Neuroinflammation as a Factor of Neurodegenerative Disease: Thalidomide Analogs as Treatments

Neuroinflammation is initiated when glial cells, mainly microglia, are activated by threats to the neural environment, such as pathogen infiltration or neuronal injury. Although neuroinflammation serves to combat these threats and reinstate brain homeostasis, chronic inflammation can result in exces...

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Main Authors: Yoo Jin Jung, David Tweedie, Michael T. Scerba, Nigel H. Greig
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-12-01
Series:Frontiers in Cell and Developmental Biology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fcell.2019.00313/full
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spelling doaj-98f3f1c1c13a416cad5699044807bc502020-11-25T02:08:50ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2019-12-01710.3389/fcell.2019.00313497962Neuroinflammation as a Factor of Neurodegenerative Disease: Thalidomide Analogs as TreatmentsYoo Jin JungDavid TweedieMichael T. ScerbaNigel H. GreigNeuroinflammation is initiated when glial cells, mainly microglia, are activated by threats to the neural environment, such as pathogen infiltration or neuronal injury. Although neuroinflammation serves to combat these threats and reinstate brain homeostasis, chronic inflammation can result in excessive cytokine production and cell death if the cause of inflammation remains. Overexpression of tumor necrosis factor-α (TNF-α), a proinflammatory cytokine with a central role in microglial activation, has been associated with neuronal excitotoxicity, synapse loss, and propagation of the inflammatory state. Thalidomide and its derivatives, termed immunomodulatory imide drugs (IMiDs), are a class of drugs that target the 3′-untranslated region (3′-UTR) of TNF-α mRNA, inhibiting TNF-α production. Due to their multi-potent effects, several IMiDs, including thalidomide, lenalidomide, and pomalidomide, have been repurposed as drug treatments for diseases such as multiple myeloma and psoriatic arthritis. Preclinical studies of currently marketed IMiDs, as well as novel IMiDs such as 3,6′-dithiothalidomide and adamantyl thalidomide derivatives, support the development of IMiDs as therapeutics for neurological disease. IMiDs have a competitive edge compared to similar anti-inflammatory drugs due to their blood-brain barrier permeability and high bioavailability, with the potential to alleviate symptoms of neurodegenerative disease and slow disease progression. In this review, we evaluate the role of neuroinflammation in neurodegenerative diseases, focusing specifically on the role of TNF-α in neuroinflammation, as well as appraise current research on the potential of IMiDs as treatments for neurological disorders.https://www.frontiersin.org/article/10.3389/fcell.2019.00313/fullneuroinflammationtumor necrosis factor-α (TNF-α)neurodegenerationthalidomidelenalidomidepomalidomide
collection DOAJ
language English
format Article
sources DOAJ
author Yoo Jin Jung
David Tweedie
Michael T. Scerba
Nigel H. Greig
spellingShingle Yoo Jin Jung
David Tweedie
Michael T. Scerba
Nigel H. Greig
Neuroinflammation as a Factor of Neurodegenerative Disease: Thalidomide Analogs as Treatments
Frontiers in Cell and Developmental Biology
neuroinflammation
tumor necrosis factor-α (TNF-α)
neurodegeneration
thalidomide
lenalidomide
pomalidomide
author_facet Yoo Jin Jung
David Tweedie
Michael T. Scerba
Nigel H. Greig
author_sort Yoo Jin Jung
title Neuroinflammation as a Factor of Neurodegenerative Disease: Thalidomide Analogs as Treatments
title_short Neuroinflammation as a Factor of Neurodegenerative Disease: Thalidomide Analogs as Treatments
title_full Neuroinflammation as a Factor of Neurodegenerative Disease: Thalidomide Analogs as Treatments
title_fullStr Neuroinflammation as a Factor of Neurodegenerative Disease: Thalidomide Analogs as Treatments
title_full_unstemmed Neuroinflammation as a Factor of Neurodegenerative Disease: Thalidomide Analogs as Treatments
title_sort neuroinflammation as a factor of neurodegenerative disease: thalidomide analogs as treatments
publisher Frontiers Media S.A.
series Frontiers in Cell and Developmental Biology
issn 2296-634X
publishDate 2019-12-01
description Neuroinflammation is initiated when glial cells, mainly microglia, are activated by threats to the neural environment, such as pathogen infiltration or neuronal injury. Although neuroinflammation serves to combat these threats and reinstate brain homeostasis, chronic inflammation can result in excessive cytokine production and cell death if the cause of inflammation remains. Overexpression of tumor necrosis factor-α (TNF-α), a proinflammatory cytokine with a central role in microglial activation, has been associated with neuronal excitotoxicity, synapse loss, and propagation of the inflammatory state. Thalidomide and its derivatives, termed immunomodulatory imide drugs (IMiDs), are a class of drugs that target the 3′-untranslated region (3′-UTR) of TNF-α mRNA, inhibiting TNF-α production. Due to their multi-potent effects, several IMiDs, including thalidomide, lenalidomide, and pomalidomide, have been repurposed as drug treatments for diseases such as multiple myeloma and psoriatic arthritis. Preclinical studies of currently marketed IMiDs, as well as novel IMiDs such as 3,6′-dithiothalidomide and adamantyl thalidomide derivatives, support the development of IMiDs as therapeutics for neurological disease. IMiDs have a competitive edge compared to similar anti-inflammatory drugs due to their blood-brain barrier permeability and high bioavailability, with the potential to alleviate symptoms of neurodegenerative disease and slow disease progression. In this review, we evaluate the role of neuroinflammation in neurodegenerative diseases, focusing specifically on the role of TNF-α in neuroinflammation, as well as appraise current research on the potential of IMiDs as treatments for neurological disorders.
topic neuroinflammation
tumor necrosis factor-α (TNF-α)
neurodegeneration
thalidomide
lenalidomide
pomalidomide
url https://www.frontiersin.org/article/10.3389/fcell.2019.00313/full
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