Wnt signalling and prostate cancer

The Wnt signalling pathway plays a role in the direction of embryological development and maintenance of stem cell populations. Heritable alterations in genes encoding molecules of the Wnt pathway, including mutation and epigenetic events, have been demonstrated in a variety of cancers. It has been...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Prostate cancer and prostatic diseases 2005-06, Vol.8 (2), p.119-126
Hauptverfasser: Yardy, G W, Brewster, S F
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 126
container_issue 2
container_start_page 119
container_title Prostate cancer and prostatic diseases
container_volume 8
creator Yardy, G W
Brewster, S F
description The Wnt signalling pathway plays a role in the direction of embryological development and maintenance of stem cell populations. Heritable alterations in genes encoding molecules of the Wnt pathway, including mutation and epigenetic events, have been demonstrated in a variety of cancers. It has been proposed that disruption of this pathway is a significant step in the development of many tumours. Interactions between β -catenin—the effector molecule of the Wnt pathway—and the androgen receptor highlight the pathway's relevance to urological malignancy. Mutation or altered expression of Wnt genes in tumours may give prognostic information and treatments are being developed which target this pathway.
doi_str_mv 10.1038/sj.pcan.4500794
format Article
fullrecord <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_67892860</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A189245890</galeid><sourcerecordid>A189245890</sourcerecordid><originalsourceid>FETCH-LOGICAL-c524t-15e1b0d37aae1a537038df5be1470bc8ff2fcec640e3202d019165a9477da2343</originalsourceid><addsrcrecordid>eNp1kc1PGzEQxa2KqnyUM6dWEZV62zD-Xh8RohQJqZcijpbjnQ0bbbzB9h7473G6KRFIyAdb9m_evPEj5IzCnAKvL9JqvvEuzIUE0EZ8IkdUaFVJBfVBOXMlK11LdkiOU1oBgKEGvpBDKmswSpkjcv4Q8ix1y-D6vgvLmQvNbBOHlF3GWVH2GL-Sz63rE57u9hNy_-v679Xv6u7Pze3V5V3lJRO5ohLpAhqunUPqJNfFX9PKBRZHsPB127LWo1cCkDNgDVBDlXRGaN04xgU_IT8n3dL_acSU7bpLHvveBRzGZJWuDasVFPDHO3A1jLFMkCxTQnLGqOaFOv-QYgak1mwLzSdo6Xq0XWiHHJ0vq8F154eAbVfuL2npLGRtYG_yX8Ejuj4_pqEfczeE9Ba8mEBffjNFbO0mdmsXny0Fu83OppXdZmd32ZWK7zvD42KNzZ7fhVUAmIBUnsIS436ijzW_TSXB5THiq-b_9xcIgquG</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>229057723</pqid></control><display><type>article</type><title>Wnt signalling and prostate cancer</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Yardy, G W ; Brewster, S F</creator><creatorcontrib>Yardy, G W ; Brewster, S F</creatorcontrib><description>The Wnt signalling pathway plays a role in the direction of embryological development and maintenance of stem cell populations. Heritable alterations in genes encoding molecules of the Wnt pathway, including mutation and epigenetic events, have been demonstrated in a variety of cancers. It has been proposed that disruption of this pathway is a significant step in the development of many tumours. Interactions between β -catenin—the effector molecule of the Wnt pathway—and the androgen receptor highlight the pathway's relevance to urological malignancy. Mutation or altered expression of Wnt genes in tumours may give prognostic information and treatments are being developed which target this pathway.</description><identifier>ISSN: 1365-7852</identifier><identifier>EISSN: 1476-5608</identifier><identifier>DOI: 10.1038/sj.pcan.4500794</identifier><identifier>PMID: 15809669</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Androgen receptors ; beta Catenin ; Biomedical and Life Sciences ; Biomedicine ; Cancer Research ; Cell Transformation, Neoplastic ; Cytoskeletal Proteins - physiology ; Epigenetics ; Gene expression ; Genes ; Humans ; Intercellular Signaling Peptides and Proteins - biosynthesis ; Intercellular Signaling Peptides and Proteins - genetics ; Intercellular Signaling Peptides and Proteins - physiology ; Male ; Malignancy ; Mutation ; Prognosis ; Prostate cancer ; Prostatic Neoplasms - genetics ; Prostatic Neoplasms - physiopathology ; Prostatic Neoplasms - therapy ; Protein-Tyrosine Kinases ; Receptors, Androgen - physiology ; review ; Signal Transduction ; Signaling ; Stem cells ; Trans-Activators - physiology ; Tumors ; Wnt protein ; Wnt Proteins ; β-Catenin</subject><ispartof>Prostate cancer and prostatic diseases, 2005-06, Vol.8 (2), p.119-126</ispartof><rights>Springer Nature Limited 2005</rights><rights>COPYRIGHT 2005 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Jun 2005</rights><rights>Nature Publishing Group 2005.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c524t-15e1b0d37aae1a537038df5be1470bc8ff2fcec640e3202d019165a9477da2343</citedby><cites>FETCH-LOGICAL-c524t-15e1b0d37aae1a537038df5be1470bc8ff2fcec640e3202d019165a9477da2343</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27926,27927</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15809669$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yardy, G W</creatorcontrib><creatorcontrib>Brewster, S F</creatorcontrib><title>Wnt signalling and prostate cancer</title><title>Prostate cancer and prostatic diseases</title><addtitle>Prostate Cancer Prostatic Dis</addtitle><addtitle>Prostate Cancer Prostatic Dis</addtitle><description>The Wnt signalling pathway plays a role in the direction of embryological development and maintenance of stem cell populations. Heritable alterations in genes encoding molecules of the Wnt pathway, including mutation and epigenetic events, have been demonstrated in a variety of cancers. It has been proposed that disruption of this pathway is a significant step in the development of many tumours. Interactions between β -catenin—the effector molecule of the Wnt pathway—and the androgen receptor highlight the pathway's relevance to urological malignancy. Mutation or altered expression of Wnt genes in tumours may give prognostic information and treatments are being developed which target this pathway.</description><subject>Androgen receptors</subject><subject>beta Catenin</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer Research</subject><subject>Cell Transformation, Neoplastic</subject><subject>Cytoskeletal Proteins - physiology</subject><subject>Epigenetics</subject><subject>Gene expression</subject><subject>Genes</subject><subject>Humans</subject><subject>Intercellular Signaling Peptides and Proteins - biosynthesis</subject><subject>Intercellular Signaling Peptides and Proteins - genetics</subject><subject>Intercellular Signaling Peptides and Proteins - physiology</subject><subject>Male</subject><subject>Malignancy</subject><subject>Mutation</subject><subject>Prognosis</subject><subject>Prostate cancer</subject><subject>Prostatic Neoplasms - genetics</subject><subject>Prostatic Neoplasms - physiopathology</subject><subject>Prostatic Neoplasms - therapy</subject><subject>Protein-Tyrosine Kinases</subject><subject>Receptors, Androgen - physiology</subject><subject>review</subject><subject>Signal Transduction</subject><subject>Signaling</subject><subject>Stem cells</subject><subject>Trans-Activators - physiology</subject><subject>Tumors</subject><subject>Wnt protein</subject><subject>Wnt Proteins</subject><subject>β-Catenin</subject><issn>1365-7852</issn><issn>1476-5608</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1kc1PGzEQxa2KqnyUM6dWEZV62zD-Xh8RohQJqZcijpbjnQ0bbbzB9h7473G6KRFIyAdb9m_evPEj5IzCnAKvL9JqvvEuzIUE0EZ8IkdUaFVJBfVBOXMlK11LdkiOU1oBgKEGvpBDKmswSpkjcv4Q8ix1y-D6vgvLmQvNbBOHlF3GWVH2GL-Sz63rE57u9hNy_-v679Xv6u7Pze3V5V3lJRO5ohLpAhqunUPqJNfFX9PKBRZHsPB127LWo1cCkDNgDVBDlXRGaN04xgU_IT8n3dL_acSU7bpLHvveBRzGZJWuDasVFPDHO3A1jLFMkCxTQnLGqOaFOv-QYgak1mwLzSdo6Xq0XWiHHJ0vq8F154eAbVfuL2npLGRtYG_yX8Ejuj4_pqEfczeE9Ba8mEBffjNFbO0mdmsXny0Fu83OppXdZmd32ZWK7zvD42KNzZ7fhVUAmIBUnsIS436ijzW_TSXB5THiq-b_9xcIgquG</recordid><startdate>20050601</startdate><enddate>20050601</enddate><creator>Yardy, G W</creator><creator>Brewster, S F</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</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>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>M7Z</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20050601</creationdate><title>Wnt signalling and prostate cancer</title><author>Yardy, G W ; Brewster, S F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c524t-15e1b0d37aae1a537038df5be1470bc8ff2fcec640e3202d019165a9477da2343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Androgen receptors</topic><topic>beta Catenin</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cancer Research</topic><topic>Cell Transformation, Neoplastic</topic><topic>Cytoskeletal Proteins - physiology</topic><topic>Epigenetics</topic><topic>Gene expression</topic><topic>Genes</topic><topic>Humans</topic><topic>Intercellular Signaling Peptides and Proteins - biosynthesis</topic><topic>Intercellular Signaling Peptides and Proteins - genetics</topic><topic>Intercellular Signaling Peptides and Proteins - physiology</topic><topic>Male</topic><topic>Malignancy</topic><topic>Mutation</topic><topic>Prognosis</topic><topic>Prostate cancer</topic><topic>Prostatic Neoplasms - genetics</topic><topic>Prostatic Neoplasms - physiopathology</topic><topic>Prostatic Neoplasms - therapy</topic><topic>Protein-Tyrosine Kinases</topic><topic>Receptors, Androgen - physiology</topic><topic>review</topic><topic>Signal Transduction</topic><topic>Signaling</topic><topic>Stem cells</topic><topic>Trans-Activators - physiology</topic><topic>Tumors</topic><topic>Wnt protein</topic><topic>Wnt Proteins</topic><topic>β-Catenin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yardy, G W</creatorcontrib><creatorcontrib>Brewster, S F</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Prostate cancer and prostatic diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yardy, G W</au><au>Brewster, S F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Wnt signalling and prostate cancer</atitle><jtitle>Prostate cancer and prostatic diseases</jtitle><stitle>Prostate Cancer Prostatic Dis</stitle><addtitle>Prostate Cancer Prostatic Dis</addtitle><date>2005-06-01</date><risdate>2005</risdate><volume>8</volume><issue>2</issue><spage>119</spage><epage>126</epage><pages>119-126</pages><issn>1365-7852</issn><eissn>1476-5608</eissn><abstract>The Wnt signalling pathway plays a role in the direction of embryological development and maintenance of stem cell populations. Heritable alterations in genes encoding molecules of the Wnt pathway, including mutation and epigenetic events, have been demonstrated in a variety of cancers. It has been proposed that disruption of this pathway is a significant step in the development of many tumours. Interactions between β -catenin—the effector molecule of the Wnt pathway—and the androgen receptor highlight the pathway's relevance to urological malignancy. Mutation or altered expression of Wnt genes in tumours may give prognostic information and treatments are being developed which target this pathway.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>15809669</pmid><doi>10.1038/sj.pcan.4500794</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1365-7852
ispartof Prostate cancer and prostatic diseases, 2005-06, Vol.8 (2), p.119-126
issn 1365-7852
1476-5608
language eng
recordid cdi_proquest_miscellaneous_67892860
source MEDLINE; EZB-FREE-00999 freely available EZB journals
subjects Androgen receptors
beta Catenin
Biomedical and Life Sciences
Biomedicine
Cancer Research
Cell Transformation, Neoplastic
Cytoskeletal Proteins - physiology
Epigenetics
Gene expression
Genes
Humans
Intercellular Signaling Peptides and Proteins - biosynthesis
Intercellular Signaling Peptides and Proteins - genetics
Intercellular Signaling Peptides and Proteins - physiology
Male
Malignancy
Mutation
Prognosis
Prostate cancer
Prostatic Neoplasms - genetics
Prostatic Neoplasms - physiopathology
Prostatic Neoplasms - therapy
Protein-Tyrosine Kinases
Receptors, Androgen - physiology
review
Signal Transduction
Signaling
Stem cells
Trans-Activators - physiology
Tumors
Wnt protein
Wnt Proteins
β-Catenin
title Wnt signalling and prostate cancer
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T07%3A11%3A45IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Wnt%20signalling%20and%20prostate%20cancer&rft.jtitle=Prostate%20cancer%20and%20prostatic%20diseases&rft.au=Yardy,%20G%20W&rft.date=2005-06-01&rft.volume=8&rft.issue=2&rft.spage=119&rft.epage=126&rft.pages=119-126&rft.issn=1365-7852&rft.eissn=1476-5608&rft_id=info:doi/10.1038/sj.pcan.4500794&rft_dat=%3Cgale_proqu%3EA189245890%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=229057723&rft_id=info:pmid/15809669&rft_galeid=A189245890&rfr_iscdi=true