophagy in cancer is not clearly understood and both tumour promoting and tumour suppressive effects of autophagy have been reported, which complicates the design of therapeutic strategies based on targeting the autophagy pathway. Here, we have systematically analyzed gene expression data for 47 autophagy genes for deletions, amplifications and mutations in various cancers. We found that several cancer types have frequent autophagy gene amplifications, whereas deletions are more frequent in prostate adenocarcinomas. Other cancer types such as glioblastoma and thyroid carcinoma show very few alterations in any of the 47 autophagy genes. Overall, individual autophagy core genes are altered at low frequency in cancer, suggesting that cancer cells require functional autophagy. Some autophagy genes show frequent single base mutations, such as members of the ULK family of protein kinases. Furthermore, we found hotspot mutations in the arginine-rich stretch in MAP1LC3A resulting in reduced cleavage of MAP1LC3A by ATG4B both in vitro and in vivo, suggesting a functional implication of this gene mutation in cancer development.


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PII: 9754