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Chemical Genetics Screening Reveals KIAA1363 as a Cytokine-Lowering Target

[Image: see text] Inflammation is a hallmark of many human diseases, including pain, arthritis, atherosclerosis, obesity and diabetes, cancer, and neurodegenerative diseases. Although there are several successfully marketed small molecules anti-inflammatory drugs such as cyclooxygenase inhibitors an...

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Autores principales: Hunerdosse, Devon M., Morris, Patrick J., Miyamoto, David K., Fisher, Karl J., Bateman, Leslie A., Ghazaleh, Jonathan R., Zhong, Sharon, Nomura, Daniel K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4273974/
https://www.ncbi.nlm.nih.gov/pubmed/25343321
http://dx.doi.org/10.1021/cb500717g
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author Hunerdosse, Devon M.
Morris, Patrick J.
Miyamoto, David K.
Fisher, Karl J.
Bateman, Leslie A.
Ghazaleh, Jonathan R.
Zhong, Sharon
Nomura, Daniel K.
author_facet Hunerdosse, Devon M.
Morris, Patrick J.
Miyamoto, David K.
Fisher, Karl J.
Bateman, Leslie A.
Ghazaleh, Jonathan R.
Zhong, Sharon
Nomura, Daniel K.
author_sort Hunerdosse, Devon M.
collection PubMed
description [Image: see text] Inflammation is a hallmark of many human diseases, including pain, arthritis, atherosclerosis, obesity and diabetes, cancer, and neurodegenerative diseases. Although there are several successfully marketed small molecules anti-inflammatory drugs such as cyclooxygenase inhibitors and glucocorticoids, many of these compounds are also associated with various adverse cardiovascular or immunosuppressive side effects. Thus, identifying novel anti-inflammatory small molecules and their targets is critical for developing safer and more effective next-generation treatment strategies for inflammatory diseases. Here, we have conducted a chemical genetics screen to identify small molecules that suppress the release of the inflammatory cytokine TNFα from stimulated macrophages. We have used an enzyme class-directed chemical library for our screening efforts to facilitate subsequent target identification using activity-based protein profiling (ABPP). Using this strategy, we have found that KIAA1363 is a novel target for lowering key pro-inflammatory cytokines through affecting key ether lipid metabolism pathways. Our study highlights the application of combining chemical genetics with chemoproteomic and metabolomic approaches toward identifying and characterizing anti-inflammatory smal molecules and their targets.
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spelling pubmed-42739742015-10-24 Chemical Genetics Screening Reveals KIAA1363 as a Cytokine-Lowering Target Hunerdosse, Devon M. Morris, Patrick J. Miyamoto, David K. Fisher, Karl J. Bateman, Leslie A. Ghazaleh, Jonathan R. Zhong, Sharon Nomura, Daniel K. ACS Chem Biol [Image: see text] Inflammation is a hallmark of many human diseases, including pain, arthritis, atherosclerosis, obesity and diabetes, cancer, and neurodegenerative diseases. Although there are several successfully marketed small molecules anti-inflammatory drugs such as cyclooxygenase inhibitors and glucocorticoids, many of these compounds are also associated with various adverse cardiovascular or immunosuppressive side effects. Thus, identifying novel anti-inflammatory small molecules and their targets is critical for developing safer and more effective next-generation treatment strategies for inflammatory diseases. Here, we have conducted a chemical genetics screen to identify small molecules that suppress the release of the inflammatory cytokine TNFα from stimulated macrophages. We have used an enzyme class-directed chemical library for our screening efforts to facilitate subsequent target identification using activity-based protein profiling (ABPP). Using this strategy, we have found that KIAA1363 is a novel target for lowering key pro-inflammatory cytokines through affecting key ether lipid metabolism pathways. Our study highlights the application of combining chemical genetics with chemoproteomic and metabolomic approaches toward identifying and characterizing anti-inflammatory smal molecules and their targets. American Chemical Society 2014-10-24 2014-12-19 /pmc/articles/PMC4273974/ /pubmed/25343321 http://dx.doi.org/10.1021/cb500717g Text en Copyright © 2014 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Hunerdosse, Devon M.
Morris, Patrick J.
Miyamoto, David K.
Fisher, Karl J.
Bateman, Leslie A.
Ghazaleh, Jonathan R.
Zhong, Sharon
Nomura, Daniel K.
Chemical Genetics Screening Reveals KIAA1363 as a Cytokine-Lowering Target
title Chemical Genetics Screening Reveals KIAA1363 as a Cytokine-Lowering Target
title_full Chemical Genetics Screening Reveals KIAA1363 as a Cytokine-Lowering Target
title_fullStr Chemical Genetics Screening Reveals KIAA1363 as a Cytokine-Lowering Target
title_full_unstemmed Chemical Genetics Screening Reveals KIAA1363 as a Cytokine-Lowering Target
title_short Chemical Genetics Screening Reveals KIAA1363 as a Cytokine-Lowering Target
title_sort chemical genetics screening reveals kiaa1363 as a cytokine-lowering target
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4273974/
https://www.ncbi.nlm.nih.gov/pubmed/25343321
http://dx.doi.org/10.1021/cb500717g
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