The therapeutic effects of 4-phenylbutyric acid in maintaining proteostasis
Recently, there has been an increasing amount of literature published on the effects of 4-phenylbutyric acid (4-PBA) in various biological systems. 4-PBA is currently used clinically to treat urea cycle disorders under the trade name Buphenyl. Recent studies however have explored 4-PBA in the contex...
Gespeichert in:
Veröffentlicht in: | The international journal of biochemistry & cell biology 2015-04, Vol.61, p.45-52 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 52 |
---|---|
container_issue | |
container_start_page | 45 |
container_title | The international journal of biochemistry & cell biology |
container_volume | 61 |
creator | Kolb, P.S. Ayaub, E.A. Zhou, W. Yum, V. Dickhout, J.G. Ask, K. |
description | Recently, there has been an increasing amount of literature published on the effects of 4-phenylbutyric acid (4-PBA) in various biological systems. 4-PBA is currently used clinically to treat urea cycle disorders under the trade name Buphenyl. Recent studies however have explored 4-PBA in the context of a low weight molecular weight chemical chaperone. Its properties as a chemical chaperone prevent misfolded protein aggregation and alleviate endoplasmic reticulum (ER) stress. As the ER is responsible for folding proteins targeted for use in membranes or secreted out of the cell, failure of maintaining adequate ER homeostasis may lead to protein misfolding and subsequent cell and organ pathology. Accumulation of misfolded proteins within the ER activates the unfolded protein response (UPR), a molecular repair response. The activation of the UPR aims to restore ER and cellular proteostasis by regulating the rate of synthesis of newly formed proteins as well as initiating molecular programs aimed to help fold or degrade misfolded proteins. If proteostasis is not restored, the UPR may initiate pro-apoptotic pathways. It is suggested that 4-PBA may help fold proteins in the ER, attenuating the activation of the UPR, and thus potentially alleviating various pathologies. This review discusses the biomedical research exploring the potential therapeutic effects of 4-PBA in various in vitro and in vivo model systems and clinical trials, while also commenting on the possible mechanisms of action. |
doi_str_mv | 10.1016/j.biocel.2015.01.015 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1677885172</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1357272515000254</els_id><sourcerecordid>1677885172</sourcerecordid><originalsourceid>FETCH-LOGICAL-c428t-2c74a965d918623ad9437ed310e1ad76f5cf2e69655ba817e77320b64dcf74f13</originalsourceid><addsrcrecordid>eNp9kF1LwzAUhoMobk7_gUgvvWlN0iZpbwQZfuHAm3kd0uTEZWztTFJh_96MTi-FExI4z8nLeRC6JrggmPC7ddG6XsOmoJiwApNU7ARNSS3qnNWCnaZ3yUROBWUTdBHCGuOE0PIcTSjjHJe8maK35QqyuAKvdjBEpzOwFnQMWW-zKt-toNtv2iHufWop7UzmumyrXBfTcd1ntvN9hD5EFVy4RGdWbQJcHe8Z-nh6XM5f8sX78-v8YZHritYxp1pUquHMNKTmtFSmqUoBpiQYiDKCW6YtBZ4I1qqaCBCipLjlldFWVJaUM3Q7_pvCvwYIUW5dSCY2qoN-CJJwIeqaEUETWo2o9n0IHqzcebdVfi8JlgeNci1HjfKgUWKSiqWxm2PC0G7B_A39ekvA_QhA2vPbgZdBO-g0GOeTPml693_CD0cThU8</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1677885172</pqid></control><display><type>article</type><title>The therapeutic effects of 4-phenylbutyric acid in maintaining proteostasis</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Kolb, P.S. ; Ayaub, E.A. ; Zhou, W. ; Yum, V. ; Dickhout, J.G. ; Ask, K.</creator><creatorcontrib>Kolb, P.S. ; Ayaub, E.A. ; Zhou, W. ; Yum, V. ; Dickhout, J.G. ; Ask, K.</creatorcontrib><description>Recently, there has been an increasing amount of literature published on the effects of 4-phenylbutyric acid (4-PBA) in various biological systems. 4-PBA is currently used clinically to treat urea cycle disorders under the trade name Buphenyl. Recent studies however have explored 4-PBA in the context of a low weight molecular weight chemical chaperone. Its properties as a chemical chaperone prevent misfolded protein aggregation and alleviate endoplasmic reticulum (ER) stress. As the ER is responsible for folding proteins targeted for use in membranes or secreted out of the cell, failure of maintaining adequate ER homeostasis may lead to protein misfolding and subsequent cell and organ pathology. Accumulation of misfolded proteins within the ER activates the unfolded protein response (UPR), a molecular repair response. The activation of the UPR aims to restore ER and cellular proteostasis by regulating the rate of synthesis of newly formed proteins as well as initiating molecular programs aimed to help fold or degrade misfolded proteins. If proteostasis is not restored, the UPR may initiate pro-apoptotic pathways. It is suggested that 4-PBA may help fold proteins in the ER, attenuating the activation of the UPR, and thus potentially alleviating various pathologies. This review discusses the biomedical research exploring the potential therapeutic effects of 4-PBA in various in vitro and in vivo model systems and clinical trials, while also commenting on the possible mechanisms of action.</description><identifier>ISSN: 1357-2725</identifier><identifier>EISSN: 1878-5875</identifier><identifier>DOI: 10.1016/j.biocel.2015.01.015</identifier><identifier>PMID: 25660369</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>4-PBA ; 4-Phenylbutyric acid ; Animals ; Endoplasmic Reticulum - drug effects ; Endoplasmic Reticulum - metabolism ; Endoplasmic Reticulum Stress - drug effects ; ER stress ; Homeostasis ; Humans ; Phenylbutyrates - pharmacology ; Phenylbutyrates - therapeutic use ; Signal Transduction ; Unfolded Protein Response - drug effects ; UPR ; Urea Cycle Disorders, Inborn - drug therapy</subject><ispartof>The international journal of biochemistry & cell biology, 2015-04, Vol.61, p.45-52</ispartof><rights>2015 Elsevier Ltd</rights><rights>Copyright © 2015 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c428t-2c74a965d918623ad9437ed310e1ad76f5cf2e69655ba817e77320b64dcf74f13</citedby><cites>FETCH-LOGICAL-c428t-2c74a965d918623ad9437ed310e1ad76f5cf2e69655ba817e77320b64dcf74f13</cites><orcidid>0000-0002-0202-735X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1357272515000254$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25660369$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kolb, P.S.</creatorcontrib><creatorcontrib>Ayaub, E.A.</creatorcontrib><creatorcontrib>Zhou, W.</creatorcontrib><creatorcontrib>Yum, V.</creatorcontrib><creatorcontrib>Dickhout, J.G.</creatorcontrib><creatorcontrib>Ask, K.</creatorcontrib><title>The therapeutic effects of 4-phenylbutyric acid in maintaining proteostasis</title><title>The international journal of biochemistry & cell biology</title><addtitle>Int J Biochem Cell Biol</addtitle><description>Recently, there has been an increasing amount of literature published on the effects of 4-phenylbutyric acid (4-PBA) in various biological systems. 4-PBA is currently used clinically to treat urea cycle disorders under the trade name Buphenyl. Recent studies however have explored 4-PBA in the context of a low weight molecular weight chemical chaperone. Its properties as a chemical chaperone prevent misfolded protein aggregation and alleviate endoplasmic reticulum (ER) stress. As the ER is responsible for folding proteins targeted for use in membranes or secreted out of the cell, failure of maintaining adequate ER homeostasis may lead to protein misfolding and subsequent cell and organ pathology. Accumulation of misfolded proteins within the ER activates the unfolded protein response (UPR), a molecular repair response. The activation of the UPR aims to restore ER and cellular proteostasis by regulating the rate of synthesis of newly formed proteins as well as initiating molecular programs aimed to help fold or degrade misfolded proteins. If proteostasis is not restored, the UPR may initiate pro-apoptotic pathways. It is suggested that 4-PBA may help fold proteins in the ER, attenuating the activation of the UPR, and thus potentially alleviating various pathologies. This review discusses the biomedical research exploring the potential therapeutic effects of 4-PBA in various in vitro and in vivo model systems and clinical trials, while also commenting on the possible mechanisms of action.</description><subject>4-PBA</subject><subject>4-Phenylbutyric acid</subject><subject>Animals</subject><subject>Endoplasmic Reticulum - drug effects</subject><subject>Endoplasmic Reticulum - metabolism</subject><subject>Endoplasmic Reticulum Stress - drug effects</subject><subject>ER stress</subject><subject>Homeostasis</subject><subject>Humans</subject><subject>Phenylbutyrates - pharmacology</subject><subject>Phenylbutyrates - therapeutic use</subject><subject>Signal Transduction</subject><subject>Unfolded Protein Response - drug effects</subject><subject>UPR</subject><subject>Urea Cycle Disorders, Inborn - drug therapy</subject><issn>1357-2725</issn><issn>1878-5875</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kF1LwzAUhoMobk7_gUgvvWlN0iZpbwQZfuHAm3kd0uTEZWztTFJh_96MTi-FExI4z8nLeRC6JrggmPC7ddG6XsOmoJiwApNU7ARNSS3qnNWCnaZ3yUROBWUTdBHCGuOE0PIcTSjjHJe8maK35QqyuAKvdjBEpzOwFnQMWW-zKt-toNtv2iHufWop7UzmumyrXBfTcd1ntvN9hD5EFVy4RGdWbQJcHe8Z-nh6XM5f8sX78-v8YZHritYxp1pUquHMNKTmtFSmqUoBpiQYiDKCW6YtBZ4I1qqaCBCipLjlldFWVJaUM3Q7_pvCvwYIUW5dSCY2qoN-CJJwIeqaEUETWo2o9n0IHqzcebdVfi8JlgeNci1HjfKgUWKSiqWxm2PC0G7B_A39ekvA_QhA2vPbgZdBO-g0GOeTPml693_CD0cThU8</recordid><startdate>20150401</startdate><enddate>20150401</enddate><creator>Kolb, P.S.</creator><creator>Ayaub, E.A.</creator><creator>Zhou, W.</creator><creator>Yum, V.</creator><creator>Dickhout, J.G.</creator><creator>Ask, K.</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0202-735X</orcidid></search><sort><creationdate>20150401</creationdate><title>The therapeutic effects of 4-phenylbutyric acid in maintaining proteostasis</title><author>Kolb, P.S. ; Ayaub, E.A. ; Zhou, W. ; Yum, V. ; Dickhout, J.G. ; Ask, K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c428t-2c74a965d918623ad9437ed310e1ad76f5cf2e69655ba817e77320b64dcf74f13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>4-PBA</topic><topic>4-Phenylbutyric acid</topic><topic>Animals</topic><topic>Endoplasmic Reticulum - drug effects</topic><topic>Endoplasmic Reticulum - metabolism</topic><topic>Endoplasmic Reticulum Stress - drug effects</topic><topic>ER stress</topic><topic>Homeostasis</topic><topic>Humans</topic><topic>Phenylbutyrates - pharmacology</topic><topic>Phenylbutyrates - therapeutic use</topic><topic>Signal Transduction</topic><topic>Unfolded Protein Response - drug effects</topic><topic>UPR</topic><topic>Urea Cycle Disorders, Inborn - drug therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kolb, P.S.</creatorcontrib><creatorcontrib>Ayaub, E.A.</creatorcontrib><creatorcontrib>Zhou, W.</creatorcontrib><creatorcontrib>Yum, V.</creatorcontrib><creatorcontrib>Dickhout, J.G.</creatorcontrib><creatorcontrib>Ask, K.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The international journal of biochemistry & cell biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kolb, P.S.</au><au>Ayaub, E.A.</au><au>Zhou, W.</au><au>Yum, V.</au><au>Dickhout, J.G.</au><au>Ask, K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The therapeutic effects of 4-phenylbutyric acid in maintaining proteostasis</atitle><jtitle>The international journal of biochemistry & cell biology</jtitle><addtitle>Int J Biochem Cell Biol</addtitle><date>2015-04-01</date><risdate>2015</risdate><volume>61</volume><spage>45</spage><epage>52</epage><pages>45-52</pages><issn>1357-2725</issn><eissn>1878-5875</eissn><abstract>Recently, there has been an increasing amount of literature published on the effects of 4-phenylbutyric acid (4-PBA) in various biological systems. 4-PBA is currently used clinically to treat urea cycle disorders under the trade name Buphenyl. Recent studies however have explored 4-PBA in the context of a low weight molecular weight chemical chaperone. Its properties as a chemical chaperone prevent misfolded protein aggregation and alleviate endoplasmic reticulum (ER) stress. As the ER is responsible for folding proteins targeted for use in membranes or secreted out of the cell, failure of maintaining adequate ER homeostasis may lead to protein misfolding and subsequent cell and organ pathology. Accumulation of misfolded proteins within the ER activates the unfolded protein response (UPR), a molecular repair response. The activation of the UPR aims to restore ER and cellular proteostasis by regulating the rate of synthesis of newly formed proteins as well as initiating molecular programs aimed to help fold or degrade misfolded proteins. If proteostasis is not restored, the UPR may initiate pro-apoptotic pathways. It is suggested that 4-PBA may help fold proteins in the ER, attenuating the activation of the UPR, and thus potentially alleviating various pathologies. This review discusses the biomedical research exploring the potential therapeutic effects of 4-PBA in various in vitro and in vivo model systems and clinical trials, while also commenting on the possible mechanisms of action.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>25660369</pmid><doi>10.1016/j.biocel.2015.01.015</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-0202-735X</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1357-2725 |
ispartof | The international journal of biochemistry & cell biology, 2015-04, Vol.61, p.45-52 |
issn | 1357-2725 1878-5875 |
language | eng |
recordid | cdi_proquest_miscellaneous_1677885172 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | 4-PBA 4-Phenylbutyric acid Animals Endoplasmic Reticulum - drug effects Endoplasmic Reticulum - metabolism Endoplasmic Reticulum Stress - drug effects ER stress Homeostasis Humans Phenylbutyrates - pharmacology Phenylbutyrates - therapeutic use Signal Transduction Unfolded Protein Response - drug effects UPR Urea Cycle Disorders, Inborn - drug therapy |
title | The therapeutic effects of 4-phenylbutyric acid in maintaining proteostasis |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T10%3A19%3A15IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20therapeutic%20effects%20of%204-phenylbutyric%20acid%20in%20maintaining%20proteostasis&rft.jtitle=The%20international%20journal%20of%20biochemistry%20&%20cell%20biology&rft.au=Kolb,%20P.S.&rft.date=2015-04-01&rft.volume=61&rft.spage=45&rft.epage=52&rft.pages=45-52&rft.issn=1357-2725&rft.eissn=1878-5875&rft_id=info:doi/10.1016/j.biocel.2015.01.015&rft_dat=%3Cproquest_cross%3E1677885172%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1677885172&rft_id=info:pmid/25660369&rft_els_id=S1357272515000254&rfr_iscdi=true |