Arylamine N-acetyltransferase 1 expression predicts glucose dependence and mitochondrial bioenergetics in cancer cells

To investigate the effects of varying NAT1 activity in different cell lines, mitochondrial oxidative phosphorylation, aerobic glycolysis and mitochondrial fuel usage was quantified in a panel of human cell lines. As NAT1 activity increased, mitochondrial reserve respiratory capacity increased while aerobic glycolysis decreased. In addition, phosphorylation of PDH-E1α in these cells limited their ability to use glucose as a primary fuel source. Those cells with high NAT1 activity exhibited a quiescent metabolic phenotype and proliferated more slowly. This might explain, in part, why some cancer patients with low NAT1 expression in their tumour tissue show poorer survival outcomes compared to those with high NAT1 expression. The current study demonstrated that NAT1 enzymatic activity is important for metabolism in cancer cell lines and increasing NAT1 activity may better equip cells to survive under stressed conditions by increasing reserve respiratory capacity.

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Publication Details

Journal
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research
Published
2025-03-05
DOI
https://doi.org/10.1016/j.bbamcr.2025.119929
Citations
1
Primary Topic
Diet and metabolism studies
Type
article
Field-Weighted Citation Impact
1.16
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article

Arylamine N-acetyltransferase 1 expression predicts glucose dependence and mitochondrial bioenergetics in cancer cells

Rodney F. Minchin, Neville J. Butcher, Chandra Choudhury
1 citations
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research
Diet and metabolism studies
1.16
article

Arylamine N-acetyltransferase 1 expression predicts glucose dependence and mitochondrial bioenergetics in cancer cells

Rodney F. Minchin, Neville J. Butcher, Chandra Choudhury
article en
1 citations

Abstract

To investigate the effects of varying NAT1 activity in different cell lines, mitochondrial oxidative phosphorylation, aerobic glycolysis and mitochondrial fuel usage was quantified in a panel of human cell lines. As NAT1 activity increased, mitochondrial reserve respiratory capacity increased while aerobic glycolysis decreased. In addition, phosphorylation of PDH-E1α in these cells limited their ability to use glucose as a primary fuel source. Those cells with high NAT1 activity exhibited a quiescent metabolic phenotype and proliferated more slowly. This might explain, in part, why some cancer patients with low NAT1 expression in their tumour tissue show poorer survival outcomes compared to those with high NAT1 expression. The current study demonstrated that NAT1 enzymatic activity is important for metabolism in cancer cell lines and increasing NAT1 activity may better equip cells to survive under stressed conditions by increasing reserve respiratory capacity.

Biochimica et Biophysica Acta (BBA) - Molecular Cell ResearchVol. 1872(4)
The University of Queensland (AU)
Zero hunger
Openalex Percentile: Top 25%
Diet and metabolism studies
1.16
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