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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2014
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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. |
format | Online Article Text |
id | pubmed-4273974 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
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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