Expression profiling to predict postoperative prognosis for estrogen receptor‐negative breast cancers by analysis of 25,344 genes on a cDNA microarray
Estrogen receptor (ER) status is an essential determinant of clinical and biological behavior of human breast cancers. While ER‐positive breast cancers respond well to adjuvant hormone therapy, ER‐negative tumors are generally resistant. To date, no attempts have succeeded in finding molecular marke...
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Veröffentlicht in: | Cancer science 2004-03, Vol.95 (3), p.218-225 |
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creator | Nagahata, Takemitsu Onda, Masamitsu Emi, Mitsuru Nagai, Hisaki Tsumagari, Koji Fujimoto, Takashi Hirano, Akira Sato, Takamichi Nishikawa, Kiyohiro Akiyama, Futoshi Sakamoto, Goi Kasumi, Fujio Miki, Yoshio Tanaka, Toshihiro Tsunoda, Tatsuhiko |
description | Estrogen receptor (ER) status is an essential determinant of clinical and biological behavior of human breast cancers. While ER‐positive breast cancers respond well to adjuvant hormone therapy, ER‐negative tumors are generally resistant. To date, no attempts have succeeded in finding molecular markers for classifying ER‐negative breast cancers with respect to postoperative prognosis. To identify a set of prognostic markers for this type of cancer, we used a cDNA microarray consisting of 25,344 human genes to investigate expression profiles of ten primary breast cancers from patients who had died of breast cancer within 5 years after surgery (5y‐D) and 10 from patients who had survived disease‐free for more than 5 years (5y‐S). Sets of genes characterizing each group were identified by Mann‐Whitney and random‐permutation tests. We documented 71 genes with higher expression in the 5y‐D group than in the 5y‐S group, and 15 with higher expression in the 5y‐S group than in the 5y‐D group. Semi‐quantitative RT‐PCR experiments were carried out to confirm the results of the microarray analysis. We established a scoring system for predicting postoperative prognosis of ER‐negative breast cancers on the basis of aberrant gene expression. The list of genes reported here provides valuable information with regard to progression of breast cancer and is a source of possible target molecules for development of novel drugs to treat patients with ER‐negative breast cancers. |
doi_str_mv | 10.1111/j.1349-7006.2004.tb02206.x |
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While ER‐positive breast cancers respond well to adjuvant hormone therapy, ER‐negative tumors are generally resistant. To date, no attempts have succeeded in finding molecular markers for classifying ER‐negative breast cancers with respect to postoperative prognosis. To identify a set of prognostic markers for this type of cancer, we used a cDNA microarray consisting of 25,344 human genes to investigate expression profiles of ten primary breast cancers from patients who had died of breast cancer within 5 years after surgery (5y‐D) and 10 from patients who had survived disease‐free for more than 5 years (5y‐S). Sets of genes characterizing each group were identified by Mann‐Whitney and random‐permutation tests. We documented 71 genes with higher expression in the 5y‐D group than in the 5y‐S group, and 15 with higher expression in the 5y‐S group than in the 5y‐D group. Semi‐quantitative RT‐PCR experiments were carried out to confirm the results of the microarray analysis. We established a scoring system for predicting postoperative prognosis of ER‐negative breast cancers on the basis of aberrant gene expression. The list of genes reported here provides valuable information with regard to progression of breast cancer and is a source of possible target molecules for development of novel drugs to treat patients with ER‐negative breast cancers.</description><identifier>ISSN: 1347-9032</identifier><identifier>EISSN: 1349-7006</identifier><identifier>DOI: 10.1111/j.1349-7006.2004.tb02206.x</identifier><identifier>PMID: 15016320</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adult ; Aged ; Biological and medical sciences ; Biomarkers, Tumor - analysis ; Breast cancer ; Breast Neoplasms - genetics ; Breast Neoplasms - pathology ; Disease Progression ; DNA microarrays ; DNA Primers ; Drug development ; Estrogen receptors ; Female ; Gene expression ; Gene Expression Profiling ; Gene Expression Regulation, Neoplastic ; Gynecology. Andrology. Obstetrics ; Humans ; Mammary gland diseases ; Medical sciences ; Middle Aged ; Neoplasm Invasiveness ; Oligonucleotide Array Sequence Analysis ; Patients ; Postoperative Period ; Prognosis ; Receptors, Estrogen - metabolism ; Reverse Transcriptase Polymerase Chain Reaction ; RNA, Neoplasm - analysis ; Surgery ; Tumors</subject><ispartof>Cancer science, 2004-03, Vol.95 (3), p.218-225</ispartof><rights>2004 INIST-CNRS</rights><rights>Copyright John Wiley & Sons, Inc. Mar 2004</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6578-d8b8b0f2c5209d95b76108642c62cbfc46e7985c412c4e76c7ce748f5d2a7bbd3</citedby><cites>FETCH-LOGICAL-c6578-d8b8b0f2c5209d95b76108642c62cbfc46e7985c412c4e76c7ce748f5d2a7bbd3</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/PMC11160046/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11160046/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,1417,11562,27924,27925,45574,45575,46052,46476,53791,53793</link.rule.ids><linktorsrc>$$Uhttps://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1349-7006.2004.tb02206.x$$EView_record_in_Wiley-Blackwell$$FView_record_in_$$GWiley-Blackwell</linktorsrc><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15707738$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15016320$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nagahata, Takemitsu</creatorcontrib><creatorcontrib>Onda, Masamitsu</creatorcontrib><creatorcontrib>Emi, Mitsuru</creatorcontrib><creatorcontrib>Nagai, Hisaki</creatorcontrib><creatorcontrib>Tsumagari, Koji</creatorcontrib><creatorcontrib>Fujimoto, Takashi</creatorcontrib><creatorcontrib>Hirano, Akira</creatorcontrib><creatorcontrib>Sato, Takamichi</creatorcontrib><creatorcontrib>Nishikawa, Kiyohiro</creatorcontrib><creatorcontrib>Akiyama, Futoshi</creatorcontrib><creatorcontrib>Sakamoto, Goi</creatorcontrib><creatorcontrib>Kasumi, Fujio</creatorcontrib><creatorcontrib>Miki, Yoshio</creatorcontrib><creatorcontrib>Tanaka, Toshihiro</creatorcontrib><creatorcontrib>Tsunoda, Tatsuhiko</creatorcontrib><title>Expression profiling to predict postoperative prognosis for estrogen receptor‐negative breast cancers by analysis of 25,344 genes on a cDNA microarray</title><title>Cancer science</title><addtitle>Cancer Sci</addtitle><description>Estrogen receptor (ER) status is an essential determinant of clinical and biological behavior of human breast cancers. While ER‐positive breast cancers respond well to adjuvant hormone therapy, ER‐negative tumors are generally resistant. To date, no attempts have succeeded in finding molecular markers for classifying ER‐negative breast cancers with respect to postoperative prognosis. To identify a set of prognostic markers for this type of cancer, we used a cDNA microarray consisting of 25,344 human genes to investigate expression profiles of ten primary breast cancers from patients who had died of breast cancer within 5 years after surgery (5y‐D) and 10 from patients who had survived disease‐free for more than 5 years (5y‐S). Sets of genes characterizing each group were identified by Mann‐Whitney and random‐permutation tests. We documented 71 genes with higher expression in the 5y‐D group than in the 5y‐S group, and 15 with higher expression in the 5y‐S group than in the 5y‐D group. Semi‐quantitative RT‐PCR experiments were carried out to confirm the results of the microarray analysis. We established a scoring system for predicting postoperative prognosis of ER‐negative breast cancers on the basis of aberrant gene expression. The list of genes reported here provides valuable information with regard to progression of breast cancer and is a source of possible target molecules for development of novel drugs to treat patients with ER‐negative breast cancers.</description><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Biomarkers, Tumor - analysis</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - genetics</subject><subject>Breast Neoplasms - pathology</subject><subject>Disease Progression</subject><subject>DNA microarrays</subject><subject>DNA Primers</subject><subject>Drug development</subject><subject>Estrogen receptors</subject><subject>Female</subject><subject>Gene expression</subject><subject>Gene Expression Profiling</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Mammary gland diseases</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neoplasm Invasiveness</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>Patients</subject><subject>Postoperative Period</subject><subject>Prognosis</subject><subject>Receptors, Estrogen - metabolism</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Neoplasm - analysis</subject><subject>Surgery</subject><subject>Tumors</subject><issn>1347-9032</issn><issn>1349-7006</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</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><recordid>eNqVkc2O0zAUhSMEYoaBV0AWCFak-C92wgJUleFHGsECWFu2c1NcpXaw06HZ8QgseT6eBIdWw8AOb-wjf_f6-pyieEDwguT1dLMgjDelxFgsKMZ8MRpMaRb7G8Xp1dXN32dZNpjRk-JOShuMmeANv12ckAoTwSg-LX6c74cIKbng0RBD53rn12gMWUDr7IiGkMYwQNSju4QZWfuQXEJdiAjSmDV4FMHCMIb489t3D-sDaiLoNCKrvYWYkJmQ9rqf5trQIVo9YZyjXAxZe6SRffluibbOxqBj1NPd4lan-wT3jvtZ8enV-cfVm_Li_eu3q-VFaUUl67KtTW1wR21FcdM2lZGC4FpwagW1prNcgGzqynJCLQcprLQged1VLdXSmJadFS8OfYed2UJrwY9R92qIbqvjpIJ26u8b7z6rdbhUOQmRzRe5w-Njhxi-7LInauuShb7XHsIuKUkkx5XkGXz4D7gJu5hNSYqypuGMyIZk6tmByk6kFKG7moXg-VGiNmoOWc0hqzl_dcxf7XPx_eu_-VN6DDwDj46ATlb3XczxuHSNk1hKVmfu-YH76nqY_mMEtVp-oKRmvwBu0tEf</recordid><startdate>200403</startdate><enddate>200403</enddate><creator>Nagahata, Takemitsu</creator><creator>Onda, Masamitsu</creator><creator>Emi, Mitsuru</creator><creator>Nagai, Hisaki</creator><creator>Tsumagari, Koji</creator><creator>Fujimoto, Takashi</creator><creator>Hirano, Akira</creator><creator>Sato, Takamichi</creator><creator>Nishikawa, Kiyohiro</creator><creator>Akiyama, Futoshi</creator><creator>Sakamoto, Goi</creator><creator>Kasumi, Fujio</creator><creator>Miki, Yoshio</creator><creator>Tanaka, Toshihiro</creator><creator>Tsunoda, Tatsuhiko</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><general>John Wiley & Sons, Inc</general><scope>IQODW</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>8FE</scope><scope>8FH</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>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>200403</creationdate><title>Expression profiling to predict postoperative prognosis for estrogen receptor‐negative breast cancers by analysis of 25,344 genes on a cDNA microarray</title><author>Nagahata, Takemitsu ; Onda, Masamitsu ; Emi, Mitsuru ; Nagai, Hisaki ; Tsumagari, Koji ; Fujimoto, Takashi ; Hirano, Akira ; Sato, Takamichi ; Nishikawa, Kiyohiro ; Akiyama, Futoshi ; Sakamoto, Goi ; Kasumi, Fujio ; Miki, Yoshio ; Tanaka, Toshihiro ; Tsunoda, Tatsuhiko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6578-d8b8b0f2c5209d95b76108642c62cbfc46e7985c412c4e76c7ce748f5d2a7bbd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor - analysis</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - genetics</topic><topic>Breast Neoplasms - pathology</topic><topic>Disease Progression</topic><topic>DNA microarrays</topic><topic>DNA Primers</topic><topic>Drug development</topic><topic>Estrogen receptors</topic><topic>Female</topic><topic>Gene expression</topic><topic>Gene Expression Profiling</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Mammary gland diseases</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neoplasm Invasiveness</topic><topic>Oligonucleotide Array Sequence Analysis</topic><topic>Patients</topic><topic>Postoperative Period</topic><topic>Prognosis</topic><topic>Receptors, Estrogen - metabolism</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Neoplasm - analysis</topic><topic>Surgery</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nagahata, Takemitsu</creatorcontrib><creatorcontrib>Onda, Masamitsu</creatorcontrib><creatorcontrib>Emi, Mitsuru</creatorcontrib><creatorcontrib>Nagai, Hisaki</creatorcontrib><creatorcontrib>Tsumagari, Koji</creatorcontrib><creatorcontrib>Fujimoto, Takashi</creatorcontrib><creatorcontrib>Hirano, Akira</creatorcontrib><creatorcontrib>Sato, Takamichi</creatorcontrib><creatorcontrib>Nishikawa, Kiyohiro</creatorcontrib><creatorcontrib>Akiyama, Futoshi</creatorcontrib><creatorcontrib>Sakamoto, Goi</creatorcontrib><creatorcontrib>Kasumi, Fujio</creatorcontrib><creatorcontrib>Miki, Yoshio</creatorcontrib><creatorcontrib>Tanaka, Toshihiro</creatorcontrib><creatorcontrib>Tsunoda, Tatsuhiko</creatorcontrib><collection>Pascal-Francis</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 SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>Proquest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</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>PubMed Central (Full Participant titles)</collection><jtitle>Cancer science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Nagahata, Takemitsu</au><au>Onda, Masamitsu</au><au>Emi, Mitsuru</au><au>Nagai, Hisaki</au><au>Tsumagari, Koji</au><au>Fujimoto, Takashi</au><au>Hirano, Akira</au><au>Sato, Takamichi</au><au>Nishikawa, Kiyohiro</au><au>Akiyama, Futoshi</au><au>Sakamoto, Goi</au><au>Kasumi, Fujio</au><au>Miki, Yoshio</au><au>Tanaka, Toshihiro</au><au>Tsunoda, Tatsuhiko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression profiling to predict postoperative prognosis for estrogen receptor‐negative breast cancers by analysis of 25,344 genes on a cDNA microarray</atitle><jtitle>Cancer science</jtitle><addtitle>Cancer Sci</addtitle><date>2004-03</date><risdate>2004</risdate><volume>95</volume><issue>3</issue><spage>218</spage><epage>225</epage><pages>218-225</pages><issn>1347-9032</issn><eissn>1349-7006</eissn><abstract>Estrogen receptor (ER) status is an essential determinant of clinical and biological behavior of human breast cancers. While ER‐positive breast cancers respond well to adjuvant hormone therapy, ER‐negative tumors are generally resistant. To date, no attempts have succeeded in finding molecular markers for classifying ER‐negative breast cancers with respect to postoperative prognosis. To identify a set of prognostic markers for this type of cancer, we used a cDNA microarray consisting of 25,344 human genes to investigate expression profiles of ten primary breast cancers from patients who had died of breast cancer within 5 years after surgery (5y‐D) and 10 from patients who had survived disease‐free for more than 5 years (5y‐S). Sets of genes characterizing each group were identified by Mann‐Whitney and random‐permutation tests. We documented 71 genes with higher expression in the 5y‐D group than in the 5y‐S group, and 15 with higher expression in the 5y‐S group than in the 5y‐D group. Semi‐quantitative RT‐PCR experiments were carried out to confirm the results of the microarray analysis. We established a scoring system for predicting postoperative prognosis of ER‐negative breast cancers on the basis of aberrant gene expression. The list of genes reported here provides valuable information with regard to progression of breast cancer and is a source of possible target molecules for development of novel drugs to treat patients with ER‐negative breast cancers.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>15016320</pmid><doi>10.1111/j.1349-7006.2004.tb02206.x</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Biological and medical sciences Biomarkers, Tumor - analysis Breast cancer Breast Neoplasms - genetics Breast Neoplasms - pathology Disease Progression DNA microarrays DNA Primers Drug development Estrogen receptors Female Gene expression Gene Expression Profiling Gene Expression Regulation, Neoplastic Gynecology. Andrology. Obstetrics Humans Mammary gland diseases Medical sciences Middle Aged Neoplasm Invasiveness Oligonucleotide Array Sequence Analysis Patients Postoperative Period Prognosis Receptors, Estrogen - metabolism Reverse Transcriptase Polymerase Chain Reaction RNA, Neoplasm - analysis Surgery Tumors |
title | Expression profiling to predict postoperative prognosis for estrogen receptor‐negative breast cancers by analysis of 25,344 genes on a cDNA microarray |
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