miR-181a shows tumor suppressive effect against oral squamous cell carcinoma cells by downregulating K-ras

► MicroRNA-181a (miR-181a) was frequently downregulated in oral squamous cell carcinoma (OSCC). ► Overexpression of miR-181a suppressed OSCC growth. ► K-ras is a novel target of miR-181a. ► Decreased miR-181a expression is attributed to its lower promoter activity in OSCC. MicroRNAs (miRNAs) are epi...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Biochemical and biophysical research communications 2011-01, Vol.404 (4), p.896-902
Hauptverfasser: Shin, Ki-Hyuk, Bae, Susan D., Hong, Hannah S., Kim, Reuben H., Kang, Mo K., Park, No-Hee
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 902
container_issue 4
container_start_page 896
container_title Biochemical and biophysical research communications
container_volume 404
creator Shin, Ki-Hyuk
Bae, Susan D.
Hong, Hannah S.
Kim, Reuben H.
Kang, Mo K.
Park, No-Hee
description ► MicroRNA-181a (miR-181a) was frequently downregulated in oral squamous cell carcinoma (OSCC). ► Overexpression of miR-181a suppressed OSCC growth. ► K-ras is a novel target of miR-181a. ► Decreased miR-181a expression is attributed to its lower promoter activity in OSCC. MicroRNAs (miRNAs) are epigenetic regulators of gene expression, and their deregulation plays an important role in human cancer, including oral squamous cell carcinoma (OSCC). Recently, we found that miRNA-181a (miR-181a) was upregulated during replicative senescence of normal human oral keratinocytes. Since senescence is considered as a tumor suppressive mechanism, we thus investigated the expression and biological role of miR-181a in OSCC. We found that miR-181a was frequently downregulated in OSCC. Ectopic expression of miR-181a suppressed proliferation and anchorage independent growth ability of OSCC. Moreover, miR-181a dramatically reduces the growth of OSCC on three dimensional organotypic raft culture. We also identified K-ras as a novel target of miR-181a. miR-181a decreased K-ras protein level as well as the luciferase activity of reporter vectors containing the 3′-untranslated region of K-ras gene. Finally, we defined a minimal regulatory region of miR-181a and found a positive correlation between its promoter activity and the level of miR-181a expression. In conclusion, miR-181a may function as an OSCC suppressor by targeting on K-ras oncogene. Thus, miR-181a should be considered for therapeutic application for OSCC.
doi_str_mv 10.1016/j.bbrc.2010.12.055
format Article
fullrecord <record><control><sourceid>proquest_osti_</sourceid><recordid>TN_cdi_osti_scitechconnect_22204768</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0006291X1002293X</els_id><sourcerecordid>907153947</sourcerecordid><originalsourceid>FETCH-LOGICAL-c481t-505dd3e8eb22541c8161d7571d928c5d20f18fe362a8326fa25943dd3661a25b3</originalsourceid><addsrcrecordid>eNqFkU9v1DAQxS0EokvhC3BAljhwyuKZJI4jcUFV-SMqISGQuFmOM9l6tYm3nqRVvz0OWzjCyWPr95785gnxEtQWFOi3-23XJb9FtT7gVtX1I7EB1aoCQVWPxUYppQts4eeZeMa8Vwqg0u1TcYYAuoESN2I_hm8FGHCSr-Mdy3kZY5K8HI-JmMMtSRoG8rN0OxcmnmVM7iD5ZnFjXFh6Ohykd8mHKY7u95Vldy_7eDcl2i0HN4dpJ78UyfFz8WRwB6YXD-e5-PHh8vvFp-Lq68fPF--vCl8ZmIta1X1fkqEOsa7AG9DQN3UDfYvG1z2qAcxApUZnStSDw7qtyizRGvLclefi9ck38hws-zCTv_ZxmnIMi4iqarTJ1JsTdUzxZiGe7Rh4_b-bKCezrWqgLtuq-S9pKqNNAy1mEk-kT5E50WCPKYwu3VtQdq3M7u1amV0rs4A2V5ZFrx7sl26k_q_kT0cZeHcCKC_tNlBaM9HkqQ9pjdTH8C__X7MXppQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>848687192</pqid></control><display><type>article</type><title>miR-181a shows tumor suppressive effect against oral squamous cell carcinoma cells by downregulating K-ras</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Shin, Ki-Hyuk ; Bae, Susan D. ; Hong, Hannah S. ; Kim, Reuben H. ; Kang, Mo K. ; Park, No-Hee</creator><creatorcontrib>Shin, Ki-Hyuk ; Bae, Susan D. ; Hong, Hannah S. ; Kim, Reuben H. ; Kang, Mo K. ; Park, No-Hee</creatorcontrib><description>► MicroRNA-181a (miR-181a) was frequently downregulated in oral squamous cell carcinoma (OSCC). ► Overexpression of miR-181a suppressed OSCC growth. ► K-ras is a novel target of miR-181a. ► Decreased miR-181a expression is attributed to its lower promoter activity in OSCC. MicroRNAs (miRNAs) are epigenetic regulators of gene expression, and their deregulation plays an important role in human cancer, including oral squamous cell carcinoma (OSCC). Recently, we found that miRNA-181a (miR-181a) was upregulated during replicative senescence of normal human oral keratinocytes. Since senescence is considered as a tumor suppressive mechanism, we thus investigated the expression and biological role of miR-181a in OSCC. We found that miR-181a was frequently downregulated in OSCC. Ectopic expression of miR-181a suppressed proliferation and anchorage independent growth ability of OSCC. Moreover, miR-181a dramatically reduces the growth of OSCC on three dimensional organotypic raft culture. We also identified K-ras as a novel target of miR-181a. miR-181a decreased K-ras protein level as well as the luciferase activity of reporter vectors containing the 3′-untranslated region of K-ras gene. Finally, we defined a minimal regulatory region of miR-181a and found a positive correlation between its promoter activity and the level of miR-181a expression. In conclusion, miR-181a may function as an OSCC suppressor by targeting on K-ras oncogene. Thus, miR-181a should be considered for therapeutic application for OSCC.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1016/j.bbrc.2010.12.055</identifier><identifier>PMID: 21167132</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>60 APPLIED LIFE SCIENCES ; Base Sequence ; Carcinoma, Squamous Cell - genetics ; Carcinoma, Squamous Cell - pathology ; CARCINOMAS ; Cell Line, Tumor ; CELL PROLIFERATION ; DEREGULATION ; Down-Regulation ; Gene Expression Regulation, Neoplastic ; Genes, ras ; Genes, Tumor Suppressor - physiology ; Humans ; K-ras ; LUCIFERASE ; MicroRNAs - genetics ; MicroRNAs - physiology ; miR-181a ; Mouth Neoplasms - genetics ; Mouth Neoplasms - pathology ; ONCOGENES ; Oral cancer ; Promoter Regions, Genetic ; PROMOTERS ; Tumor suppressor</subject><ispartof>Biochemical and biophysical research communications, 2011-01, Vol.404 (4), p.896-902</ispartof><rights>2010</rights><rights>Published by Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c481t-505dd3e8eb22541c8161d7571d928c5d20f18fe362a8326fa25943dd3661a25b3</citedby><cites>FETCH-LOGICAL-c481t-505dd3e8eb22541c8161d7571d928c5d20f18fe362a8326fa25943dd3661a25b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.bbrc.2010.12.055$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,315,782,786,887,3554,27933,27934,46004</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21167132$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/22204768$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Shin, Ki-Hyuk</creatorcontrib><creatorcontrib>Bae, Susan D.</creatorcontrib><creatorcontrib>Hong, Hannah S.</creatorcontrib><creatorcontrib>Kim, Reuben H.</creatorcontrib><creatorcontrib>Kang, Mo K.</creatorcontrib><creatorcontrib>Park, No-Hee</creatorcontrib><title>miR-181a shows tumor suppressive effect against oral squamous cell carcinoma cells by downregulating K-ras</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><description>► MicroRNA-181a (miR-181a) was frequently downregulated in oral squamous cell carcinoma (OSCC). ► Overexpression of miR-181a suppressed OSCC growth. ► K-ras is a novel target of miR-181a. ► Decreased miR-181a expression is attributed to its lower promoter activity in OSCC. MicroRNAs (miRNAs) are epigenetic regulators of gene expression, and their deregulation plays an important role in human cancer, including oral squamous cell carcinoma (OSCC). Recently, we found that miRNA-181a (miR-181a) was upregulated during replicative senescence of normal human oral keratinocytes. Since senescence is considered as a tumor suppressive mechanism, we thus investigated the expression and biological role of miR-181a in OSCC. We found that miR-181a was frequently downregulated in OSCC. Ectopic expression of miR-181a suppressed proliferation and anchorage independent growth ability of OSCC. Moreover, miR-181a dramatically reduces the growth of OSCC on three dimensional organotypic raft culture. We also identified K-ras as a novel target of miR-181a. miR-181a decreased K-ras protein level as well as the luciferase activity of reporter vectors containing the 3′-untranslated region of K-ras gene. Finally, we defined a minimal regulatory region of miR-181a and found a positive correlation between its promoter activity and the level of miR-181a expression. In conclusion, miR-181a may function as an OSCC suppressor by targeting on K-ras oncogene. Thus, miR-181a should be considered for therapeutic application for OSCC.</description><subject>60 APPLIED LIFE SCIENCES</subject><subject>Base Sequence</subject><subject>Carcinoma, Squamous Cell - genetics</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>CARCINOMAS</subject><subject>Cell Line, Tumor</subject><subject>CELL PROLIFERATION</subject><subject>DEREGULATION</subject><subject>Down-Regulation</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Genes, ras</subject><subject>Genes, Tumor Suppressor - physiology</subject><subject>Humans</subject><subject>K-ras</subject><subject>LUCIFERASE</subject><subject>MicroRNAs - genetics</subject><subject>MicroRNAs - physiology</subject><subject>miR-181a</subject><subject>Mouth Neoplasms - genetics</subject><subject>Mouth Neoplasms - pathology</subject><subject>ONCOGENES</subject><subject>Oral cancer</subject><subject>Promoter Regions, Genetic</subject><subject>PROMOTERS</subject><subject>Tumor suppressor</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU9v1DAQxS0EokvhC3BAljhwyuKZJI4jcUFV-SMqISGQuFmOM9l6tYm3nqRVvz0OWzjCyWPr95785gnxEtQWFOi3-23XJb9FtT7gVtX1I7EB1aoCQVWPxUYppQts4eeZeMa8Vwqg0u1TcYYAuoESN2I_hm8FGHCSr-Mdy3kZY5K8HI-JmMMtSRoG8rN0OxcmnmVM7iD5ZnFjXFh6Ohykd8mHKY7u95Vldy_7eDcl2i0HN4dpJ78UyfFz8WRwB6YXD-e5-PHh8vvFp-Lq68fPF--vCl8ZmIta1X1fkqEOsa7AG9DQN3UDfYvG1z2qAcxApUZnStSDw7qtyizRGvLclefi9ck38hws-zCTv_ZxmnIMi4iqarTJ1JsTdUzxZiGe7Rh4_b-bKCezrWqgLtuq-S9pKqNNAy1mEk-kT5E50WCPKYwu3VtQdq3M7u1amV0rs4A2V5ZFrx7sl26k_q_kT0cZeHcCKC_tNlBaM9HkqQ9pjdTH8C__X7MXppQ</recordid><startdate>20110128</startdate><enddate>20110128</enddate><creator>Shin, Ki-Hyuk</creator><creator>Bae, Susan D.</creator><creator>Hong, Hannah S.</creator><creator>Kim, Reuben H.</creator><creator>Kang, Mo K.</creator><creator>Park, No-Hee</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>7TO</scope><scope>H94</scope><scope>OTOTI</scope></search><sort><creationdate>20110128</creationdate><title>miR-181a shows tumor suppressive effect against oral squamous cell carcinoma cells by downregulating K-ras</title><author>Shin, Ki-Hyuk ; Bae, Susan D. ; Hong, Hannah S. ; Kim, Reuben H. ; Kang, Mo K. ; Park, No-Hee</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c481t-505dd3e8eb22541c8161d7571d928c5d20f18fe362a8326fa25943dd3661a25b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>60 APPLIED LIFE SCIENCES</topic><topic>Base Sequence</topic><topic>Carcinoma, Squamous Cell - genetics</topic><topic>Carcinoma, Squamous Cell - pathology</topic><topic>CARCINOMAS</topic><topic>Cell Line, Tumor</topic><topic>CELL PROLIFERATION</topic><topic>DEREGULATION</topic><topic>Down-Regulation</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Genes, ras</topic><topic>Genes, Tumor Suppressor - physiology</topic><topic>Humans</topic><topic>K-ras</topic><topic>LUCIFERASE</topic><topic>MicroRNAs - genetics</topic><topic>MicroRNAs - physiology</topic><topic>miR-181a</topic><topic>Mouth Neoplasms - genetics</topic><topic>Mouth Neoplasms - pathology</topic><topic>ONCOGENES</topic><topic>Oral cancer</topic><topic>Promoter Regions, Genetic</topic><topic>PROMOTERS</topic><topic>Tumor suppressor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shin, Ki-Hyuk</creatorcontrib><creatorcontrib>Bae, Susan D.</creatorcontrib><creatorcontrib>Hong, Hannah S.</creatorcontrib><creatorcontrib>Kim, Reuben H.</creatorcontrib><creatorcontrib>Kang, Mo K.</creatorcontrib><creatorcontrib>Park, No-Hee</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>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>OSTI.GOV</collection><jtitle>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shin, Ki-Hyuk</au><au>Bae, Susan D.</au><au>Hong, Hannah S.</au><au>Kim, Reuben H.</au><au>Kang, Mo K.</au><au>Park, No-Hee</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>miR-181a shows tumor suppressive effect against oral squamous cell carcinoma cells by downregulating K-ras</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2011-01-28</date><risdate>2011</risdate><volume>404</volume><issue>4</issue><spage>896</spage><epage>902</epage><pages>896-902</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>► MicroRNA-181a (miR-181a) was frequently downregulated in oral squamous cell carcinoma (OSCC). ► Overexpression of miR-181a suppressed OSCC growth. ► K-ras is a novel target of miR-181a. ► Decreased miR-181a expression is attributed to its lower promoter activity in OSCC. MicroRNAs (miRNAs) are epigenetic regulators of gene expression, and their deregulation plays an important role in human cancer, including oral squamous cell carcinoma (OSCC). Recently, we found that miRNA-181a (miR-181a) was upregulated during replicative senescence of normal human oral keratinocytes. Since senescence is considered as a tumor suppressive mechanism, we thus investigated the expression and biological role of miR-181a in OSCC. We found that miR-181a was frequently downregulated in OSCC. Ectopic expression of miR-181a suppressed proliferation and anchorage independent growth ability of OSCC. Moreover, miR-181a dramatically reduces the growth of OSCC on three dimensional organotypic raft culture. We also identified K-ras as a novel target of miR-181a. miR-181a decreased K-ras protein level as well as the luciferase activity of reporter vectors containing the 3′-untranslated region of K-ras gene. Finally, we defined a minimal regulatory region of miR-181a and found a positive correlation between its promoter activity and the level of miR-181a expression. In conclusion, miR-181a may function as an OSCC suppressor by targeting on K-ras oncogene. Thus, miR-181a should be considered for therapeutic application for OSCC.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>21167132</pmid><doi>10.1016/j.bbrc.2010.12.055</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0006-291X
ispartof Biochemical and biophysical research communications, 2011-01, Vol.404 (4), p.896-902
issn 0006-291X
1090-2104
language eng
recordid cdi_osti_scitechconnect_22204768
source MEDLINE; Access via ScienceDirect (Elsevier)
subjects 60 APPLIED LIFE SCIENCES
Base Sequence
Carcinoma, Squamous Cell - genetics
Carcinoma, Squamous Cell - pathology
CARCINOMAS
Cell Line, Tumor
CELL PROLIFERATION
DEREGULATION
Down-Regulation
Gene Expression Regulation, Neoplastic
Genes, ras
Genes, Tumor Suppressor - physiology
Humans
K-ras
LUCIFERASE
MicroRNAs - genetics
MicroRNAs - physiology
miR-181a
Mouth Neoplasms - genetics
Mouth Neoplasms - pathology
ONCOGENES
Oral cancer
Promoter Regions, Genetic
PROMOTERS
Tumor suppressor
title miR-181a shows tumor suppressive effect against oral squamous cell carcinoma cells by downregulating K-ras
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-11-30T07%3A49%3A25IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_osti_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=miR-181a%20shows%20tumor%20suppressive%20effect%20against%20oral%20squamous%20cell%20carcinoma%20cells%20by%20downregulating%20K-ras&rft.jtitle=Biochemical%20and%20biophysical%20research%20communications&rft.au=Shin,%20Ki-Hyuk&rft.date=2011-01-28&rft.volume=404&rft.issue=4&rft.spage=896&rft.epage=902&rft.pages=896-902&rft.issn=0006-291X&rft.eissn=1090-2104&rft_id=info:doi/10.1016/j.bbrc.2010.12.055&rft_dat=%3Cproquest_osti_%3E907153947%3C/proquest_osti_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=848687192&rft_id=info:pmid/21167132&rft_els_id=S0006291X1002293X&rfr_iscdi=true