4.8 Article

Regional glutamine deficiency in tumours promotes dedifferentiation through inhibition of histone demethylation

Journal

NATURE CELL BIOLOGY
Volume 18, Issue 10, Pages 1090-1101

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/ncb3410

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Funding

  1. National Institutes of Health (NIH)/National Cancer Institute (NCI) [R01CA183989]
  2. Caltech-City of Hope Biomedical Initiative Pilot Grant
  3. American Cancer Society [RSG-16-085-01-TBE]
  4. Stand up to Cancer Philip A. Sharp Innovation in Collaboration Award
  5. DNA Damage Response and Oncogenic Signaling (DDROS) Training Program at City of Hope
  6. NIH/NCI [P30CA33572]

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Poorly organized tumour vasculature often results in areas of limited nutrient supply and hypoxia. Despite our understanding of solid tumour responses to hypoxia, how nutrient deprivation regionally affects tumour growth and therapeutic response is poorly understood. Here, we show that the core region of solid tumours displayed glutamine deficiency compared with other amino acids. Low glutamine in tumour core regions led to dramatic histone hypermethylation due to decreased alpha-ketoglutarate levels, a key cofactor for the Jumonji-domain-containing histone demethylases. Using patient-derived (V600E)BRAF melanoma cells, we found that low-glutamine-induced histone hypermethylation resulted in cancer cell dedifferentiation and resistance to BRAF inhibitor treatment, which was largely mediated by methylation on H3K27, as knockdown of the H3K27-specific demethylase KDM6B and the methyltransferase EZH2 respectively reproduced and attenuated the low-glutamine effects in vitro and in vivo. Thus, intratumoral regional variation in the nutritional microenvironment contributes to tumour heterogeneity and therapeutic response.

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