Role of JMJD6 in Breast Tumourigenesis
Protein arginine methylation is a common post translational modification that regulates protein properties. This modification is carried out by a family of nine arginine methyltransferases (PRMTs). Arginine methylation has already been linked to tumourigenesis as overexpression of these enzymes was...
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creator | Poulard, Coralie Rambaud, Juliette Lavergne, Emilie Jacquemetton, Julien Renoir, Jack-Michel Trédan, Olivier Chabaud, Sylvie Treilleux, Isabelle Corbo, Laura Le Romancer, Muriel |
description | Protein arginine methylation is a common post translational modification that regulates protein properties. This modification is carried out by a family of nine arginine methyltransferases (PRMTs). Arginine methylation has already been linked to tumourigenesis as overexpression of these enzymes was associated with various cancers, notably in breast cancers. Since the Jumonji Domain Containing 6 protein (JMJD6) possesses an arginine demethylase activity able to remove the methyl mark, we wanted to assess its potential role in breast tumourigenesis.
The expression of the protein by tissue microarray immunohistochemical staining was performed on a cohort of 133 breast tumours. Using cell lines stably overexpressing or knocked down for JMJD6, we evaluated its role on cell proliferation, cell migration, colony formation and mice tumour xenografts.
The analysis of JMJD6 expression in a cohort of breast tumour samples indicates that JMJD6 was highly expressed in aggressive breast tumours. Moreover, high expression of JMJD6 was associated with poor disease-free survival of patients in this cohort. JMJD6 silencing in breast tumoural cells promotes certain characteristics of tumourigenesis including proliferation, migration in vitro, and tumour growth in vivo. These effects are dependent on its demethylase activity as an enzymatic dead mutant lost these properties.
Although JMJD6 displays anti-tumoral properties in cell lines, its expression in breast tumours may be a marker of poor prognosis, suggesting that its function could be altered in breast cancer. |
doi_str_mv | 10.1371/journal.pone.0126181 |
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The expression of the protein by tissue microarray immunohistochemical staining was performed on a cohort of 133 breast tumours. Using cell lines stably overexpressing or knocked down for JMJD6, we evaluated its role on cell proliferation, cell migration, colony formation and mice tumour xenografts.
The analysis of JMJD6 expression in a cohort of breast tumour samples indicates that JMJD6 was highly expressed in aggressive breast tumours. Moreover, high expression of JMJD6 was associated with poor disease-free survival of patients in this cohort. JMJD6 silencing in breast tumoural cells promotes certain characteristics of tumourigenesis including proliferation, migration in vitro, and tumour growth in vivo. These effects are dependent on its demethylase activity as an enzymatic dead mutant lost these properties.
Although JMJD6 displays anti-tumoral properties in cell lines, its expression in breast tumours may be a marker of poor prognosis, suggesting that its function could be altered in breast cancer.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0126181</identifier><identifier>PMID: 25951181</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animals ; Apoptosis ; Arginine ; Biotechnology ; Breast cancer ; Breast Neoplasms - pathology ; Cell adhesion & migration ; Cell Line, Tumor ; Cell migration ; Cell proliferation ; Cell survival ; Cellular proteins ; Development and progression ; Female ; Gene expression ; Gene Knockdown Techniques ; Genetic aspects ; Health aspects ; Humans ; Jumonji Domain-Containing Histone Demethylases - genetics ; Jumonji Domain-Containing Histone Demethylases - physiology ; Localization ; Medical prognosis ; Methylation ; Mice ; Mice, Nude ; Middle Aged ; Prognosis ; Properties ; Properties (attributes) ; Protein arrays ; Proteins ; Signal transduction ; Tumorigenesis ; Tumors ; Xenografts</subject><ispartof>PloS one, 2015-05, Vol.10 (5), p.e0126181-e0126181</ispartof><rights>COPYRIGHT 2015 Public Library of Science</rights><rights>2015 Poulard et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2015 Poulard et al 2015 Poulard et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-c37d6171cde1762ec0e0a1b47d2b4105bb35cefc47ddeff67317b022e9c1527f3</citedby><cites>FETCH-LOGICAL-c692t-c37d6171cde1762ec0e0a1b47d2b4105bb35cefc47ddeff67317b022e9c1527f3</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/PMC4423888/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4423888/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2102,2928,23866,27924,27925,53791,53793,79600,79601</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25951181$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Migliaccio, Antimo</contributor><creatorcontrib>Poulard, Coralie</creatorcontrib><creatorcontrib>Rambaud, Juliette</creatorcontrib><creatorcontrib>Lavergne, Emilie</creatorcontrib><creatorcontrib>Jacquemetton, Julien</creatorcontrib><creatorcontrib>Renoir, Jack-Michel</creatorcontrib><creatorcontrib>Trédan, Olivier</creatorcontrib><creatorcontrib>Chabaud, Sylvie</creatorcontrib><creatorcontrib>Treilleux, Isabelle</creatorcontrib><creatorcontrib>Corbo, Laura</creatorcontrib><creatorcontrib>Le Romancer, Muriel</creatorcontrib><title>Role of JMJD6 in Breast Tumourigenesis</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Protein arginine methylation is a common post translational modification that regulates protein properties. This modification is carried out by a family of nine arginine methyltransferases (PRMTs). Arginine methylation has already been linked to tumourigenesis as overexpression of these enzymes was associated with various cancers, notably in breast cancers. Since the Jumonji Domain Containing 6 protein (JMJD6) possesses an arginine demethylase activity able to remove the methyl mark, we wanted to assess its potential role in breast tumourigenesis.
The expression of the protein by tissue microarray immunohistochemical staining was performed on a cohort of 133 breast tumours. Using cell lines stably overexpressing or knocked down for JMJD6, we evaluated its role on cell proliferation, cell migration, colony formation and mice tumour xenografts.
The analysis of JMJD6 expression in a cohort of breast tumour samples indicates that JMJD6 was highly expressed in aggressive breast tumours. Moreover, high expression of JMJD6 was associated with poor disease-free survival of patients in this cohort. JMJD6 silencing in breast tumoural cells promotes certain characteristics of tumourigenesis including proliferation, migration in vitro, and tumour growth in vivo. These effects are dependent on its demethylase activity as an enzymatic dead mutant lost these properties.
Although JMJD6 displays anti-tumoral properties in cell lines, its expression in breast tumours may be a marker of poor prognosis, suggesting that its function could be altered in breast cancer.</description><subject>Animals</subject><subject>Apoptosis</subject><subject>Arginine</subject><subject>Biotechnology</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - pathology</subject><subject>Cell adhesion & migration</subject><subject>Cell Line, Tumor</subject><subject>Cell migration</subject><subject>Cell proliferation</subject><subject>Cell survival</subject><subject>Cellular proteins</subject><subject>Development and progression</subject><subject>Female</subject><subject>Gene expression</subject><subject>Gene Knockdown Techniques</subject><subject>Genetic aspects</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Jumonji Domain-Containing Histone Demethylases - genetics</subject><subject>Jumonji Domain-Containing Histone Demethylases - physiology</subject><subject>Localization</subject><subject>Medical prognosis</subject><subject>Methylation</subject><subject>Mice</subject><subject>Mice, Nude</subject><subject>Middle Aged</subject><subject>Prognosis</subject><subject>Properties</subject><subject>Properties (attributes)</subject><subject>Protein arrays</subject><subject>Proteins</subject><subject>Signal transduction</subject><subject>Tumorigenesis</subject><subject>Tumors</subject><subject>Xenografts</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</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><sourceid>DOA</sourceid><recordid>eNqNkl2L1DAUhoso7jr6D0QLwqIXM-arSXqzsK5fs6wsrKu3IU1POhnaZmxa0X9v6nSXqeyFhJBw8pz35CRvkjzHaIWpwG-3fuhaXa92voUVwoRjiR8kxzinZMkJog8P9kfJkxC2CGVUcv44OSJZnuHIHycn176G1Nv04svFe566Nn3XgQ59ejM0sYCroIXgwtPkkdV1gGfTuki-ffxwc_55eXn1aX1-drk0PCf90lBRciywKQELTsAgQBoXTJSkYBhlRUEzA9bEQAnWckGxKBAhkBucEWHpInm5193VPqipxaAwFzlDJJMiEus9UXq9VbvONbr7rbx26m_Ad5XSXe9MDUoSxEyRacYYZ7nguSC5BoslFDKzLI9ap1O1oWigNND2na5novOT1m1U5X8qxgiVUkaB15NA538MEHrVuGCgrnULfhjvLREWGZJjrVf_oPd3N1GVjg241vpY14yi6oxRRCklcS6S1T1UHCU0zkQ_WBfjs4Q3s4TI9PCrr_QQglp_vf5_9ur7nD05YDeg634TfD30zrdhDrI9aDofQgf27pExUqOdb19DjXZWk51j2ovDD7pLuvUv_QO5GewE</recordid><startdate>20150507</startdate><enddate>20150507</enddate><creator>Poulard, 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of JMJD6 in Breast Tumourigenesis</title><author>Poulard, Coralie ; Rambaud, Juliette ; Lavergne, Emilie ; Jacquemetton, Julien ; Renoir, Jack-Michel ; Trédan, Olivier ; Chabaud, Sylvie ; Treilleux, Isabelle ; Corbo, Laura ; Le Romancer, Muriel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-c37d6171cde1762ec0e0a1b47d2b4105bb35cefc47ddeff67317b022e9c1527f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Apoptosis</topic><topic>Arginine</topic><topic>Biotechnology</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - pathology</topic><topic>Cell adhesion & migration</topic><topic>Cell Line, Tumor</topic><topic>Cell migration</topic><topic>Cell proliferation</topic><topic>Cell survival</topic><topic>Cellular proteins</topic><topic>Development and progression</topic><topic>Female</topic><topic>Gene expression</topic><topic>Gene Knockdown 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Juliette</au><au>Lavergne, Emilie</au><au>Jacquemetton, Julien</au><au>Renoir, Jack-Michel</au><au>Trédan, Olivier</au><au>Chabaud, Sylvie</au><au>Treilleux, Isabelle</au><au>Corbo, Laura</au><au>Le Romancer, Muriel</au><au>Migliaccio, Antimo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Role of JMJD6 in Breast Tumourigenesis</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2015-05-07</date><risdate>2015</risdate><volume>10</volume><issue>5</issue><spage>e0126181</spage><epage>e0126181</epage><pages>e0126181-e0126181</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Protein arginine methylation is a common post translational modification that regulates protein properties. This modification is carried out by a family of nine arginine methyltransferases (PRMTs). Arginine methylation has already been linked to tumourigenesis as overexpression of these enzymes was associated with various cancers, notably in breast cancers. Since the Jumonji Domain Containing 6 protein (JMJD6) possesses an arginine demethylase activity able to remove the methyl mark, we wanted to assess its potential role in breast tumourigenesis.
The expression of the protein by tissue microarray immunohistochemical staining was performed on a cohort of 133 breast tumours. Using cell lines stably overexpressing or knocked down for JMJD6, we evaluated its role on cell proliferation, cell migration, colony formation and mice tumour xenografts.
The analysis of JMJD6 expression in a cohort of breast tumour samples indicates that JMJD6 was highly expressed in aggressive breast tumours. Moreover, high expression of JMJD6 was associated with poor disease-free survival of patients in this cohort. JMJD6 silencing in breast tumoural cells promotes certain characteristics of tumourigenesis including proliferation, migration in vitro, and tumour growth in vivo. These effects are dependent on its demethylase activity as an enzymatic dead mutant lost these properties.
Although JMJD6 displays anti-tumoral properties in cell lines, its expression in breast tumours may be a marker of poor prognosis, suggesting that its function could be altered in breast cancer.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>25951181</pmid><doi>10.1371/journal.pone.0126181</doi><oa>free_for_read</oa></addata></record> |
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subjects | Animals Apoptosis Arginine Biotechnology Breast cancer Breast Neoplasms - pathology Cell adhesion & migration Cell Line, Tumor Cell migration Cell proliferation Cell survival Cellular proteins Development and progression Female Gene expression Gene Knockdown Techniques Genetic aspects Health aspects Humans Jumonji Domain-Containing Histone Demethylases - genetics Jumonji Domain-Containing Histone Demethylases - physiology Localization Medical prognosis Methylation Mice Mice, Nude Middle Aged Prognosis Properties Properties (attributes) Protein arrays Proteins Signal transduction Tumorigenesis Tumors Xenografts |
title | Role of JMJD6 in Breast Tumourigenesis |
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