56 research outputs found

    Altered metabolic landscape in IDH‐mutant gliomas affects phospholipid, energy, and oxidative stress pathways

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    Heterozygous mutations in NADP‐dependent isocitrate dehydrogenases (IDH) define the large majority of diffuse gliomas and are associated with hypermethylation of DNA and chromatin. The metabolic dysregulations imposed by these mutations, whether dependent or not on the oncometabolite D‐2‐hydroxyglutarate (D2HG), are less well understood. Here, we applied mass spectrometry imaging on intracranial patient‐derived xenografts of IDH‐mutant versus IDH wild‐type glioma to profile the distribution of metabolites at high anatomical resolution in situ. This approach was complemented by in vivo tracing of labeled nutrients followed by liquid chromatography–mass spectrometry (LC‐MS) analysis. Selected metabolites were verified on clinical specimen. Our data identify remarkable differences in the phospholipid composition of gliomas harboring the IDH1 mutation. Moreover, we show that these tumors are characterized by reduced glucose turnover and a lower energy potential, correlating with their reduced aggressivity. Despite these differences, our data also show that D2HG overproduction does not result in a global aberration of the central carbon metabolism, indicating strong adaptive mechanisms at hand. Intriguingly, D2HG shows no quantitatively important glucose‐derived label in IDH‐mutant tumors, which suggests that the synthesis of this oncometabolite may rely on alternative carbon sources. Despite a reduction in NADPH, glutathione levels are maintained. We found that genes coding for key enzymes in de novo glutathione synthesis are highly expressed in IDH‐mutant gliomas and the expression of cystathionine‐β‐synthase (CBS) correlates with patient survival in the oligodendroglial subtype. This study provides a detailed and clinically relevant insight into the in vivo metabolism of IDH1‐mutant gliomas and points to novel metabolic vulnerabilities in these tumors

    Toxicity profile of bevacizumab in the UK Neurofibromatosis Type 2 cohort

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    Bevacizumab is considered an established part of the treatment strategies available for schwannomas in patients with Neurofibromatosis Type 2(NF2). In the UK, it is available through NHS National Specialized Commissioning to NF2 patients with a rapidly growing target schwannoma. Regrowth of the tumour on suspension of treatment is often observed resulting in prolonged periods of exposure to bevacizumab to control the disease. Hypertension and proteinuria are common events with bevacizumab use and there are concerns with regards to the long-term risks of prolonged treatment. Dosing, demographic and adverse event(CTCAE 4.03) data from the UK NF2 bevacizumab cohort are reviewed with particular consideration of renal and cardiovascular complications. Eighty patients (48 male:32female), median age 24.5 years (range 11-66years), were followed for a median of 32.7 months (range 12.0–60.2months). The most common adverse events were fatigue, hypertension and infection. A total of 19/80 patients (24%) had either a grade 2 or grade 3 hypertension event and 14/80 patients (17.5%) had proteinuria. Of 36 patients followed for 36 months, 78% were free from hypertension and 86% were free of proteinuria. Logistic regression modeling identified age and induction dosing regime to be predictors of development of hypertension with dose of 7.5mg/kg three weekly and age >30years having higher rates of hypertension. Proteinuria persisted in one of three patients after cessation of bevacizumab. One patient developed congestive heart failure and the details of this case are described. Further work is needed to determine optimal dosing regimes to limit toxicity without impacting on efficacy

    Modelling of the DIADEMO Experiment with the CATHARE Code for ASTRID Gas Power Conversion System Studies

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    International audienceThe Advanced Sodium Technological Reactor for Industrial Demonstration (ASTRID) is a French Sodiumcooled Fast Reactor developed by the CEA and its partners. For safety reasons, a gas Power Conversion System based on a nitrogen Brayton cycle is investigated for the tertiary circuit. One of the key issue is the design of an innovative Sodium Gas Heat Exchanger (SGHE) that transfers heat from the sodium secondary loops to the nitrogen Brayton cycle. The safety demonstration of this new option will require the thermohydraulic calculation of a wide range of normal and accidental situations that will be performed using the CATHARE-3 code. The first qualification step of the SGHE is to validate the thermo-hydraulic performances of the component and is carried out at low scale (40kW) on the DIADEMO loop currently in operation in Cadarache. This paper presents in details the modelling of the whole DIADEMO experiment with the CATHARE-3 code. The focus is made on the modelling of the SGHE but the modelling of the sodium and nitrogen loops and their components is also presented. The comparison between the experimental data and the CATHARE calculations is performed on a Loss Of Flow Accident (LOFA). For this LOFA, the blower's rotational speed is reduced and a bypass line is open in the nitrogen loop. Thisstudy extends the validation of the CATHARE code and justifies the modelling choices of the SGHE used for ASTRID transient studies
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