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Glutamate and asparagine cataplerosis underlie glutamine addiction in melanoma

Glutamine dependence is a prominent feature of cancer metabolism, and here we show that melanoma cells, irrespective of their oncogenic background, depend on glutamine for growth. A quantitative audit of how carbon from glutamine is used showed that TCA-cycle-derived glutamate is, in most melanoma c...

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Autores principales: Ratnikov, Boris, Aza-Blanc, Pedro, Ronai, Ze'ev A., Smith, Jeffrey W., Osterman, Andrei L., Scott, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4480687/
https://www.ncbi.nlm.nih.gov/pubmed/25749035
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author Ratnikov, Boris
Aza-Blanc, Pedro
Ronai, Ze'ev A.
Smith, Jeffrey W.
Osterman, Andrei L.
Scott, David A.
author_facet Ratnikov, Boris
Aza-Blanc, Pedro
Ronai, Ze'ev A.
Smith, Jeffrey W.
Osterman, Andrei L.
Scott, David A.
author_sort Ratnikov, Boris
collection PubMed
description Glutamine dependence is a prominent feature of cancer metabolism, and here we show that melanoma cells, irrespective of their oncogenic background, depend on glutamine for growth. A quantitative audit of how carbon from glutamine is used showed that TCA-cycle-derived glutamate is, in most melanoma cells, the major glutamine-derived cataplerotic output and product of glutaminolysis. In the absence of glutamine, TCA cycle metabolites were liable to depletion through aminotransferase-mediated α-ketoglutarate-to-glutamate conversion and glutamate secretion. Aspartate was an essential cataplerotic output, as melanoma cells demonstrated a limited capacity to salvage external aspartate. Also, the absence of asparagine increased the glutamine requirement, pointing to vulnerability in the aspartate-asparagine biosynthetic pathway within melanoma metabolism. In contrast to melanoma cells, melanocytes could grow in the absence of glutamine. Melanocytes use more glutamine for protein synthesis rather than secreting it as glutamate and are less prone to loss of glutamate and TCA cycle metabolites when starved of glutamine.
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spelling pubmed-44806872015-06-26 Glutamate and asparagine cataplerosis underlie glutamine addiction in melanoma Ratnikov, Boris Aza-Blanc, Pedro Ronai, Ze'ev A. Smith, Jeffrey W. Osterman, Andrei L. Scott, David A. Oncotarget Priority Research Paper Glutamine dependence is a prominent feature of cancer metabolism, and here we show that melanoma cells, irrespective of their oncogenic background, depend on glutamine for growth. A quantitative audit of how carbon from glutamine is used showed that TCA-cycle-derived glutamate is, in most melanoma cells, the major glutamine-derived cataplerotic output and product of glutaminolysis. In the absence of glutamine, TCA cycle metabolites were liable to depletion through aminotransferase-mediated α-ketoglutarate-to-glutamate conversion and glutamate secretion. Aspartate was an essential cataplerotic output, as melanoma cells demonstrated a limited capacity to salvage external aspartate. Also, the absence of asparagine increased the glutamine requirement, pointing to vulnerability in the aspartate-asparagine biosynthetic pathway within melanoma metabolism. In contrast to melanoma cells, melanocytes could grow in the absence of glutamine. Melanocytes use more glutamine for protein synthesis rather than secreting it as glutamate and are less prone to loss of glutamate and TCA cycle metabolites when starved of glutamine. Impact Journals LLC 2015-02-28 /pmc/articles/PMC4480687/ /pubmed/25749035 Text en Copyright: © 2015 Ratnikov et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Priority Research Paper
Ratnikov, Boris
Aza-Blanc, Pedro
Ronai, Ze'ev A.
Smith, Jeffrey W.
Osterman, Andrei L.
Scott, David A.
Glutamate and asparagine cataplerosis underlie glutamine addiction in melanoma
title Glutamate and asparagine cataplerosis underlie glutamine addiction in melanoma
title_full Glutamate and asparagine cataplerosis underlie glutamine addiction in melanoma
title_fullStr Glutamate and asparagine cataplerosis underlie glutamine addiction in melanoma
title_full_unstemmed Glutamate and asparagine cataplerosis underlie glutamine addiction in melanoma
title_short Glutamate and asparagine cataplerosis underlie glutamine addiction in melanoma
title_sort glutamate and asparagine cataplerosis underlie glutamine addiction in melanoma
topic Priority Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4480687/
https://www.ncbi.nlm.nih.gov/pubmed/25749035
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