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Extracellular glutamate and IDH1R132H inhibitor promote glioma growth by boosting redox potential

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Journal of Neuro-Oncology Aims and scope Submit manuscript

Abstract

Purpose

Somatic mutations of the isocitrate dehydrogenase 1 (IDH1) gene, mostly substituting Arg132 with histidine, are associated with better patient survival, but glioma recurrence and progression are nearly inevitable, resulting in disproportionate morbidity and mortality. Our previous studies demonstrated that in contrast to hemizygous IDH1R132H (loss of wild-type allele), heterozygous IDH1R132H is intrinsically glioma suppressive but its suppression of three-dimensional (3D) growth is negated by extracellular glutamate and reducing equivalent. This study sought to understand the importance of 3D culture in IDH1R132H biology and the underlying mechanism of the glutamate effect.

Methods

RNA sequencing data of IDH1R132H-heterozygous and IDH1R132H-hemizygous glioma cells cultured under two-dimensional (2D) and 3D conditions were subjected to unsupervised hierarchal clustering and gene set enrichment analysis. IDH1R132H-heterozygous and IDH1R132H-hemizygous tumor growth were compared in subcutaneous and intracranial transplantations. Short-hairpin RNA against glutamate dehydrogenase 2 gene (GLUD2) expression was employed to determine the effects of glutamate and the mutant IDH1 inhibitor AGI-5198 on redox potential in IDH1R132H-heterozygous cells.

Results

In contrast to IDH1R132H-heterozygous cells, 3D-cultured but not 2D-cultured IDH1R132H-hemizygous cells were clustered with more malignant gliomas, possessed the glioblastoma mesenchymal signature, and exhibited aggressive tumor growth. Although both extracellular glutamate and AGI-5198 stimulated redox potential for 3D growth of IDH1R132H-heterozygous cells, GLUD2 expression was required for glutamate, but not AGI-5198, stimulation.

Conclusion

3D culture is more relevant to IDH1R132H glioma biology. The importance of redox homeostasis in IDH1R132H glioma suggests that metabolic pathway(s) can be explored for therapeutic targeting, whereas IDH1R132H inhibitors may have counterproductive consequences in patient treatment.

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Acknowledgements

Research reported in this publication utilized the High-Throughput Genomics and Bioinformatic Analysis Shared Resource and the Biorepository and Molecular Pathology Shared Resource at Huntsman Cancer Institute at the University of Utah. This work was supported in part by funds in conjunction with grant P30 CA042014 from the National Cancer Institute of the National Institutes of Health. This work was supported in part by the National Institute of Neurological Disorders and Stroke R21NS108065 Grant. The authors thank Chris Stubben for providing consultation for the analysis of RNA sequencing data, Luming Zhou and Carl T. Wittwer for the assistance in quantitative PCR analysis, Laura Roberts for technical assistance, and Kristin Kraus for editorial assistance.

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Authors and Affiliations

  1. Department of Neurosurgery, Clinical Neurosciences Center, University of Utah, Salt Lake City, UT 84132, USA

    Patricia D. B. Tiburcio, David L. Gillespie, Randy L. Jensen & L. Eric Huang

  2. Department of Oncological Sciences, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT 84112, USA

    Patricia D. B. Tiburcio, Randy L. Jensen & L. Eric Huang

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  1. Patricia D. B. Tiburcio
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Correspondence to L. Eric Huang.

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Tiburcio, P.D.B., Gillespie, D.L., Jensen, R.L. et al. Extracellular glutamate and IDH1R132H inhibitor promote glioma growth by boosting redox potential. J Neurooncol 146, 427–437 (2020). https://doi.org/10.1007/s11060-019-03359-w

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