Basal cell carcinoma - molecular biology and potential new therapies

Basal cell carcinoma (BCC) of the skin, the most common malignancy in individuals of mixed European descent, is increasing in incidence due to an aging population and sun exposure habits. The realization that aberrant activation of Hedgehog signaling is a pathognomonic feature of BCC development has...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The Journal of clinical investigation 2012-02, Vol.122 (2), p.455-463
Hauptverfasser: Kasper, Maria, Jaks, Viljar, Hohl, Daniel, Toftgård, Rune
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 463
container_issue 2
container_start_page 455
container_title The Journal of clinical investigation
container_volume 122
creator Kasper, Maria
Jaks, Viljar
Hohl, Daniel
Toftgård, Rune
description Basal cell carcinoma (BCC) of the skin, the most common malignancy in individuals of mixed European descent, is increasing in incidence due to an aging population and sun exposure habits. The realization that aberrant activation of Hedgehog signaling is a pathognomonic feature of BCC development has opened the way for exciting progress toward understanding BCC biology and translation of this knowledge to the clinic. Genetic mouse models closely mimicking human BCCs have provided answers about the tumor cell of origin, and inhibition of Hedgehog signaling is emerging as a potentially useful targeted therapy for patients with advanced or multiple BCCs that have hitherto lacked effective treatment.
doi_str_mv 10.1172/JCI58779
format Article
fullrecord <record><control><sourceid>proquest_swepu</sourceid><recordid>TN_cdi_swepub_primary_oai_swepub_ki_se_539278</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2586586811</sourcerecordid><originalsourceid>FETCH-LOGICAL-c486t-85eadcfbd0a25ca9e16cecfa3058900f30e61c31aa1fb389bb7b3b761f36b73c3</originalsourceid><addsrcrecordid>eNp1kU9P3DAQxa0KVLZQqZ8ARZx6CdieOLYvlcrSFtBKvZSzNXYcCM3GqZ0t2m-P0e7y58DFtjy_98bjR8gXRk8Zk_zsen4llJT6A5kxIVSpOKg9MqOUs1JLUAfkU0r3lLKqEtVHcsA518BUNSMX55iwL5zv84LRdUNYYlEWy9B7t-oxFrYLfbhdFzg0xRgmP0xdFgz-oZjufMSx8-mI7LfYJ_95ux-Sm58__swvy8XvX1fz74vSVaqeSiU8Nq61DUUuHGrPauddi0CF0pS2QH3NHDBE1lpQ2lppwcqatVBbCQ4OSbnxTQ9-XFkzxm6JcW0CdmZ79TefvBGguVSZ1-_yYwzNi2gnZBy0BqnrrP220WZg6RuX547Yv7V4Uxm6O3Mb_hvgdZ17Z4OTrUEM_1Y-TeY-rOKQ_8dozioFXIoMfd1ALoaUom-fGzBqnqI1u2gzevz6Qc_gLkt4BN_boRc</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>921483275</pqid></control><display><type>article</type><title>Basal cell carcinoma - molecular biology and potential new therapies</title><source>MEDLINE</source><source>SWEPUB Freely available online</source><source>Journals@Ovid Complete</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><creator>Kasper, Maria ; Jaks, Viljar ; Hohl, Daniel ; Toftgård, Rune</creator><creatorcontrib>Kasper, Maria ; Jaks, Viljar ; Hohl, Daniel ; Toftgård, Rune</creatorcontrib><description>Basal cell carcinoma (BCC) of the skin, the most common malignancy in individuals of mixed European descent, is increasing in incidence due to an aging population and sun exposure habits. The realization that aberrant activation of Hedgehog signaling is a pathognomonic feature of BCC development has opened the way for exciting progress toward understanding BCC biology and translation of this knowledge to the clinic. Genetic mouse models closely mimicking human BCCs have provided answers about the tumor cell of origin, and inhibition of Hedgehog signaling is emerging as a potentially useful targeted therapy for patients with advanced or multiple BCCs that have hitherto lacked effective treatment.</description><identifier>ISSN: 0021-9738</identifier><identifier>ISSN: 1558-8238</identifier><identifier>EISSN: 1558-8238</identifier><identifier>DOI: 10.1172/JCI58779</identifier><identifier>PMID: 22293184</identifier><language>eng</language><publisher>United States: American Society for Clinical Investigation</publisher><subject>Animals ; Biomedical research ; Cancer therapies ; Carcinoma, Basal Cell - etiology ; Carcinoma, Basal Cell - pathology ; Carcinoma, Basal Cell - physiopathology ; Carcinoma, Basal Cell - therapy ; Clinical Trials as Topic ; Disease Models, Animal ; Hedgehog Proteins - genetics ; Hedgehog Proteins - metabolism ; Humans ; Medicin och hälsovetenskap ; Molecular Biology ; Radiation ; Review Series ; Signal Transduction - physiology ; Skin - pathology ; Skin - radiation effects ; Skin Neoplasms - etiology ; Skin Neoplasms - pathology ; Skin Neoplasms - physiopathology ; Skin Neoplasms - therapy ; Tumors ; Ultraviolet Rays - adverse effects</subject><ispartof>The Journal of clinical investigation, 2012-02, Vol.122 (2), p.455-463</ispartof><rights>Copyright American Society for Clinical Investigation Feb 2012</rights><rights>Copyright © 2012, American Society for Clinical Investigation 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c486t-85eadcfbd0a25ca9e16cecfa3058900f30e61c31aa1fb389bb7b3b761f36b73c3</citedby><cites>FETCH-LOGICAL-c486t-85eadcfbd0a25ca9e16cecfa3058900f30e61c31aa1fb389bb7b3b761f36b73c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3266783/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3266783/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,552,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22293184$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:123993796$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Kasper, Maria</creatorcontrib><creatorcontrib>Jaks, Viljar</creatorcontrib><creatorcontrib>Hohl, Daniel</creatorcontrib><creatorcontrib>Toftgård, Rune</creatorcontrib><title>Basal cell carcinoma - molecular biology and potential new therapies</title><title>The Journal of clinical investigation</title><addtitle>J Clin Invest</addtitle><description>Basal cell carcinoma (BCC) of the skin, the most common malignancy in individuals of mixed European descent, is increasing in incidence due to an aging population and sun exposure habits. The realization that aberrant activation of Hedgehog signaling is a pathognomonic feature of BCC development has opened the way for exciting progress toward understanding BCC biology and translation of this knowledge to the clinic. Genetic mouse models closely mimicking human BCCs have provided answers about the tumor cell of origin, and inhibition of Hedgehog signaling is emerging as a potentially useful targeted therapy for patients with advanced or multiple BCCs that have hitherto lacked effective treatment.</description><subject>Animals</subject><subject>Biomedical research</subject><subject>Cancer therapies</subject><subject>Carcinoma, Basal Cell - etiology</subject><subject>Carcinoma, Basal Cell - pathology</subject><subject>Carcinoma, Basal Cell - physiopathology</subject><subject>Carcinoma, Basal Cell - therapy</subject><subject>Clinical Trials as Topic</subject><subject>Disease Models, Animal</subject><subject>Hedgehog Proteins - genetics</subject><subject>Hedgehog Proteins - metabolism</subject><subject>Humans</subject><subject>Medicin och hälsovetenskap</subject><subject>Molecular Biology</subject><subject>Radiation</subject><subject>Review Series</subject><subject>Signal Transduction - physiology</subject><subject>Skin - pathology</subject><subject>Skin - radiation effects</subject><subject>Skin Neoplasms - etiology</subject><subject>Skin Neoplasms - pathology</subject><subject>Skin Neoplasms - physiopathology</subject><subject>Skin Neoplasms - therapy</subject><subject>Tumors</subject><subject>Ultraviolet Rays - adverse effects</subject><issn>0021-9738</issn><issn>1558-8238</issn><issn>1558-8238</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>D8T</sourceid><recordid>eNp1kU9P3DAQxa0KVLZQqZ8ARZx6CdieOLYvlcrSFtBKvZSzNXYcCM3GqZ0t2m-P0e7y58DFtjy_98bjR8gXRk8Zk_zsen4llJT6A5kxIVSpOKg9MqOUs1JLUAfkU0r3lLKqEtVHcsA518BUNSMX55iwL5zv84LRdUNYYlEWy9B7t-oxFrYLfbhdFzg0xRgmP0xdFgz-oZjufMSx8-mI7LfYJ_95ux-Sm58__swvy8XvX1fz74vSVaqeSiU8Nq61DUUuHGrPauddi0CF0pS2QH3NHDBE1lpQ2lppwcqatVBbCQ4OSbnxTQ9-XFkzxm6JcW0CdmZ79TefvBGguVSZ1-_yYwzNi2gnZBy0BqnrrP220WZg6RuX547Yv7V4Uxm6O3Mb_hvgdZ17Z4OTrUEM_1Y-TeY-rOKQ_8dozioFXIoMfd1ALoaUom-fGzBqnqI1u2gzevz6Qc_gLkt4BN_boRc</recordid><startdate>20120201</startdate><enddate>20120201</enddate><creator>Kasper, Maria</creator><creator>Jaks, Viljar</creator><creator>Hohl, Daniel</creator><creator>Toftgård, Rune</creator><general>American Society for Clinical Investigation</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>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</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>BEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>S0X</scope><scope>5PM</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>ZZAVC</scope></search><sort><creationdate>20120201</creationdate><title>Basal cell carcinoma - molecular biology and potential new therapies</title><author>Kasper, Maria ; Jaks, Viljar ; Hohl, Daniel ; Toftgård, Rune</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c486t-85eadcfbd0a25ca9e16cecfa3058900f30e61c31aa1fb389bb7b3b761f36b73c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>Biomedical research</topic><topic>Cancer therapies</topic><topic>Carcinoma, Basal Cell - etiology</topic><topic>Carcinoma, Basal Cell - pathology</topic><topic>Carcinoma, Basal Cell - physiopathology</topic><topic>Carcinoma, Basal Cell - therapy</topic><topic>Clinical Trials as Topic</topic><topic>Disease Models, Animal</topic><topic>Hedgehog Proteins - genetics</topic><topic>Hedgehog Proteins - metabolism</topic><topic>Humans</topic><topic>Medicin och hälsovetenskap</topic><topic>Molecular Biology</topic><topic>Radiation</topic><topic>Review Series</topic><topic>Signal Transduction - physiology</topic><topic>Skin - pathology</topic><topic>Skin - radiation effects</topic><topic>Skin Neoplasms - etiology</topic><topic>Skin Neoplasms - pathology</topic><topic>Skin Neoplasms - physiopathology</topic><topic>Skin Neoplasms - therapy</topic><topic>Tumors</topic><topic>Ultraviolet Rays - adverse effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kasper, Maria</creatorcontrib><creatorcontrib>Jaks, Viljar</creatorcontrib><creatorcontrib>Hohl, Daniel</creatorcontrib><creatorcontrib>Toftgård, Rune</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>Nursing &amp; Allied Health Database</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</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>eLibrary</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</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>Nursing &amp; Allied Health Premium</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>SIRS Editorial</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SwePub Articles full text</collection><jtitle>The Journal of clinical investigation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kasper, Maria</au><au>Jaks, Viljar</au><au>Hohl, Daniel</au><au>Toftgård, Rune</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Basal cell carcinoma - molecular biology and potential new therapies</atitle><jtitle>The Journal of clinical investigation</jtitle><addtitle>J Clin Invest</addtitle><date>2012-02-01</date><risdate>2012</risdate><volume>122</volume><issue>2</issue><spage>455</spage><epage>463</epage><pages>455-463</pages><issn>0021-9738</issn><issn>1558-8238</issn><eissn>1558-8238</eissn><abstract>Basal cell carcinoma (BCC) of the skin, the most common malignancy in individuals of mixed European descent, is increasing in incidence due to an aging population and sun exposure habits. The realization that aberrant activation of Hedgehog signaling is a pathognomonic feature of BCC development has opened the way for exciting progress toward understanding BCC biology and translation of this knowledge to the clinic. Genetic mouse models closely mimicking human BCCs have provided answers about the tumor cell of origin, and inhibition of Hedgehog signaling is emerging as a potentially useful targeted therapy for patients with advanced or multiple BCCs that have hitherto lacked effective treatment.</abstract><cop>United States</cop><pub>American Society for Clinical Investigation</pub><pmid>22293184</pmid><doi>10.1172/JCI58779</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0021-9738
ispartof The Journal of clinical investigation, 2012-02, Vol.122 (2), p.455-463
issn 0021-9738
1558-8238
1558-8238
language eng
recordid cdi_swepub_primary_oai_swepub_ki_se_539278
source MEDLINE; SWEPUB Freely available online; Journals@Ovid Complete; EZB-FREE-00999 freely available EZB journals; PubMed Central; Alma/SFX Local Collection
subjects Animals
Biomedical research
Cancer therapies
Carcinoma, Basal Cell - etiology
Carcinoma, Basal Cell - pathology
Carcinoma, Basal Cell - physiopathology
Carcinoma, Basal Cell - therapy
Clinical Trials as Topic
Disease Models, Animal
Hedgehog Proteins - genetics
Hedgehog Proteins - metabolism
Humans
Medicin och hälsovetenskap
Molecular Biology
Radiation
Review Series
Signal Transduction - physiology
Skin - pathology
Skin - radiation effects
Skin Neoplasms - etiology
Skin Neoplasms - pathology
Skin Neoplasms - physiopathology
Skin Neoplasms - therapy
Tumors
Ultraviolet Rays - adverse effects
title Basal cell carcinoma - molecular biology and potential new therapies
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-23T01%3A29%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_swepu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Basal%20cell%20carcinoma%20-%20molecular%20biology%20and%20potential%20new%20therapies&rft.jtitle=The%20Journal%20of%20clinical%20investigation&rft.au=Kasper,%20Maria&rft.date=2012-02-01&rft.volume=122&rft.issue=2&rft.spage=455&rft.epage=463&rft.pages=455-463&rft.issn=0021-9738&rft.eissn=1558-8238&rft_id=info:doi/10.1172/JCI58779&rft_dat=%3Cproquest_swepu%3E2586586811%3C/proquest_swepu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=921483275&rft_id=info:pmid/22293184&rfr_iscdi=true