Methylation silencing of ULK2, an autophagy gene, is essential for astrocyte transformation and tumor growth.

Autor:	Shukla S; From the Department of Microbiology and Cell Biology, Indian Institute of Science, Bangalore 560012, India., Patric IR; From the Department of Microbiology and Cell Biology, Indian Institute of Science, Bangalore 560012, India., Patil V; From the Department of Microbiology and Cell Biology, Indian Institute of Science, Bangalore 560012, India., Shwetha SD; Neuropathology, National Institute of Mental Health and Neuro Sciences, Bangalore 560029, India., Hegde AS; the Sri Satya Sai Institute of Higher Medical Sciences, Bangalore 560066, India, and., Chandramouli BA; the Departments of Neurosurgery and., Arivazhagan A; the Departments of Neurosurgery and., Santosh V; Neuropathology, National Institute of Mental Health and Neuro Sciences, Bangalore 560029, India., Somasundaram K; From the Department of Microbiology and Cell Biology, Indian Institute of Science, Bangalore 560012, India, skumar@mcbl.iisc.ernet.in.
Jazyk:	angličtina
Zdroj:	The Journal of biological chemistry [J Biol Chem] 2014 Aug 08; Vol. 289 (32), pp. 22306-18. Date of Electronic Publication: 2014 Jun 12.
DOI:	10.1074/jbc.M114.567032
Abstrakt:	Glioblastoma (GBM) is the most aggressive type of brain tumor and shows very poor prognosis. Here, using genome-wide methylation analysis, we show that G-CIMP+ and G-CIMP-subtypes enrich distinct classes of biological processes. One of the hypermethylated genes in GBM, ULK2, an upstream autophagy inducer, was found to be down-regulated in GBM. Promoter hypermethylation of ULK2 was confirmed by bisulfite sequencing. GBM and glioma cell lines had low levels of ULK2 transcripts, which could be reversed upon methylation inhibitor treatment. ULK2 promoter methylation and transcript levels showed significant negative correlation. Ectopic overexpression of ULK2-induced autophagy, which further enhanced upon nutrient starvation or temozolomide chemotherapy. ULK2 also inhibited the growth of glioma cells, which required autophagy induction as kinase mutant of ULK2 failed to induce autophagy and inhibit growth. Furthermore, ULK2 induced autophagy and inhibited growth in Ras-transformed immortalized Baby Mouse Kidney (iBMK) ATG5(+/+) but not in autophagy-deficient ATG5(-/-) cells. Growth inhibition due to ULK2 induced high levels of autophagy under starvation or chemotherapy utilized apoptotic cell death but not at low levels of autophagy. Growth inhibition by ULK2 also appears to involve catalase degradation and reactive oxygen species generation. ULK2 overexpression inhibited anchorage independent growth, inhibited astrocyte transformation in vitro and tumor growth in vivo. Of all autophagy genes, we found ULK2 and its homologue ULK1 were only down-regulated in all grades of glioma. Thus these results altogether suggest that inhibition of autophagy by ULK1/2 down-regulation is essential for glioma development. (© 2014 by The American Society for Biochemistry and Molecular Biology, Inc.)
Databáze:	MEDLINE
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