Author

E. H. Gilglioni

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Biochemistry· 2 Cancer Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:metabolism & bioenergetics· 3 Organism:human· 2 Assay:metabolomics· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell signaling & trafficking· 1 Organism:mouse· 1 Assay:proteomics· 1

Frequent Co-Authors

A. J. Verhoeven· 2 shared H. L. Li· 2 shared J.-C. Chang· 2 shared S. Go· 2 shared A. Li· 1 shared A. Prasnicka· 1 shared D. C. Hay· 1 shared D. Ezerina· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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2 shared papersBiochemistry

A. J. Verhoeven

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Author profile →

3 papers

Recent·Most cited

Protein tyrosine phosphatase receptor kappa regulates glycolysis and de novo lipogenesis to promote hepatocyte metabolic reprogramming in obesity

E. H. Gilglioni, A. Li, W. Saint-Pierre Wijckmans, T.-K. Shen, I. Perez-Chavez, G. Hovhannisyan, M. Lisjak, J. Negueruela, V. Vandenbempt, J. Bauza-Martinez, J. M. Herranz, D. Ezerina, S. Demine, Z. Feng, T. Vignane, , E. N. Gurzov

This study identifies PTPRK's role in promoting hepatocyte metabolic reprogramming in obesity by regulating glycolysis and lipogenesis, with potential therapeutic implications for obesity-related liver diseases.

bioRxiv · Dec 1, 2023 · PreprintCancer Biology

Opposite regulation of glycogen metabolism by cAMP produced in the cytosol and at the plasma membrane

A. J. Verhoeven, P. F. V. Bizerra, E. H. Gilglioni, S. Go, H. L. Li, R. P. J. O. Elferink, J.-C. Chang

This study shows that cAMP produced at the plasma membrane promotes glycogen breakdown, while cAMP produced in the cytosol inhibits it, highlighting the role of cAMP microdomain organization in glycogen metabolism.

bioRxiv · Sep 1, 2022 · PreprintBiochemistry

Non-canonical regulation of glycogenolysis and the Warburg phenotype by soluble adenylyl cyclase

J.-C. Chang, S. Go, E. H. Gilglioni, H. L. Li, H.-L. Huang, L. R. Levin, J. Buck, A. J. Verhoeven, R. P. J. Oude Elferink

This study shows that soluble adenylyl cyclase (sAC) regulates glycogenolysis and the Warburg phenotype by modulating cAMP signaling pathways.

bioRxiv · Feb 2, 2020 · PreprintBiochemistry