Altered expression of MLL methyltransferase family genes in breast cancer

The histone lysine methyltransferases contain a SET domain, which catalyzes the addition of methyl groups to specific lysine residues. The MLL family of genes encodes histone-modifying enzymes with histone 3-lysine 4 methyltransferase activity that can regulate gene transcription. The MLL family exi...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:International journal of oncology 2013-08, Vol.43 (2), p.653-660
Hauptverfasser: RABELLO, DORALINA DO AMARAL, DE MOURA, CAROLINA AMARO, DE ANDRADE, ROSANGELA VIEIRA, MOTOYAMA, ANDREA BARRETTO, SILVA, FABIO PITTELLA
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 660
container_issue 2
container_start_page 653
container_title International journal of oncology
container_volume 43
creator RABELLO, DORALINA DO AMARAL
DE MOURA, CAROLINA AMARO
DE ANDRADE, ROSANGELA VIEIRA
MOTOYAMA, ANDREA BARRETTO
SILVA, FABIO PITTELLA
description The histone lysine methyltransferases contain a SET domain, which catalyzes the addition of methyl groups to specific lysine residues. The MLL family of genes encodes histone-modifying enzymes with histone 3-lysine 4 methyltransferase activity that can regulate gene transcription. The MLL family exists in multi-protein complexes and has been implicated in a variety of processes including normal development and cell growth. Although some of the MLL family members have already been described to be involved in cancer, a clear relationship of these genes with breast cancer is not determined to date. In the present study, we used quantitative PCR to investigate the expression profile of all five MLL genes [MLL (ALL-1), MLL2, MLL3, MLL4 and MLL5] in 7 breast cancer cell lines, 8 breast tumors and adjacent non-tumor tissues and in 12 normal tissues. We observed a diminished expression of all five genes in the breast cancer cell lines when compared to normal breast tissue. We found a significantly decreased expression of MLL2 in the tumor samples compared to the non-tumor controls. In tumor samples, MLL5 also showed a clear suppression tendency. Among the normal tissues analyzed, all genes showed a markedly higher expression in skeletal muscle and brain. Although further studies are required to determine the exact role of these methyltransferases in cancer development, our results indicate that the suppression of MLL genes, especially MLL2 and 5, take part in modulating breast carcinogenesis. Our assessment of the MLL family gene expression patterns in a diverse set of breast cancer cell lines and in a multitude of tissue types and breast tumors should lead to increasingly detailed information on the involvement of these genes in cancer progression.
doi_str_mv 10.3892/ijo.2013.1981
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1932329307</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1932329307</sourcerecordid><originalsourceid>FETCH-LOGICAL-c392t-b624a40446f5fb707bc4a8c75df3a3f3936bf637b1c84f0c2cedab9b6ff38d853</originalsourceid><addsrcrecordid>eNo90L1LAzEYx_Egiq3V0VUCDk6pSZ5c7jKW4kvhxEXnkOQSvXIvNbmC_e-90topGT78HvgidMvoHArFH-t1P-eUwZypgp2hKcsVI1xwOB__lCkiBagJukppTSnPMsou0YRDngkAOUWrRTP46CvsfzfRp1T3He4DfitL3Prhe9cM0XQp-GiSx8G0dbPDX77zCdcdttGbNGBnOufjNboIpkn-5vjO0Ofz08fylZTvL6vloiQOFB-IlVwYQYWQIQs2p7l1whQuz6oABgIokDZIyC1zhQjUcecrY5WVIUBRFRnM0P1hdxP7n61Pg17329iNJzVTwIEroPmoyEG52KcUfdCbWLcm7jSjeh9Oj-H0Ppzehxv93XF1a1tfnfR_qRE8HEDamK6qqz6dzLhEBBDKCZUZwB8oK3Zc</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1932329307</pqid></control><display><type>article</type><title>Altered expression of MLL methyltransferase family genes in breast cancer</title><source>Spandidos Publications Journals</source><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Alma/SFX Local Collection</source><creator>RABELLO, DORALINA DO AMARAL ; DE MOURA, CAROLINA AMARO ; DE ANDRADE, ROSANGELA VIEIRA ; MOTOYAMA, ANDREA BARRETTO ; SILVA, FABIO PITTELLA</creator><creatorcontrib>RABELLO, DORALINA DO AMARAL ; DE MOURA, CAROLINA AMARO ; DE ANDRADE, ROSANGELA VIEIRA ; MOTOYAMA, ANDREA BARRETTO ; SILVA, FABIO PITTELLA</creatorcontrib><description>The histone lysine methyltransferases contain a SET domain, which catalyzes the addition of methyl groups to specific lysine residues. The MLL family of genes encodes histone-modifying enzymes with histone 3-lysine 4 methyltransferase activity that can regulate gene transcription. The MLL family exists in multi-protein complexes and has been implicated in a variety of processes including normal development and cell growth. Although some of the MLL family members have already been described to be involved in cancer, a clear relationship of these genes with breast cancer is not determined to date. In the present study, we used quantitative PCR to investigate the expression profile of all five MLL genes [MLL (ALL-1), MLL2, MLL3, MLL4 and MLL5] in 7 breast cancer cell lines, 8 breast tumors and adjacent non-tumor tissues and in 12 normal tissues. We observed a diminished expression of all five genes in the breast cancer cell lines when compared to normal breast tissue. We found a significantly decreased expression of MLL2 in the tumor samples compared to the non-tumor controls. In tumor samples, MLL5 also showed a clear suppression tendency. Among the normal tissues analyzed, all genes showed a markedly higher expression in skeletal muscle and brain. Although further studies are required to determine the exact role of these methyltransferases in cancer development, our results indicate that the suppression of MLL genes, especially MLL2 and 5, take part in modulating breast carcinogenesis. Our assessment of the MLL family gene expression patterns in a diverse set of breast cancer cell lines and in a multitude of tissue types and breast tumors should lead to increasingly detailed information on the involvement of these genes in cancer progression.</description><identifier>ISSN: 1019-6439</identifier><identifier>EISSN: 1791-2423</identifier><identifier>DOI: 10.3892/ijo.2013.1981</identifier><identifier>PMID: 23754336</identifier><language>eng</language><publisher>Greece: D.A. Spandidos</publisher><subject>Breast cancer ; Breast Neoplasms - genetics ; Breast Neoplasms - pathology ; Carcinogenesis - genetics ; Cell cycle ; Cell Line, Tumor ; Cell Proliferation ; Chromosomes ; Defects ; Deoxyribonucleic acid ; DNA ; DNA methylation ; DNA-Binding Proteins - genetics ; Enzymes ; Epigenetics ; Female ; Gene expression ; Gene Expression Regulation, Neoplastic ; gene expression. MLL (ALL-1), MLL2, MLL3, MLL4 and MLL5 ; Humans ; Insects ; Leukemia ; MCF-7 Cells ; Methyltransferases - genetics ; Neoplasm Proteins - genetics ; Proteins ; Roles ; Stem cells ; Studies ; Tumors</subject><ispartof>International journal of oncology, 2013-08, Vol.43 (2), p.653-660</ispartof><rights>Copyright © 2013, Spandidos Publications</rights><rights>Copyright Spandidos Publications UK Ltd. 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c392t-b624a40446f5fb707bc4a8c75df3a3f3936bf637b1c84f0c2cedab9b6ff38d853</citedby><cites>FETCH-LOGICAL-c392t-b624a40446f5fb707bc4a8c75df3a3f3936bf637b1c84f0c2cedab9b6ff38d853</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,5556,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23754336$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>RABELLO, DORALINA DO AMARAL</creatorcontrib><creatorcontrib>DE MOURA, CAROLINA AMARO</creatorcontrib><creatorcontrib>DE ANDRADE, ROSANGELA VIEIRA</creatorcontrib><creatorcontrib>MOTOYAMA, ANDREA BARRETTO</creatorcontrib><creatorcontrib>SILVA, FABIO PITTELLA</creatorcontrib><title>Altered expression of MLL methyltransferase family genes in breast cancer</title><title>International journal of oncology</title><addtitle>Int J Oncol</addtitle><description>The histone lysine methyltransferases contain a SET domain, which catalyzes the addition of methyl groups to specific lysine residues. The MLL family of genes encodes histone-modifying enzymes with histone 3-lysine 4 methyltransferase activity that can regulate gene transcription. The MLL family exists in multi-protein complexes and has been implicated in a variety of processes including normal development and cell growth. Although some of the MLL family members have already been described to be involved in cancer, a clear relationship of these genes with breast cancer is not determined to date. In the present study, we used quantitative PCR to investigate the expression profile of all five MLL genes [MLL (ALL-1), MLL2, MLL3, MLL4 and MLL5] in 7 breast cancer cell lines, 8 breast tumors and adjacent non-tumor tissues and in 12 normal tissues. We observed a diminished expression of all five genes in the breast cancer cell lines when compared to normal breast tissue. We found a significantly decreased expression of MLL2 in the tumor samples compared to the non-tumor controls. In tumor samples, MLL5 also showed a clear suppression tendency. Among the normal tissues analyzed, all genes showed a markedly higher expression in skeletal muscle and brain. Although further studies are required to determine the exact role of these methyltransferases in cancer development, our results indicate that the suppression of MLL genes, especially MLL2 and 5, take part in modulating breast carcinogenesis. Our assessment of the MLL family gene expression patterns in a diverse set of breast cancer cell lines and in a multitude of tissue types and breast tumors should lead to increasingly detailed information on the involvement of these genes in cancer progression.</description><subject>Breast cancer</subject><subject>Breast Neoplasms - genetics</subject><subject>Breast Neoplasms - pathology</subject><subject>Carcinogenesis - genetics</subject><subject>Cell cycle</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation</subject><subject>Chromosomes</subject><subject>Defects</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA methylation</subject><subject>DNA-Binding Proteins - genetics</subject><subject>Enzymes</subject><subject>Epigenetics</subject><subject>Female</subject><subject>Gene expression</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>gene expression. MLL (ALL-1), MLL2, MLL3, MLL4 and MLL5</subject><subject>Humans</subject><subject>Insects</subject><subject>Leukemia</subject><subject>MCF-7 Cells</subject><subject>Methyltransferases - genetics</subject><subject>Neoplasm Proteins - genetics</subject><subject>Proteins</subject><subject>Roles</subject><subject>Stem cells</subject><subject>Studies</subject><subject>Tumors</subject><issn>1019-6439</issn><issn>1791-2423</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNo90L1LAzEYx_Egiq3V0VUCDk6pSZ5c7jKW4kvhxEXnkOQSvXIvNbmC_e-90topGT78HvgidMvoHArFH-t1P-eUwZypgp2hKcsVI1xwOB__lCkiBagJukppTSnPMsou0YRDngkAOUWrRTP46CvsfzfRp1T3He4DfitL3Prhe9cM0XQp-GiSx8G0dbPDX77zCdcdttGbNGBnOufjNboIpkn-5vjO0Ofz08fylZTvL6vloiQOFB-IlVwYQYWQIQs2p7l1whQuz6oABgIokDZIyC1zhQjUcecrY5WVIUBRFRnM0P1hdxP7n61Pg17329iNJzVTwIEroPmoyEG52KcUfdCbWLcm7jSjeh9Oj-H0Ppzehxv93XF1a1tfnfR_qRE8HEDamK6qqz6dzLhEBBDKCZUZwB8oK3Zc</recordid><startdate>20130801</startdate><enddate>20130801</enddate><creator>RABELLO, DORALINA DO AMARAL</creator><creator>DE MOURA, CAROLINA AMARO</creator><creator>DE ANDRADE, ROSANGELA VIEIRA</creator><creator>MOTOYAMA, ANDREA BARRETTO</creator><creator>SILVA, FABIO PITTELLA</creator><general>D.A. Spandidos</general><general>Spandidos Publications UK Ltd</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>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20130801</creationdate><title>Altered expression of MLL methyltransferase family genes in breast cancer</title><author>RABELLO, DORALINA DO AMARAL ; DE MOURA, CAROLINA AMARO ; DE ANDRADE, ROSANGELA VIEIRA ; MOTOYAMA, ANDREA BARRETTO ; SILVA, FABIO PITTELLA</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c392t-b624a40446f5fb707bc4a8c75df3a3f3936bf637b1c84f0c2cedab9b6ff38d853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Breast cancer</topic><topic>Breast Neoplasms - genetics</topic><topic>Breast Neoplasms - pathology</topic><topic>Carcinogenesis - genetics</topic><topic>Cell cycle</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation</topic><topic>Chromosomes</topic><topic>Defects</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA methylation</topic><topic>DNA-Binding Proteins - genetics</topic><topic>Enzymes</topic><topic>Epigenetics</topic><topic>Female</topic><topic>Gene expression</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>gene expression. MLL (ALL-1), MLL2, MLL3, MLL4 and MLL5</topic><topic>Humans</topic><topic>Insects</topic><topic>Leukemia</topic><topic>MCF-7 Cells</topic><topic>Methyltransferases - genetics</topic><topic>Neoplasm Proteins - genetics</topic><topic>Proteins</topic><topic>Roles</topic><topic>Stem cells</topic><topic>Studies</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>RABELLO, DORALINA DO AMARAL</creatorcontrib><creatorcontrib>DE MOURA, CAROLINA AMARO</creatorcontrib><creatorcontrib>DE ANDRADE, ROSANGELA VIEIRA</creatorcontrib><creatorcontrib>MOTOYAMA, ANDREA BARRETTO</creatorcontrib><creatorcontrib>SILVA, FABIO PITTELLA</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>Medical Database (Alumni Edition)</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>British Nursing Database</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical 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><jtitle>International journal of oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>RABELLO, DORALINA DO AMARAL</au><au>DE MOURA, CAROLINA AMARO</au><au>DE ANDRADE, ROSANGELA VIEIRA</au><au>MOTOYAMA, ANDREA BARRETTO</au><au>SILVA, FABIO PITTELLA</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Altered expression of MLL methyltransferase family genes in breast cancer</atitle><jtitle>International journal of oncology</jtitle><addtitle>Int J Oncol</addtitle><date>2013-08-01</date><risdate>2013</risdate><volume>43</volume><issue>2</issue><spage>653</spage><epage>660</epage><pages>653-660</pages><issn>1019-6439</issn><eissn>1791-2423</eissn><abstract>The histone lysine methyltransferases contain a SET domain, which catalyzes the addition of methyl groups to specific lysine residues. The MLL family of genes encodes histone-modifying enzymes with histone 3-lysine 4 methyltransferase activity that can regulate gene transcription. The MLL family exists in multi-protein complexes and has been implicated in a variety of processes including normal development and cell growth. Although some of the MLL family members have already been described to be involved in cancer, a clear relationship of these genes with breast cancer is not determined to date. In the present study, we used quantitative PCR to investigate the expression profile of all five MLL genes [MLL (ALL-1), MLL2, MLL3, MLL4 and MLL5] in 7 breast cancer cell lines, 8 breast tumors and adjacent non-tumor tissues and in 12 normal tissues. We observed a diminished expression of all five genes in the breast cancer cell lines when compared to normal breast tissue. We found a significantly decreased expression of MLL2 in the tumor samples compared to the non-tumor controls. In tumor samples, MLL5 also showed a clear suppression tendency. Among the normal tissues analyzed, all genes showed a markedly higher expression in skeletal muscle and brain. Although further studies are required to determine the exact role of these methyltransferases in cancer development, our results indicate that the suppression of MLL genes, especially MLL2 and 5, take part in modulating breast carcinogenesis. Our assessment of the MLL family gene expression patterns in a diverse set of breast cancer cell lines and in a multitude of tissue types and breast tumors should lead to increasingly detailed information on the involvement of these genes in cancer progression.</abstract><cop>Greece</cop><pub>D.A. Spandidos</pub><pmid>23754336</pmid><doi>10.3892/ijo.2013.1981</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1019-6439
ispartof International journal of oncology, 2013-08, Vol.43 (2), p.653-660
issn 1019-6439
1791-2423
language eng
recordid cdi_proquest_journals_1932329307
source Spandidos Publications Journals; MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects Breast cancer
Breast Neoplasms - genetics
Breast Neoplasms - pathology
Carcinogenesis - genetics
Cell cycle
Cell Line, Tumor
Cell Proliferation
Chromosomes
Defects
Deoxyribonucleic acid
DNA
DNA methylation
DNA-Binding Proteins - genetics
Enzymes
Epigenetics
Female
Gene expression
Gene Expression Regulation, Neoplastic
gene expression. MLL (ALL-1), MLL2, MLL3, MLL4 and MLL5
Humans
Insects
Leukemia
MCF-7 Cells
Methyltransferases - genetics
Neoplasm Proteins - genetics
Proteins
Roles
Stem cells
Studies
Tumors
title Altered expression of MLL methyltransferase family genes in breast cancer
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T07%3A07%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Altered%20expression%20of%20MLL%20methyltransferase%20family%20genes%20in%20breast%20cancer&rft.jtitle=International%20journal%20of%20oncology&rft.au=RABELLO,%20DORALINA%20DO%20AMARAL&rft.date=2013-08-01&rft.volume=43&rft.issue=2&rft.spage=653&rft.epage=660&rft.pages=653-660&rft.issn=1019-6439&rft.eissn=1791-2423&rft_id=info:doi/10.3892/ijo.2013.1981&rft_dat=%3Cproquest_cross%3E1932329307%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1932329307&rft_id=info:pmid/23754336&rfr_iscdi=true