Laurent Fernando

ORCID: 0000-0002-2816-4037
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About
Contact & Profiles
Research Areas
  • Acute Myeloid Leukemia Research
  • Histone Deacetylase Inhibitors Research
  • Epigenetics and DNA Methylation
  • Microbial Natural Products and Biosynthesis
  • Chemical Synthesis and Analysis
  • Computational Drug Discovery Methods

École Nationale Vétérinaire de Toulouse
2019-2021

Université de Toulouse
2019-2021

Université Toulouse III - Paul Sabatier
2019-2021

Toxalim Research Centre in Food Toxicology
2017-2019

European Bioinformatics Institute
2018

Mutations in IDH induce epigenetic and transcriptional reprogramming, differentiation bias, susceptibility to mitochondrial inhibitors cancer cells. Here, we first show that cell lines, PDXs, patients with acute myeloid leukemia (AML) harboring an mutation displayed enhanced oxidative metabolism. Along increase TCA cycle intermediates, this AML-specific metabolic behavior mechanistically occurred through the electron transport chain complex I activity, respiration, methylation-driven...

10.1084/jem.20200924 article EN cc-by-nc-sa The Journal of Experimental Medicine 2021-03-24

There are numerous applications that use the structures of protein-ligand complexes from PDB, such as 3D pharmacophore identification, virtual screening, and fragment-based drug design. The underlying these potentially much more informative if they contain biologically relevant bound ligands, with high similarity to cognate ligands. We present a study ligand-enzyme compares enabling best matches be identified. calculate molecular scores using method called PARITY (proportion atoms residing...

10.1016/j.str.2018.02.009 article EN cc-by Structure 2018-03-15

Isocitrate dehydrogenases (IDH) are involved in redox control and central metabolism. We hypothesized that key metabolic fluxes selectively reprogrammed to maintain biosynthetic homeostasis lower drug responses IDH mutant acute myeloid leukemia cells. Here we show reprogramming initiated by IDH1 mutation leads marked increases glucose, glutamine fatty acid catabolism along with enhancement of wild-type enzyme activity contribute provision α-KG required for 2-HG synthesis replenish Krebs...

10.2139/ssrn.3255557 article EN SSRN Electronic Journal 2018-01-01

Isocitrate dehydrogenases (IDH) are involved in redox control and central metabolism. Mutations IDH induce epigenetic transcriptional reprogramming, differentiation bias, BCL-2 dependence susceptibility to mitochondrial inhibitors cancer cells. Here we show that high sensitivity oxidative phosphorylation (OxPHOS) is due an enhanced metabolism cell lines, PDX patients with acute myeloid leukemia (AML) harboring mutation. Along increase TCA cycle intermediates, this AML-specific metabolic...

10.1101/749580 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2019-08-28
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