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...
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Veröffentlicht in: | International journal of oncology 2013-08, Vol.43 (2), p.653-660 |
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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 |
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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 & Allied Health Database</collection><collection>Health & 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 & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & 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> |
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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 |
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