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miR-98 suppresses melanoma metastasis through a negative feedback loop with its target gene IL-6
Dysregulated microRNA (miRNA) expression has a critical role in tumor development and metastasis. However, the mechanism by which miRNAs control melanoma metastasis is unknown. Here, we report reduced miR-98 expression in melanoma tissues with increasing tumor stage as well as metastasis; its expres...
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Published in: | Experimental & molecular medicine 2014-10, Vol.46 (10), p.e116-e116 |
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description | Dysregulated microRNA (miRNA) expression has a critical role in tumor development and metastasis. However, the mechanism by which miRNAs control melanoma metastasis is unknown. Here, we report reduced miR-98 expression in melanoma tissues with increasing tumor stage as well as metastasis; its expression is also negatively associated with melanoma patient survival. Furthermore, we demonstrate that miR-98 inhibits melanoma cell migration
in vitro
as well as metastatic tumor size
in vivo
. We also found that
IL-6
is a target gene of miR-98, and IL-6 represses miR-98 levels via the Stat3-NF-κB-lin28B pathway. In an
in vivo
melanoma model, we demonstrate that miR-98 reduces melanoma metastasis and increases survival in part by reducing IL-6 levels; it also decreases Stat3 and p65 phosphorylation as well as lin28B mRNA levels. These results suggest that miR-98 inhibits melanoma metastasis in part through a novel miR-98-
IL-6
-negative feedback loop.
Cancer: Small RNA molecule keeps melanoma in check
A short, non-coding RNA molecule called microRNA-98 inhibits the metastatic potential of melanoma skin cancer. A team in China led by Xiao-gang Wang of Jinan University and Wei Liu of the Air Force General Hospital of PLA analyzed levels of microRNA-98 in tissue biopsies taken from people with different stages of melanoma. They observed reduced expression of microRNA-98 in melanoma samples at a more advanced stage. Presence of the microRNA was also associated with lower patient survival. Laboratory experiments showed that microRNA-98 inhibited the migration potential of melanoma cells in a dish. It also reduced the size of metastatic tumors in mice, in part by suppressing levels of an immune signaling molecule called interleukin-6. Interleukin-6 promoted metastasis by repressing the activity of microRNA-98. |
doi_str_mv | 10.1038/emm.2014.63 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4221693</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1808630818</sourcerecordid><originalsourceid>FETCH-LOGICAL-c479t-a32112fd404060b34f026c5b322de1f8dd2aadd23aedd44da075cddda9f5ca183</originalsourceid><addsrcrecordid>eNqFkdtrFDEUxoMotlaffJeAL4LOmttkkhdBir3AgiD6HLOTM7OpM5MxyVT8781227KKUAgnB86P71w-hF5SsqKEq_cwjitGqFhJ_ggdM6JZJQXljw_yI_QspStCWC0a8RQdsZo1DaP0GH0f_ZdKK5yWeY6QEiQ8wmCnMNqSZJvK8wnnbQxLv8UWT9Db7K8BdwBuY9sfeAhhxr983mKfC2ljDxn3MAG-XFfyOXrS2SHBi9v_BH07-_T19KJafz6_PP24rlrR6FxZXsZhnRNEEEk2XHSEybbecMYc0E45x6wtgVtwTghnSVO3zjmru7q1VPET9GGvOy-bEVwLU452MHP0o42_TbDe_F2Z_Nb04doIxqjUvAi8uRWI4ecCKZvRpxaGcgwISzJUESU5UTe9HkBrJWlZRNGCvv4HvQpLnMolDG201oTqRhbq7Z5qY0gpQnc_NyVmZ7IpJpudyUbuJn11uOo9e-dqAd7tgVRKUw_xoOl_9P4AKUyx1g</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1799901976</pqid></control><display><type>article</type><title>miR-98 suppresses melanoma metastasis through a negative feedback loop with its target gene IL-6</title><source>Publicly Available Content Database</source><source>Full-Text Journals in Chemistry (Open access)</source><source>PubMed Central</source><source>Springer Nature - nature.com Journals - Fully Open Access</source><creator>Li, Fei ; Li, Xin-ji ; Qiao, Li ; Shi, Fei ; Liu, Wen ; Li, You ; Dang, Yu-ping ; Gu, Wei-jie ; Wang, Xiao-gang ; Liu, Wei</creator><creatorcontrib>Li, Fei ; Li, Xin-ji ; Qiao, Li ; Shi, Fei ; Liu, Wen ; Li, You ; Dang, Yu-ping ; Gu, Wei-jie ; Wang, Xiao-gang ; Liu, Wei</creatorcontrib><description>Dysregulated microRNA (miRNA) expression has a critical role in tumor development and metastasis. However, the mechanism by which miRNAs control melanoma metastasis is unknown. Here, we report reduced miR-98 expression in melanoma tissues with increasing tumor stage as well as metastasis; its expression is also negatively associated with melanoma patient survival. Furthermore, we demonstrate that miR-98 inhibits melanoma cell migration
in vitro
as well as metastatic tumor size
in vivo
. We also found that
IL-6
is a target gene of miR-98, and IL-6 represses miR-98 levels via the Stat3-NF-κB-lin28B pathway. In an
in vivo
melanoma model, we demonstrate that miR-98 reduces melanoma metastasis and increases survival in part by reducing IL-6 levels; it also decreases Stat3 and p65 phosphorylation as well as lin28B mRNA levels. These results suggest that miR-98 inhibits melanoma metastasis in part through a novel miR-98-
IL-6
-negative feedback loop.
Cancer: Small RNA molecule keeps melanoma in check
A short, non-coding RNA molecule called microRNA-98 inhibits the metastatic potential of melanoma skin cancer. A team in China led by Xiao-gang Wang of Jinan University and Wei Liu of the Air Force General Hospital of PLA analyzed levels of microRNA-98 in tissue biopsies taken from people with different stages of melanoma. They observed reduced expression of microRNA-98 in melanoma samples at a more advanced stage. Presence of the microRNA was also associated with lower patient survival. Laboratory experiments showed that microRNA-98 inhibited the migration potential of melanoma cells in a dish. It also reduced the size of metastatic tumors in mice, in part by suppressing levels of an immune signaling molecule called interleukin-6. Interleukin-6 promoted metastasis by repressing the activity of microRNA-98.</description><identifier>ISSN: 2092-6413</identifier><identifier>ISSN: 1226-3613</identifier><identifier>EISSN: 2092-6413</identifier><identifier>DOI: 10.1038/emm.2014.63</identifier><identifier>PMID: 25277211</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Animals ; Biomedical and Life Sciences ; Biomedicine ; Cell Line, Tumor ; Down-Regulation ; Gene Expression Regulation, Neoplastic ; Humans ; Interleukin-6 - genetics ; Male ; Medical Biochemistry ; Melanoma - epidemiology ; Melanoma - genetics ; Melanoma - pathology ; Mice ; Mice, Inbred C57BL ; MicroRNAs - genetics ; Molecular Medicine ; Neoplasm Metastasis - genetics ; Neoplasm Metastasis - pathology ; Original ; original-article ; Signal Transduction ; Stem Cells ; Survival Analysis</subject><ispartof>Experimental & molecular medicine, 2014-10, Vol.46 (10), p.e116-e116</ispartof><rights>The Author(s) 2014</rights><rights>Copyright Nature Publishing Group Oct 2014</rights><rights>Copyright © 2014 KSBMB. 2014 KSBMB.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c479t-a32112fd404060b34f026c5b322de1f8dd2aadd23aedd44da075cddda9f5ca183</citedby><cites>FETCH-LOGICAL-c479t-a32112fd404060b34f026c5b322de1f8dd2aadd23aedd44da075cddda9f5ca183</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1799901976/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1799901976?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25277211$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Fei</creatorcontrib><creatorcontrib>Li, Xin-ji</creatorcontrib><creatorcontrib>Qiao, Li</creatorcontrib><creatorcontrib>Shi, Fei</creatorcontrib><creatorcontrib>Liu, Wen</creatorcontrib><creatorcontrib>Li, You</creatorcontrib><creatorcontrib>Dang, Yu-ping</creatorcontrib><creatorcontrib>Gu, Wei-jie</creatorcontrib><creatorcontrib>Wang, Xiao-gang</creatorcontrib><creatorcontrib>Liu, Wei</creatorcontrib><title>miR-98 suppresses melanoma metastasis through a negative feedback loop with its target gene IL-6</title><title>Experimental & molecular medicine</title><addtitle>Exp Mol Med</addtitle><addtitle>Exp Mol Med</addtitle><description>Dysregulated microRNA (miRNA) expression has a critical role in tumor development and metastasis. However, the mechanism by which miRNAs control melanoma metastasis is unknown. Here, we report reduced miR-98 expression in melanoma tissues with increasing tumor stage as well as metastasis; its expression is also negatively associated with melanoma patient survival. Furthermore, we demonstrate that miR-98 inhibits melanoma cell migration
in vitro
as well as metastatic tumor size
in vivo
. We also found that
IL-6
is a target gene of miR-98, and IL-6 represses miR-98 levels via the Stat3-NF-κB-lin28B pathway. In an
in vivo
melanoma model, we demonstrate that miR-98 reduces melanoma metastasis and increases survival in part by reducing IL-6 levels; it also decreases Stat3 and p65 phosphorylation as well as lin28B mRNA levels. These results suggest that miR-98 inhibits melanoma metastasis in part through a novel miR-98-
IL-6
-negative feedback loop.
Cancer: Small RNA molecule keeps melanoma in check
A short, non-coding RNA molecule called microRNA-98 inhibits the metastatic potential of melanoma skin cancer. A team in China led by Xiao-gang Wang of Jinan University and Wei Liu of the Air Force General Hospital of PLA analyzed levels of microRNA-98 in tissue biopsies taken from people with different stages of melanoma. They observed reduced expression of microRNA-98 in melanoma samples at a more advanced stage. Presence of the microRNA was also associated with lower patient survival. Laboratory experiments showed that microRNA-98 inhibited the migration potential of melanoma cells in a dish. It also reduced the size of metastatic tumors in mice, in part by suppressing levels of an immune signaling molecule called interleukin-6. Interleukin-6 promoted metastasis by repressing the activity of microRNA-98.</description><subject>Animals</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cell Line, Tumor</subject><subject>Down-Regulation</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Humans</subject><subject>Interleukin-6 - genetics</subject><subject>Male</subject><subject>Medical Biochemistry</subject><subject>Melanoma - epidemiology</subject><subject>Melanoma - genetics</subject><subject>Melanoma - pathology</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>MicroRNAs - genetics</subject><subject>Molecular Medicine</subject><subject>Neoplasm Metastasis - genetics</subject><subject>Neoplasm Metastasis - pathology</subject><subject>Original</subject><subject>original-article</subject><subject>Signal Transduction</subject><subject>Stem Cells</subject><subject>Survival Analysis</subject><issn>2092-6413</issn><issn>1226-3613</issn><issn>2092-6413</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNqFkdtrFDEUxoMotlaffJeAL4LOmttkkhdBir3AgiD6HLOTM7OpM5MxyVT8781227KKUAgnB86P71w-hF5SsqKEq_cwjitGqFhJ_ggdM6JZJQXljw_yI_QspStCWC0a8RQdsZo1DaP0GH0f_ZdKK5yWeY6QEiQ8wmCnMNqSZJvK8wnnbQxLv8UWT9Db7K8BdwBuY9sfeAhhxr983mKfC2ljDxn3MAG-XFfyOXrS2SHBi9v_BH07-_T19KJafz6_PP24rlrR6FxZXsZhnRNEEEk2XHSEybbecMYc0E45x6wtgVtwTghnSVO3zjmru7q1VPET9GGvOy-bEVwLU452MHP0o42_TbDe_F2Z_Nb04doIxqjUvAi8uRWI4ecCKZvRpxaGcgwISzJUESU5UTe9HkBrJWlZRNGCvv4HvQpLnMolDG201oTqRhbq7Z5qY0gpQnc_NyVmZ7IpJpudyUbuJn11uOo9e-dqAd7tgVRKUw_xoOl_9P4AKUyx1g</recordid><startdate>20141001</startdate><enddate>20141001</enddate><creator>Li, Fei</creator><creator>Li, Xin-ji</creator><creator>Qiao, Li</creator><creator>Shi, Fei</creator><creator>Liu, Wen</creator><creator>Li, You</creator><creator>Dang, Yu-ping</creator><creator>Gu, Wei-jie</creator><creator>Wang, Xiao-gang</creator><creator>Liu, Wei</creator><general>Nature Publishing Group UK</general><general>Springer Nature B.V</general><general>Nature Publishing Group</general><scope>C6C</scope><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>7X7</scope><scope>7XB</scope><scope>88E</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>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>7T5</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope><scope>5PM</scope></search><sort><creationdate>20141001</creationdate><title>miR-98 suppresses melanoma metastasis through a negative feedback loop with its target gene IL-6</title><author>Li, Fei ; Li, Xin-ji ; Qiao, Li ; Shi, Fei ; Liu, Wen ; Li, You ; Dang, Yu-ping ; Gu, Wei-jie ; Wang, Xiao-gang ; Liu, Wei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c479t-a32112fd404060b34f026c5b322de1f8dd2aadd23aedd44da075cddda9f5ca183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cell Line, Tumor</topic><topic>Down-Regulation</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Humans</topic><topic>Interleukin-6 - genetics</topic><topic>Male</topic><topic>Medical Biochemistry</topic><topic>Melanoma - epidemiology</topic><topic>Melanoma - genetics</topic><topic>Melanoma - pathology</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>MicroRNAs - genetics</topic><topic>Molecular Medicine</topic><topic>Neoplasm Metastasis - genetics</topic><topic>Neoplasm Metastasis - pathology</topic><topic>Original</topic><topic>original-article</topic><topic>Signal Transduction</topic><topic>Stem Cells</topic><topic>Survival Analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Fei</creatorcontrib><creatorcontrib>Li, Xin-ji</creatorcontrib><creatorcontrib>Qiao, Li</creatorcontrib><creatorcontrib>Shi, Fei</creatorcontrib><creatorcontrib>Liu, Wen</creatorcontrib><creatorcontrib>Li, You</creatorcontrib><creatorcontrib>Dang, Yu-ping</creatorcontrib><creatorcontrib>Gu, Wei-jie</creatorcontrib><creatorcontrib>Wang, Xiao-gang</creatorcontrib><creatorcontrib>Liu, Wei</creatorcontrib><collection>SpringerOpen</collection><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>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</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)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</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 & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</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><collection>Immunology Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Experimental & molecular medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Fei</au><au>Li, Xin-ji</au><au>Qiao, Li</au><au>Shi, Fei</au><au>Liu, Wen</au><au>Li, You</au><au>Dang, Yu-ping</au><au>Gu, Wei-jie</au><au>Wang, Xiao-gang</au><au>Liu, Wei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>miR-98 suppresses melanoma metastasis through a negative feedback loop with its target gene IL-6</atitle><jtitle>Experimental & molecular medicine</jtitle><stitle>Exp Mol Med</stitle><addtitle>Exp Mol Med</addtitle><date>2014-10-01</date><risdate>2014</risdate><volume>46</volume><issue>10</issue><spage>e116</spage><epage>e116</epage><pages>e116-e116</pages><issn>2092-6413</issn><issn>1226-3613</issn><eissn>2092-6413</eissn><abstract>Dysregulated microRNA (miRNA) expression has a critical role in tumor development and metastasis. However, the mechanism by which miRNAs control melanoma metastasis is unknown. Here, we report reduced miR-98 expression in melanoma tissues with increasing tumor stage as well as metastasis; its expression is also negatively associated with melanoma patient survival. Furthermore, we demonstrate that miR-98 inhibits melanoma cell migration
in vitro
as well as metastatic tumor size
in vivo
. We also found that
IL-6
is a target gene of miR-98, and IL-6 represses miR-98 levels via the Stat3-NF-κB-lin28B pathway. In an
in vivo
melanoma model, we demonstrate that miR-98 reduces melanoma metastasis and increases survival in part by reducing IL-6 levels; it also decreases Stat3 and p65 phosphorylation as well as lin28B mRNA levels. These results suggest that miR-98 inhibits melanoma metastasis in part through a novel miR-98-
IL-6
-negative feedback loop.
Cancer: Small RNA molecule keeps melanoma in check
A short, non-coding RNA molecule called microRNA-98 inhibits the metastatic potential of melanoma skin cancer. A team in China led by Xiao-gang Wang of Jinan University and Wei Liu of the Air Force General Hospital of PLA analyzed levels of microRNA-98 in tissue biopsies taken from people with different stages of melanoma. They observed reduced expression of microRNA-98 in melanoma samples at a more advanced stage. Presence of the microRNA was also associated with lower patient survival. Laboratory experiments showed that microRNA-98 inhibited the migration potential of melanoma cells in a dish. It also reduced the size of metastatic tumors in mice, in part by suppressing levels of an immune signaling molecule called interleukin-6. Interleukin-6 promoted metastasis by repressing the activity of microRNA-98.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>25277211</pmid><doi>10.1038/emm.2014.63</doi><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biomedical and Life Sciences Biomedicine Cell Line, Tumor Down-Regulation Gene Expression Regulation, Neoplastic Humans Interleukin-6 - genetics Male Medical Biochemistry Melanoma - epidemiology Melanoma - genetics Melanoma - pathology Mice Mice, Inbred C57BL MicroRNAs - genetics Molecular Medicine Neoplasm Metastasis - genetics Neoplasm Metastasis - pathology Original original-article Signal Transduction Stem Cells Survival Analysis |
title | miR-98 suppresses melanoma metastasis through a negative feedback loop with its target gene IL-6 |
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