MicroRNA-203 functions as a tumor suppressor in basal cell carcinoma
Basal cell carcinoma (BCC) of the skin represents the most common malignancy in humans. MicroRNAs (miRNAs), small regulatory RNAs with pleiotropic function, are commonly misregulated in cancer. Here we identify miR-203, a miRNA abundantly and preferentially expressed in skin, to be downregulated in...
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creator | Sonkoly, E Lovén, J Xu, N Meisgen, F Wei, T Brodin, P Jaks, V Kasper, M Shimokawa, T Harada, M Heilborn, J Hedblad, M-A Hippe, A Grandér, D Homey, B Zaphiropoulos, P G Arsenian-Henriksson, M Ståhle, M Pivarcsi, A |
description | Basal cell carcinoma (BCC) of the skin represents the most common malignancy in humans. MicroRNAs (miRNAs), small regulatory RNAs with pleiotropic function, are commonly misregulated in cancer. Here we identify miR-203, a miRNA abundantly and preferentially expressed in skin, to be downregulated in BCCs. We show that activation of the Hedgehog (HH) pathway, critically involved in the pathogenesis of BCCs, as well as the EGFR/MEK/ERK/c-JUN signaling pathway suppresses miR-203. We identify c-JUN, a key effector of the HH pathway, as a novel direct target for miR-203
in vivo
. Further supporting the role of miR-203 as a tumor suppressor,
in vivo
delivery of miR-203 mimics in a BCC mouse model results in the reduction of tumor growth. Our results identify a regulatory circuit involving miR-203 and c-JUN, which provides functional control over basal cell proliferation and differentiation. We propose that miR-203 functions as a ‘
bona fide
’ tumor suppressor in BCC, whose suppressed expression contributes to oncogenic transformation via derepression of multiple stemness- and proliferation-related genes, and its overexpression could be of therapeutic value. |
doi_str_mv | 10.1038/oncsis.2012.3 |
format | Article |
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in vivo
. Further supporting the role of miR-203 as a tumor suppressor,
in vivo
delivery of miR-203 mimics in a BCC mouse model results in the reduction of tumor growth. Our results identify a regulatory circuit involving miR-203 and c-JUN, which provides functional control over basal cell proliferation and differentiation. We propose that miR-203 functions as a ‘
bona fide
’ tumor suppressor in BCC, whose suppressed expression contributes to oncogenic transformation via derepression of multiple stemness- and proliferation-related genes, and its overexpression could be of therapeutic value.</description><identifier>ISSN: 2157-9024</identifier><identifier>EISSN: 2157-9024</identifier><identifier>DOI: 10.1038/oncsis.2012.3</identifier><identifier>PMID: 23552555</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/337/384/331 ; 631/67/581 ; 692/420/755 ; 692/699/67/1813/1349 ; Apoptosis ; Cell Biology ; Human Genetics ; Internal Medicine ; Medicine ; Medicine & Public Health ; Oncology ; Original ; original-article</subject><ispartof>Oncogenesis (New York, NY), 2012-03, Vol.1 (3), p.e3-e3</ispartof><rights>The Author(s) 2012</rights><rights>Copyright Nature Publishing Group Mar 2012</rights><rights>Copyright © 2012 Macmillan Publishers Limited 2012 Macmillan Publishers Limited</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c628t-2c74bb7cb553f085101123dbbea6c8fd1e5c39c0df7554b5992daab375758b653</citedby><cites>FETCH-LOGICAL-c628t-2c74bb7cb553f085101123dbbea6c8fd1e5c39c0df7554b5992daab375758b653</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/PMC3412636/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3412636/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,550,723,776,780,860,881,27901,27902,41096,42165,51551,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23552555$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-421685$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:130495966$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Sonkoly, E</creatorcontrib><creatorcontrib>Lovén, J</creatorcontrib><creatorcontrib>Xu, N</creatorcontrib><creatorcontrib>Meisgen, F</creatorcontrib><creatorcontrib>Wei, T</creatorcontrib><creatorcontrib>Brodin, P</creatorcontrib><creatorcontrib>Jaks, V</creatorcontrib><creatorcontrib>Kasper, M</creatorcontrib><creatorcontrib>Shimokawa, T</creatorcontrib><creatorcontrib>Harada, M</creatorcontrib><creatorcontrib>Heilborn, J</creatorcontrib><creatorcontrib>Hedblad, M-A</creatorcontrib><creatorcontrib>Hippe, A</creatorcontrib><creatorcontrib>Grandér, D</creatorcontrib><creatorcontrib>Homey, B</creatorcontrib><creatorcontrib>Zaphiropoulos, P G</creatorcontrib><creatorcontrib>Arsenian-Henriksson, M</creatorcontrib><creatorcontrib>Ståhle, M</creatorcontrib><creatorcontrib>Pivarcsi, A</creatorcontrib><title>MicroRNA-203 functions as a tumor suppressor in basal cell carcinoma</title><title>Oncogenesis (New York, NY)</title><addtitle>Oncogenesis</addtitle><addtitle>Oncogenesis</addtitle><description>Basal cell carcinoma (BCC) of the skin represents the most common malignancy in humans. MicroRNAs (miRNAs), small regulatory RNAs with pleiotropic function, are commonly misregulated in cancer. Here we identify miR-203, a miRNA abundantly and preferentially expressed in skin, to be downregulated in BCCs. We show that activation of the Hedgehog (HH) pathway, critically involved in the pathogenesis of BCCs, as well as the EGFR/MEK/ERK/c-JUN signaling pathway suppresses miR-203. We identify c-JUN, a key effector of the HH pathway, as a novel direct target for miR-203
in vivo
. Further supporting the role of miR-203 as a tumor suppressor,
in vivo
delivery of miR-203 mimics in a BCC mouse model results in the reduction of tumor growth. Our results identify a regulatory circuit involving miR-203 and c-JUN, which provides functional control over basal cell proliferation and differentiation. We propose that miR-203 functions as a ‘
bona fide
’ tumor suppressor in BCC, whose suppressed expression contributes to oncogenic transformation via derepression of multiple stemness- and proliferation-related genes, and its overexpression could be of therapeutic value.</description><subject>631/337/384/331</subject><subject>631/67/581</subject><subject>692/420/755</subject><subject>692/699/67/1813/1349</subject><subject>Apoptosis</subject><subject>Cell Biology</subject><subject>Human Genetics</subject><subject>Internal Medicine</subject><subject>Medicine</subject><subject>Medicine & Public 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A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MicroRNA-203 functions as a tumor suppressor in basal cell carcinoma</atitle><jtitle>Oncogenesis (New York, NY)</jtitle><stitle>Oncogenesis</stitle><addtitle>Oncogenesis</addtitle><date>2012-03-12</date><risdate>2012</risdate><volume>1</volume><issue>3</issue><spage>e3</spage><epage>e3</epage><pages>e3-e3</pages><issn>2157-9024</issn><eissn>2157-9024</eissn><abstract>Basal cell carcinoma (BCC) of the skin represents the most common malignancy in humans. MicroRNAs (miRNAs), small regulatory RNAs with pleiotropic function, are commonly misregulated in cancer. Here we identify miR-203, a miRNA abundantly and preferentially expressed in skin, to be downregulated in BCCs. We show that activation of the Hedgehog (HH) pathway, critically involved in the pathogenesis of BCCs, as well as the EGFR/MEK/ERK/c-JUN signaling pathway suppresses miR-203. We identify c-JUN, a key effector of the HH pathway, as a novel direct target for miR-203
in vivo
. Further supporting the role of miR-203 as a tumor suppressor,
in vivo
delivery of miR-203 mimics in a BCC mouse model results in the reduction of tumor growth. Our results identify a regulatory circuit involving miR-203 and c-JUN, which provides functional control over basal cell proliferation and differentiation. We propose that miR-203 functions as a ‘
bona fide
’ tumor suppressor in BCC, whose suppressed expression contributes to oncogenic transformation via derepression of multiple stemness- and proliferation-related genes, and its overexpression could be of therapeutic value.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>23552555</pmid><doi>10.1038/oncsis.2012.3</doi><oa>free_for_read</oa></addata></record> |
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subjects | 631/337/384/331 631/67/581 692/420/755 692/699/67/1813/1349 Apoptosis Cell Biology Human Genetics Internal Medicine Medicine Medicine & Public Health Oncology Original original-article |
title | MicroRNA-203 functions as a tumor suppressor in basal cell carcinoma |
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