How Metabolomics Findings Can Drive New Therapeutic Approaches? (Volume II)

A special issue of Metabolites (ISSN 2218-1989). This special issue belongs to the section "Metabolomic Profiling Technology".

Deadline for manuscript submissions: closed (30 June 2022) | Viewed by 3168

Special Issue Editor


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Guest Editor
1. Biochemistry Department, Tours University Hospital, 37000 Tours, France
2. INSERM 1253, iBrain, University of Tours, Inserm, 37000 Tours, France
Interests: metabolomic analysis, amyotrophic lateral sclerosis; biomarkers
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Special Issue Information

Dear Colleagues,

Metabolism alteration is thoroughly involved in diverse pathologies from neurological diseases to cancer, either as a direct consequence of primary pathophysiological mechanisms or as an indirect process of disease evolution and/or patient management. For example, modifications of lipid metabolism, mitochondrial impairment, or glucose intolerance have largely been described in neurodegenerative diseases, as well as glycolysis modification in cancer. Omics studies have progressed in their technical aspects over recent years and have also led to putative clinical consequences. They have helped improve our knowledge of the metabolic pathways involved in these diseases and have provided hypotheses about their link with the main pathophysiological pathways like inflammation or oxidative stress. With regard to diseases with poor or ineffective therapeutics, many research groups are focused on the development of new strategies of treatment or new compounds based on metabolic targets. Importantly, metabolic perturbations linked to diseases or to new treatments or specific diets (i.e., ketogenic diet, vitamin supplementation, etc.) may play a prognostic role in these diseases.

In this context, it seems crucial to know how the increased practice of “omics” (mainly metabolomics and lipidomics) in in vitro, in vivo, and clinical studies may improve our capacity to identify new therapeutic targets and to follow the underlying, and perhaps hidden, effects of a given treatment. We should also pay attention to the subtle effects of changing diets, for example using this strategy in addition to other drugs or to use metabolism status to determine the subgroups of patients. Thus, omics approaches have many interests in healthcare, mainly as diagnosis and prognosis biomarkers—but we must keep in mind our ability to develop and monitor new therapeutic strategies based on their findings.

Accordingly, metabolomics and lipidomics studies that have enabled the characterization of subgroups of patients in clinical trials merit discussion in this Special Issue. Studies on metabolomics/lipidomics approaches that have identified therapeutic targets or studies evaluating, through in vitro or in vivo experiments, metabolic treatments directly targeting a metabolic pathway (glucose or lipid metabolism, respiratory chain, etc.) are relevant for highlighting the new opportunities in omics. Finally, reports of the deleterious, papers on the indirect consequences of metabolic disturbances associated with a treatment or a diet and that could play an important prognosis role are sought after for this Special Issue. 

Prof. Dr. Helene Blasco
Guest Editor

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Keywords

  • metabolomics
  • lipidomics
  • therapeutics
  • endophenotypes
  • disease monitoring

Published Papers (1 paper)

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Review

20 pages, 1341 KiB  
Review
Metabolomics as a Crucial Tool to Develop New Therapeutic Strategies for Neurodegenerative Diseases
by Débora Lanznaster, Giulia Dingeo, Rayhanatou Altine Samey, Patrick Emond and Hélène Blasco
Metabolites 2022, 12(9), 864; https://doi.org/10.3390/metabo12090864 - 14 Sep 2022
Cited by 2 | Viewed by 2924
Abstract
Neurodegenerative diseases (NDs), such as Alzheimer’s (AD), Parkinson’s (PD), and amyotrophic lateral sclerosis (ALS), share common pathological mechanisms, including metabolism alterations. However, their specific neuronal cell types affected and molecular biomarkers suggest that there are both common and specific alterations regarding metabolite levels. [...] Read more.
Neurodegenerative diseases (NDs), such as Alzheimer’s (AD), Parkinson’s (PD), and amyotrophic lateral sclerosis (ALS), share common pathological mechanisms, including metabolism alterations. However, their specific neuronal cell types affected and molecular biomarkers suggest that there are both common and specific alterations regarding metabolite levels. In this review, we were interested in identifying metabolite alterations that have been reported in preclinical models of NDs and that have also been documented as altered in NDs patients. Such alterations could represent interesting targets for the development of targeted therapy. Importantly, the translation of such findings from preclinical to clinical studies is primordial for the study of possible therapeutic agents. We found that N-acetyl-aspartate (NAA), myo-inositol, and glutamate are commonly altered in the three NDs investigated here. We also found other metabolites commonly altered in both AD and PD. In this review, we discuss the studies reporting such alterations and the possible pathological mechanism underlying them. Finally, we discuss clinical trials that have attempted to develop treatments targeting such alterations. We conclude that the treatment combination of both common and differential alterations would increase the chances of patients having access to efficient treatments for each ND. Full article
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