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HMGA2-mediated glutamine metabolism is required for Cd-induced cell growth and cell migration.
- Source :
-
Toxicology [Toxicology] 2024 Sep; Vol. 507, pp. 153899. Date of Electronic Publication: 2024 Jul 19. - Publication Year :
- 2024
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Abstract
- Cadmium (Cd) exposure significantly increases the risk of lung cancer. The demand for glutamine is increasing in cancers, including lung cancer. In this study, we investigated the role of glutamine metabolism in Cd-induced cell growth and migration. Firstly, we found that 2 μM Cd-treatment up-regulated the expression of ASCT2 (alanine, serine, cysteine-preferring transporter 2) and ASNS (asparagine synthetase) while downregulating mitochondrial glutaminase GLS1 in A549 cells. The same results were obtained in male BALB/c mice treated with 0.5 and 1 mg Cd/kg body weight. Subsequently, both glutamine deprivation and transfection with siASCT2 revealed that glutamine played a role in Cd-induced cell growth and migration. Furthermore, using 4-PBA (5 mM), an inhibitor of endoplasmic reticulum (ER) stress, Tm (0.1 μg/ml), an inducer of ER stress, siHMGA2, and over-expressing HMGA2 plasmids we demonstrated that ER stress/HMGA2 axis was involved in inducing ASCT2 and ASNS, while inhibiting GLS1. Additionally, the chromatin immunoprecipitation assay using an HMGA2 antibody revealed the direct binding of the HMGA2 to the promoter sequences of the ASCT2, ASNS, and GLS1 genes. Finally, dual luciferase reporter assay determined that HMGA2 increased the transcription of ASCT2 and ASNS while inhibiting the transcription of GLS1. Overall, we found that ER stress-induced HMGA2 controls glutamine metabolism by transcriptional regulation of ASCT2, ASNS and GLS1 to accelerate cell growth and migration during exposure to Cd at low concentrations. This study innovatively revealed the mechanism of Cd-induced cell growth which offers a fresh perspective on preventing Cd toxicity through glutamine metabolism.<br />Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 Elsevier B.V. All rights reserved.)
- Subjects :
- Animals
Humans
Male
Mice
A549 Cells
Cadmium toxicity
Cell Proliferation drug effects
Endoplasmic Reticulum Stress drug effects
Glutaminase metabolism
Glutaminase genetics
Mice, Inbred BALB C
Amino Acid Transport System ASC metabolism
Amino Acid Transport System ASC genetics
Cell Movement drug effects
Glutamine metabolism
HMGA2 Protein metabolism
HMGA2 Protein genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1879-3185
- Volume :
- 507
- Database :
- MEDLINE
- Journal :
- Toxicology
- Publication Type :
- Academic Journal
- Accession number :
- 39032683
- Full Text :
- https://doi.org/10.1016/j.tox.2024.153899