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Data · dataset · 2023

ATF4-dependent fructolysis fuels growth of glioblastoma multiforme

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Excessive consumption of fructose in the Western diet contributes to cancer development.

Description

However, it is still unclear how cancer cells coordinate glucose and fructose metabolism during tumor malignant progression. We demonstrate here that glioblastoma multiforme (GBM) cells switch their energy supply from glycolysis to fructolysis in response to glucose deprivation.

Mechanistically, glucose deprivation induces expression of two essential fructolytic proteins GLUT5 and ALDOB through selectively activating translation of activating transcription factor 4 (ATF4). Functionally, genetic or pharmacological disruption of ATF4-dependent fructolysis significantly inhibits growth and colony formation of GBM cells in vitro and GBM growth in vivo. In addition, ATF4, GLUT5, and ALDOB levels positively correlate with each other in GBM specimens and are poor prognostic indicators in GBM patients.

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This work highlights ATF4-dependent fructolysis as a metabolic feature and a potential therapeutic target for GBM.

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Catalogue records · 1

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Inferred from text
Biochemistry and cell biology 72% · Cancer 75%
Provenance · 1 source records, 13 field assertions
SourceKeyLast seenRaw
ScienceDB10.57760/sciencedb.073509 d agoJSON v1
FieldAssertionExtractorEvidence
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