The pivotal role of endoplasmic reticulum in cancer glucose metabolism

The endoplasmic reticulum (ER) supports essential biosynthetic and quality control functions. These processes rely on sustained energy supply and precise redox control within the ER lumen. While ATP can be imported from mitochondria, pyridine nucleotides are impermeable to the ER membrane, necessitating compartment-specific mechanisms to regulate NAD(H) and NADP(H) pools. Here, we demonstrate that the ER-confined pentose phosphate pathway (ER-PPP), driven by hexose-6-phosphate dehydrogenase (H6PD), processes large amounts of glucose equivalents to preserve the local redox homeostasis in triple-negative breast cancer (TNBC) cells. <i>H6PD</i> silencing decreases the NADPH regeneration within the ER lumen. The consequent impairment of protein folding machinery accelerates lysosomes generation, up to disrupt the equivalence between the cell release of lactate and H<sup>+</sup>. Finally, the simultaneous impairment of glucose-6P (G6P) degradation (by <i>H6PD</i> silencing) and hydrolysis (by silencing glucose-6-phosphatase) eventually results in a measurable ER collapse documenting the high-rate nature of G6P flux across the reticular membrane.

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Publication Details

Journal
iScience
Published
2025-12-19
DOI
https://doi.org/10.1016/j.isci.2025.114503
Primary Topic
Endoplasmic Reticulum Stress and Disease
Type
article
Field-Weighted Citation Impact
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article

The pivotal role of endoplasmic reticulum in cancer glucose metabolism

Anna Maria Orengo, Andrea Benzi, Sabrina Chiesa, Santina Bruzzone et al.
iScience
Endoplasmic Reticulum Stress and Disease
article

The pivotal role of endoplasmic reticulum in cancer glucose metabolism

Anna Maria Orengo, Andrea Benzi, Sabrina Chiesa, Santina Bruzzone, Sonia Carta, Gianmario Sambuceti, Isotta Cainero, Matteo Bauckneht, Tiziana Bachetti, Gabriele Tancreda, Francesca Vitale, Maddalena Ghelardoni, Roberto Benelli, Silvia Bruno, Marco Scotto, Serena Losacco, Cecilia Marini, Margherita Raineri, Silvia Ravera
article en

Abstract

The endoplasmic reticulum (ER) supports essential biosynthetic and quality control functions. These processes rely on sustained energy supply and precise redox control within the ER lumen. While ATP can be imported from mitochondria, pyridine nucleotides are impermeable to the ER membrane, necessitating compartment-specific mechanisms to regulate NAD(H) and NADP(H) pools. Here, we demonstrate that the ER-confined pentose phosphate pathway (ER-PPP), driven by hexose-6-phosphate dehydrogenase (H6PD), processes large amounts of glucose equivalents to preserve the local redox homeostasis in triple-negative breast cancer (TNBC) cells. <i>H6PD</i> silencing decreases the NADPH regeneration within the ER lumen. The consequent impairment of protein folding machinery accelerates lysosomes generation, up to disrupt the equivalence between the cell release of lactate and H<sup>+</sup>. Finally, the simultaneous impairment of glucose-6P (G6P) degradation (by <i>H6PD</i> silencing) and hydrolysis (by silencing glucose-6-phosphatase) eventually results in a measurable ER collapse documenting the high-rate nature of G6P flux across the reticular membrane.

iScienceVol. 29(1)
Italian Institute of Technology (IT), Institute of Molecular Bioimaging and Physiology (IT), Ospedale Policlinico San Martino (IT), University of Genoa (IT)
Openalex Percentile: Top 57%
Endoplasmic Reticulum Stress and Disease
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