Rational Design of Rho Protein Inhibitors
Rho GTPases are molecular switches that fluctuate between on and off states. When active, these proteins function to remodel the actin cytoskeleton by interacting with a number of downstream effector molecules. Recent studies have linked the activation of Rho GTPases with the acquisition of a metast...
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creator | Rojas, Rafael J |
description | Rho GTPases are molecular switches that fluctuate between on and off states. When active, these proteins function to remodel the actin cytoskeleton by interacting with a number of downstream effector molecules. Recent studies have linked the activation of Rho GTPases with the acquisition of a metastatic phenotype in many types of cancers especially breast cancer. This proposal incorporates a rational approach to target these signaling proteins using small molecule inhibitors that would interfere with their ability to become activated by Rho family guanine nucleotide exchange factors (RhoGEFs). We have developed a high throughput screening strategy identify novel inhibitors of Rho activation are currently following up on several compounds which appear to selectively inhibit Rho activation. These compounds may form the basis of future drug development strategies for the treatment of metastatic breast cancer. |
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When active, these proteins function to remodel the actin cytoskeleton by interacting with a number of downstream effector molecules. Recent studies have linked the activation of Rho GTPases with the acquisition of a metastatic phenotype in many types of cancers especially breast cancer. This proposal incorporates a rational approach to target these signaling proteins using small molecule inhibitors that would interfere with their ability to become activated by Rho family guanine nucleotide exchange factors (RhoGEFs). We have developed a high throughput screening strategy identify novel inhibitors of Rho activation are currently following up on several compounds which appear to selectively inhibit Rho activation. These compounds may form the basis of future drug development strategies for the treatment of metastatic breast cancer.</description><language>eng</language><subject>ACQUISITION ; ACTIVATION ; Anatomy and Physiology ; Biochemistry ; BREAST CANCER ; CELL STRUCTURE ; CYTOSKELETON ; DRUGS ; FIBERS ; FLUCTUATE ; FUNCTIONS ; HIGH RATE ; INHIBITORS ; METASTASIS ; MOLECULES ; MUSCLE PROTEINS ; PROTEINS ; RHO FAMILY GUANINE NUCLEOTIDE EXCHANGE FACTORS ; RHO GTPASES ; RHOGEF(RHO FAMILY GUANINE NUCLEOTIDE EXCHANGE FACTORS) ; SIGNALS ; STRATEGY ; SWITCHES ; TARGETS ; THROUGHPUT</subject><creationdate>2005</creationdate><rights>Approved for public release; distribution is unlimited.</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,780,885,27567,27568</link.rule.ids><linktorsrc>$$Uhttps://apps.dtic.mil/sti/citations/ADA446683$$EView_record_in_DTIC$$FView_record_in_$$GDTIC$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Rojas, Rafael J</creatorcontrib><creatorcontrib>NORTH CAROLINA UNIV AT CHAPEL HILL</creatorcontrib><title>Rational Design of Rho Protein Inhibitors</title><description>Rho GTPases are molecular switches that fluctuate between on and off states. When active, these proteins function to remodel the actin cytoskeleton by interacting with a number of downstream effector molecules. Recent studies have linked the activation of Rho GTPases with the acquisition of a metastatic phenotype in many types of cancers especially breast cancer. This proposal incorporates a rational approach to target these signaling proteins using small molecule inhibitors that would interfere with their ability to become activated by Rho family guanine nucleotide exchange factors (RhoGEFs). We have developed a high throughput screening strategy identify novel inhibitors of Rho activation are currently following up on several compounds which appear to selectively inhibit Rho activation. These compounds may form the basis of future drug development strategies for the treatment of metastatic breast cancer.</description><subject>ACQUISITION</subject><subject>ACTIVATION</subject><subject>Anatomy and Physiology</subject><subject>Biochemistry</subject><subject>BREAST CANCER</subject><subject>CELL STRUCTURE</subject><subject>CYTOSKELETON</subject><subject>DRUGS</subject><subject>FIBERS</subject><subject>FLUCTUATE</subject><subject>FUNCTIONS</subject><subject>HIGH RATE</subject><subject>INHIBITORS</subject><subject>METASTASIS</subject><subject>MOLECULES</subject><subject>MUSCLE PROTEINS</subject><subject>PROTEINS</subject><subject>RHO FAMILY GUANINE NUCLEOTIDE EXCHANGE FACTORS</subject><subject>RHO GTPASES</subject><subject>RHOGEF(RHO FAMILY GUANINE NUCLEOTIDE EXCHANGE FACTORS)</subject><subject>SIGNALS</subject><subject>STRATEGY</subject><subject>SWITCHES</subject><subject>TARGETS</subject><subject>THROUGHPUT</subject><fulltext>true</fulltext><rsrctype>report</rsrctype><creationdate>2005</creationdate><recordtype>report</recordtype><sourceid>1RU</sourceid><recordid>eNrjZNAMSizJzM9LzFFwSS3OTM9TyE9TCMrIVwgoyi9JzcxT8MzLyEzKLMkvKuZhYE1LzClO5YXS3Awybq4hzh66KSWZyfHFJZl5qSXxji6OJiZmZhbGxgSkAUJeJXg</recordid><startdate>200509</startdate><enddate>200509</enddate><creator>Rojas, Rafael J</creator><scope>1RU</scope><scope>BHM</scope></search><sort><creationdate>200509</creationdate><title>Rational Design of Rho Protein Inhibitors</title><author>Rojas, Rafael J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-dtic_stinet_ADA4466833</frbrgroupid><rsrctype>reports</rsrctype><prefilter>reports</prefilter><language>eng</language><creationdate>2005</creationdate><topic>ACQUISITION</topic><topic>ACTIVATION</topic><topic>Anatomy and Physiology</topic><topic>Biochemistry</topic><topic>BREAST CANCER</topic><topic>CELL STRUCTURE</topic><topic>CYTOSKELETON</topic><topic>DRUGS</topic><topic>FIBERS</topic><topic>FLUCTUATE</topic><topic>FUNCTIONS</topic><topic>HIGH RATE</topic><topic>INHIBITORS</topic><topic>METASTASIS</topic><topic>MOLECULES</topic><topic>MUSCLE PROTEINS</topic><topic>PROTEINS</topic><topic>RHO FAMILY GUANINE NUCLEOTIDE EXCHANGE FACTORS</topic><topic>RHO GTPASES</topic><topic>RHOGEF(RHO FAMILY GUANINE NUCLEOTIDE EXCHANGE FACTORS)</topic><topic>SIGNALS</topic><topic>STRATEGY</topic><topic>SWITCHES</topic><topic>TARGETS</topic><topic>THROUGHPUT</topic><toplevel>online_resources</toplevel><creatorcontrib>Rojas, Rafael J</creatorcontrib><creatorcontrib>NORTH CAROLINA UNIV AT CHAPEL HILL</creatorcontrib><collection>DTIC Technical Reports</collection><collection>DTIC STINET</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Rojas, Rafael J</au><aucorp>NORTH CAROLINA UNIV AT CHAPEL HILL</aucorp><format>book</format><genre>unknown</genre><ristype>RPRT</ristype><btitle>Rational Design of Rho Protein Inhibitors</btitle><date>2005-09</date><risdate>2005</risdate><abstract>Rho GTPases are molecular switches that fluctuate between on and off states. When active, these proteins function to remodel the actin cytoskeleton by interacting with a number of downstream effector molecules. Recent studies have linked the activation of Rho GTPases with the acquisition of a metastatic phenotype in many types of cancers especially breast cancer. This proposal incorporates a rational approach to target these signaling proteins using small molecule inhibitors that would interfere with their ability to become activated by Rho family guanine nucleotide exchange factors (RhoGEFs). We have developed a high throughput screening strategy identify novel inhibitors of Rho activation are currently following up on several compounds which appear to selectively inhibit Rho activation. These compounds may form the basis of future drug development strategies for the treatment of metastatic breast cancer.</abstract><oa>free_for_read</oa></addata></record> |
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source | DTIC Technical Reports |
subjects | ACQUISITION ACTIVATION Anatomy and Physiology Biochemistry BREAST CANCER CELL STRUCTURE CYTOSKELETON DRUGS FIBERS FLUCTUATE FUNCTIONS HIGH RATE INHIBITORS METASTASIS MOLECULES MUSCLE PROTEINS PROTEINS RHO FAMILY GUANINE NUCLEOTIDE EXCHANGE FACTORS RHO GTPASES RHOGEF(RHO FAMILY GUANINE NUCLEOTIDE EXCHANGE FACTORS) SIGNALS STRATEGY SWITCHES TARGETS THROUGHPUT |
title | Rational Design of Rho Protein Inhibitors |
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