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1.
J Neurooncol ; 139(2): 369-372, 2018 Sep.
Article in English | MEDLINE | ID: mdl-29700673

ABSTRACT

INTRODUCTION: There is currently no treatment for solitary fibrous tumors/hemangiopericytomas (SFT/H) of the central nervous system recurring after multiple surgeries and radiotherapies. The NAB2-STAT6 gene fusion is the hallmark of these tumors, and upregulates Early Growth Factor, activating several growth pathways. METHODS: We treated two patients presenting pluri-recurrent meningeal SFT/H with Pazopanib, a broad-spectrum tyrosine kinase inhibitor. We analyzed the exome and RNA sequencing data of one of them and, in addition to another meningeal SFT/H, compared it to the transcriptomic profiling of 5 systemic SFT/H. RESULTS: A dramatic clinical and radiological response was observed in both cases, respectively 84 and 43% decrease after 3 months. As a comparison, Pazopanib has only a stabilizing effect in systemic SFT/H. Indeed, central nervous system SFT/H show overexpression of different tyrosine kinases targeted by Pazopanib. CONCLUSIONS: Two consecutive patients with untreatable central nervous system SFT/H showed a spectacular partial response to Pazopanib, an unprecedented result in SFT/H. This result could be explained by differences in expression profiles and calls for a confirmation in a larger cohort of patients.


Subject(s)
Angiogenesis Inhibitors/therapeutic use , Central Nervous System Neoplasms/drug therapy , Hemangiopericytoma/drug therapy , Neoplasm Recurrence, Local/drug therapy , Pyrimidines/therapeutic use , Solitary Fibrous Tumors/drug therapy , Sulfonamides/therapeutic use , Adult , Central Nervous System Neoplasms/diagnostic imaging , Central Nervous System Neoplasms/metabolism , Female , Hemangiopericytoma/diagnostic imaging , Hemangiopericytoma/metabolism , Humans , Indazoles , Male , Middle Aged , Neoplasm Recurrence, Local/diagnostic imaging , Neoplasm Recurrence, Local/metabolism , Solitary Fibrous Tumors/diagnostic imaging , Solitary Fibrous Tumors/metabolism , Treatment Outcome
2.
Plant J ; 81(6): 947-60, 2015 Mar.
Article in English | MEDLINE | ID: mdl-25645872

ABSTRACT

Upon nutrient deprivation, microalgae partition photosynthate into starch and lipids at the expense of protein synthesis and growth. We investigated the role of starch biosynthesis with respect to photosynthetic growth and carbon partitioning in the Chlamydomonas reinhardtii starchless mutant, sta6, which lacks ADP-glucose pyrophosphorylase. This mutant is unable to convert glucose-1-phosphate to ADP-glucose, the precursor of starch biosynthesis. During nutrient-replete culturing, sta6 does not re-direct metabolism to make more proteins or lipids, and accumulates 20% less biomass. The underlying molecular basis for the decreased biomass phenotype was identified using LC-MS metabolomics studies and flux methods. Above a threshold light intensity, photosynthetic electron transport rates (water → CO2) decrease in sta6 due to attenuated rates of NADPH re-oxidation, without affecting photosystems I or II (no change in isolated photosynthetic electron transport). We observed large accumulations of carbon metabolites that are precursors for the biosynthesis of lipids, amino acids and sugars/starch, indicating system-wide consequences of slower NADPH re-oxidation. Attenuated carbon fixation resulted in imbalances in both redox and adenylate energy. The pool sizes of both pyridine and adenylate nucleotides in sta6 increased substantially to compensate for the slower rate of turnover. Mitochondrial respiration partially relieved the reductant stress; however, prolonged high-light exposure caused accelerated photoinhibition. Thus, starch biosynthesis in Chlamydomonas plays a critical role as a principal carbon sink influencing cellular energy balance however, disrupting starch biosynthesis does not redirect resources to other bioproducts (lipids or proteins) during nutrient-replete culturing, resulting in cells that are susceptible to photochemical damage caused by redox stress.


Subject(s)
Chlamydomonas reinhardtii/metabolism , Glucose-1-Phosphate Adenylyltransferase/genetics , Starch/metabolism , Algal Proteins/genetics , Algal Proteins/metabolism , Biomass , Carbon/metabolism , Chlamydomonas reinhardtii/genetics , Electron Transport , Glucose-1-Phosphate Adenylyltransferase/metabolism , Glucosephosphates/metabolism , Light , Metabolomics , Mutation , NADP/metabolism , Oxidation-Reduction , Phenotype , Photosynthesis , Photosystem I Protein Complex/metabolism , Photosystem II Protein Complex/metabolism
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