Coupling of glucose deprivation with impaired histone H2B monoubiquitination in tumors.

Metabolic reprogramming is associated with tumorigenesis. However, glucose metabolism in tumors is poorly understood. Here, we report that glucose levels are significantly lower in bulk tumor specimens than those in normal tissues of the same tissue origins. We show that mono-ubiquitinated histone H...

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Main Authors: Yasuyo Urasaki, Linda Heath, C Wilson Xu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3353945?pdf=render
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author Yasuyo Urasaki
Linda Heath
C Wilson Xu
author_facet Yasuyo Urasaki
Linda Heath
C Wilson Xu
author_sort Yasuyo Urasaki
collection DOAJ
description Metabolic reprogramming is associated with tumorigenesis. However, glucose metabolism in tumors is poorly understood. Here, we report that glucose levels are significantly lower in bulk tumor specimens than those in normal tissues of the same tissue origins. We show that mono-ubiquitinated histone H2B (uH2B) is a semi-quantitative histone marker for glucose. We further show that loss of uH2B occurs specifically in cancer cells from a wide array of tumor specimens of breast, colon, lung and additional 23 anatomic sites. In contrast, uH2B levels remain high in stromal tissues or non-cancerous cells in the tumor specimens. Taken together, our data suggest that glucose deficiency and loss of uH2B are novel properties of cancer cells in vivo, which may represent important regulatory mechanisms of tumorigenesis.
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spelling doaj.art-35c86bfdf25b41e3b1929144a135e97c2022-12-22T00:35:19ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0175e3677510.1371/journal.pone.0036775Coupling of glucose deprivation with impaired histone H2B monoubiquitination in tumors.Yasuyo UrasakiLinda HeathC Wilson XuMetabolic reprogramming is associated with tumorigenesis. However, glucose metabolism in tumors is poorly understood. Here, we report that glucose levels are significantly lower in bulk tumor specimens than those in normal tissues of the same tissue origins. We show that mono-ubiquitinated histone H2B (uH2B) is a semi-quantitative histone marker for glucose. We further show that loss of uH2B occurs specifically in cancer cells from a wide array of tumor specimens of breast, colon, lung and additional 23 anatomic sites. In contrast, uH2B levels remain high in stromal tissues or non-cancerous cells in the tumor specimens. Taken together, our data suggest that glucose deficiency and loss of uH2B are novel properties of cancer cells in vivo, which may represent important regulatory mechanisms of tumorigenesis.http://europepmc.org/articles/PMC3353945?pdf=render
spellingShingle Yasuyo Urasaki
Linda Heath
C Wilson Xu
Coupling of glucose deprivation with impaired histone H2B monoubiquitination in tumors.
PLoS ONE
title Coupling of glucose deprivation with impaired histone H2B monoubiquitination in tumors.
title_full Coupling of glucose deprivation with impaired histone H2B monoubiquitination in tumors.
title_fullStr Coupling of glucose deprivation with impaired histone H2B monoubiquitination in tumors.
title_full_unstemmed Coupling of glucose deprivation with impaired histone H2B monoubiquitination in tumors.
title_short Coupling of glucose deprivation with impaired histone H2B monoubiquitination in tumors.
title_sort coupling of glucose deprivation with impaired histone h2b monoubiquitination in tumors
url http://europepmc.org/articles/PMC3353945?pdf=render
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AT cwilsonxu couplingofglucosedeprivationwithimpairedhistoneh2bmonoubiquitinationintumors