Druggable targets in the Rho pathway and their promise for therapeutic control of blood pressure
The prevalence of high blood pressure (also known as hypertension) has steadily increased over the last few decades. Known as a silent killer, hypertension increases the risk for cardiovascular disease and can lead to stroke, heart attack, kidney failure and associated sequela. While numerous hypert...
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Veröffentlicht in: | Pharmacology & therapeutics (Oxford) 2019-01, Vol.193, p.121-134 |
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description | The prevalence of high blood pressure (also known as hypertension) has steadily increased over the last few decades. Known as a silent killer, hypertension increases the risk for cardiovascular disease and can lead to stroke, heart attack, kidney failure and associated sequela. While numerous hypertensive therapies are currently available, it is estimated that only half of medicated patients exhibit blood pressure control. This signifies the need for a better understanding of the underlying cause of disease and for more effective therapies. While blood pressure homeostasis is very complex and involves the integrated control of multiple body systems, smooth muscle contractility and arterial resistance are important contributors. Strong evidence from pre-clinical animal models and genome-wide association studies indicate that smooth muscle contraction and BP homeostasis are governed by the small GTPase RhoA and its downstream target, Rho kinase. In this review, we summarize the signaling pathways and regulators that impart tight spatial-temporal control of RhoA activity in smooth muscle cells and discuss current therapeutic strategies to target these RhoA pathway components. We also discuss known allelic variations in the RhoA pathway and consider how these polymorphisms may affect genetic risk for hypertension and its clinical manifestations. |
doi_str_mv | 10.1016/j.pharmthera.2018.09.001 |
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Known as a silent killer, hypertension increases the risk for cardiovascular disease and can lead to stroke, heart attack, kidney failure and associated sequela. While numerous hypertensive therapies are currently available, it is estimated that only half of medicated patients exhibit blood pressure control. This signifies the need for a better understanding of the underlying cause of disease and for more effective therapies. While blood pressure homeostasis is very complex and involves the integrated control of multiple body systems, smooth muscle contractility and arterial resistance are important contributors. Strong evidence from pre-clinical animal models and genome-wide association studies indicate that smooth muscle contraction and BP homeostasis are governed by the small GTPase RhoA and its downstream target, Rho kinase. In this review, we summarize the signaling pathways and regulators that impart tight spatial-temporal control of RhoA activity in smooth muscle cells and discuss current therapeutic strategies to target these RhoA pathway components. We also discuss known allelic variations in the RhoA pathway and consider how these polymorphisms may affect genetic risk for hypertension and its clinical manifestations.</description><identifier>ISSN: 0163-7258</identifier><identifier>EISSN: 1879-016X</identifier><identifier>DOI: 10.1016/j.pharmthera.2018.09.001</identifier><identifier>PMID: 30189292</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>Animals ; Blood Pressure ; GTPase activating protein (GAP) ; GTPase-Activating Proteins - physiology ; Guanine nucleotide exchange factor (GEF) ; Humans ; Rho Kinase (ROCK) ; RhoA ; rhoA GTP-Binding Protein - physiology ; Signal Transduction ; Smooth muscle</subject><ispartof>Pharmacology & therapeutics (Oxford), 2019-01, Vol.193, p.121-134</ispartof><rights>2018 Elsevier Inc.</rights><rights>Copyright © 2018 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c479t-292f7e151a0b9b29166aa2157b20965afefcd28c04f8094a63358d21527564fa3</citedby><cites>FETCH-LOGICAL-c479t-292f7e151a0b9b29166aa2157b20965afefcd28c04f8094a63358d21527564fa3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.pharmthera.2018.09.001$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30189292$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dee, Rachel A.</creatorcontrib><creatorcontrib>Mangum, Kevin D.</creatorcontrib><creatorcontrib>Bai, Xue</creatorcontrib><creatorcontrib>Mack, Christopher P.</creatorcontrib><creatorcontrib>Taylor, Joan M.</creatorcontrib><title>Druggable targets in the Rho pathway and their promise for therapeutic control of blood pressure</title><title>Pharmacology & therapeutics (Oxford)</title><addtitle>Pharmacol Ther</addtitle><description>The prevalence of high blood pressure (also known as hypertension) has steadily increased over the last few decades. Known as a silent killer, hypertension increases the risk for cardiovascular disease and can lead to stroke, heart attack, kidney failure and associated sequela. While numerous hypertensive therapies are currently available, it is estimated that only half of medicated patients exhibit blood pressure control. This signifies the need for a better understanding of the underlying cause of disease and for more effective therapies. While blood pressure homeostasis is very complex and involves the integrated control of multiple body systems, smooth muscle contractility and arterial resistance are important contributors. Strong evidence from pre-clinical animal models and genome-wide association studies indicate that smooth muscle contraction and BP homeostasis are governed by the small GTPase RhoA and its downstream target, Rho kinase. In this review, we summarize the signaling pathways and regulators that impart tight spatial-temporal control of RhoA activity in smooth muscle cells and discuss current therapeutic strategies to target these RhoA pathway components. We also discuss known allelic variations in the RhoA pathway and consider how these polymorphisms may affect genetic risk for hypertension and its clinical manifestations.</description><subject>Animals</subject><subject>Blood Pressure</subject><subject>GTPase activating protein (GAP)</subject><subject>GTPase-Activating Proteins - physiology</subject><subject>Guanine nucleotide exchange factor (GEF)</subject><subject>Humans</subject><subject>Rho Kinase (ROCK)</subject><subject>RhoA</subject><subject>rhoA GTP-Binding Protein - physiology</subject><subject>Signal Transduction</subject><subject>Smooth muscle</subject><issn>0163-7258</issn><issn>1879-016X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtP3TAQha2Kqlxo_0LlJZuktvP0phKlDyohVUIgdedOnPGNr3Lj1Hao-Pf4cimPFauR7G_OnJlDCOUs54zXnzb5PIDfxgE95ILxNmcyZ4y_ISveNjJLzO8DskqlyBpRtYfkKIQNY6wsmXhHDovUIoUUK_Lnq1_Wa-hGpBH8GmOgdqJJmF4Ojs4Qh39wS2Hqd2_W09m7rQ1IjfP0fvyMS7SaajdF70bqDO1G5_oEYgiLx_fkrYEx4IeHekyuv3-7OjvPLn79-Hl2epHpspExS2ZMg7ziwDrZCcnrGkDwqukEk3UFBo3uRatZaVomS6iLomr7BIimqksDxTH5vNedl26LvcbkB0Y1e7sFf6scWPXyZ7KDWrsb1YiikmWbBE4eBLz7u2CIKi2qcRxhQrcEJdLlRS0bvkPbPaq9C8GjeRzDmdoFpDbqKSC1C0gxqVJAqfXjc5uPjf8TScCXPYDpWDcWvQra4qSxtx51VL2zr0-5A_UPqSw</recordid><startdate>20190101</startdate><enddate>20190101</enddate><creator>Dee, Rachel A.</creator><creator>Mangum, Kevin D.</creator><creator>Bai, Xue</creator><creator>Mack, Christopher P.</creator><creator>Taylor, Joan M.</creator><general>Elsevier Inc</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><scope>5PM</scope></search><sort><creationdate>20190101</creationdate><title>Druggable targets in the Rho pathway and their promise for therapeutic control of blood pressure</title><author>Dee, Rachel A. ; Mangum, Kevin D. ; Bai, Xue ; Mack, Christopher P. ; Taylor, Joan M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c479t-292f7e151a0b9b29166aa2157b20965afefcd28c04f8094a63358d21527564fa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animals</topic><topic>Blood Pressure</topic><topic>GTPase activating protein (GAP)</topic><topic>GTPase-Activating Proteins - physiology</topic><topic>Guanine nucleotide exchange factor (GEF)</topic><topic>Humans</topic><topic>Rho Kinase (ROCK)</topic><topic>RhoA</topic><topic>rhoA GTP-Binding Protein - physiology</topic><topic>Signal Transduction</topic><topic>Smooth muscle</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dee, Rachel A.</creatorcontrib><creatorcontrib>Mangum, Kevin D.</creatorcontrib><creatorcontrib>Bai, Xue</creatorcontrib><creatorcontrib>Mack, Christopher P.</creatorcontrib><creatorcontrib>Taylor, Joan M.</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Pharmacology & therapeutics (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dee, Rachel A.</au><au>Mangum, Kevin D.</au><au>Bai, Xue</au><au>Mack, Christopher P.</au><au>Taylor, Joan M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Druggable targets in the Rho pathway and their promise for therapeutic control of blood pressure</atitle><jtitle>Pharmacology & therapeutics (Oxford)</jtitle><addtitle>Pharmacol Ther</addtitle><date>2019-01-01</date><risdate>2019</risdate><volume>193</volume><spage>121</spage><epage>134</epage><pages>121-134</pages><issn>0163-7258</issn><eissn>1879-016X</eissn><abstract>The prevalence of high blood pressure (also known as hypertension) has steadily increased over the last few decades. Known as a silent killer, hypertension increases the risk for cardiovascular disease and can lead to stroke, heart attack, kidney failure and associated sequela. While numerous hypertensive therapies are currently available, it is estimated that only half of medicated patients exhibit blood pressure control. This signifies the need for a better understanding of the underlying cause of disease and for more effective therapies. While blood pressure homeostasis is very complex and involves the integrated control of multiple body systems, smooth muscle contractility and arterial resistance are important contributors. Strong evidence from pre-clinical animal models and genome-wide association studies indicate that smooth muscle contraction and BP homeostasis are governed by the small GTPase RhoA and its downstream target, Rho kinase. In this review, we summarize the signaling pathways and regulators that impart tight spatial-temporal control of RhoA activity in smooth muscle cells and discuss current therapeutic strategies to target these RhoA pathway components. We also discuss known allelic variations in the RhoA pathway and consider how these polymorphisms may affect genetic risk for hypertension and its clinical manifestations.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>30189292</pmid><doi>10.1016/j.pharmthera.2018.09.001</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Blood Pressure GTPase activating protein (GAP) GTPase-Activating Proteins - physiology Guanine nucleotide exchange factor (GEF) Humans Rho Kinase (ROCK) RhoA rhoA GTP-Binding Protein - physiology Signal Transduction Smooth muscle |
title | Druggable targets in the Rho pathway and their promise for therapeutic control of blood pressure |
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