Nuclear corepressor 1 expression predicts response to first-line endocrine therapy for breast cancer patients on relapse
Background Estrogen receptor alpha (ER α) is the most important endocrine therapy responsiveness predictor for women with breast cancer. The accuracy of the prediction of the response to endocrine therapy was thought to be affected by involving the estrogen receptor coregulatory proteins and cross-t...
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Veröffentlicht in: | Chinese medical journal 2009-08, Vol.122 (15), p.1764-1768 |
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creator | Zhang, Zhen-huan Yamashita, Hiroko Toyama, Tatsuya Yamamoto, Yutaka Kawasoe, Teru Ibusuki, Mutsuko Tomita, Saori Sugiura, Hiroshi Kobayashi, Shunzo Fujii, Yoshitaka Iwase, Hirotaka |
description | Background Estrogen receptor alpha (ER α) is the most important endocrine therapy responsiveness predictor for women with breast cancer. The accuracy of the prediction of the response to endocrine therapy was thought to be affected by involving the estrogen receptor coregulatory proteins and cross-talk between ER and other growth factor-signaling networks. Nuclear corepressor 1 (NCOR1) is one of the ER a transcription repressor. The objective of the study is to investigate the expression of NCOR1 at the protein level and pursue its predictive value for breast cancer endocrine therapy. Methods In the present study, the level of expression of NCOR1 protein has been assessed by immunohistochemistry in 104 cases of invasive carcinoma of the breast. Associations between NCOR1 protein expression and different clinicopathological factors and survival were sought. Results It was found that NCOR1 was expressed at significantly higher levels in responsive patients treated with endocrine therapy as first-line treatment on relapse. Responsive patients also had a significantly longer post-relapse survival and overall survival. No NCOR1 expression difference was found between patient by age, tumor size, lymph node status, different histological grade groups and human epidermal growth factor receptor 2 (HER2) status. Multivariate analysis showed that NCOR1 is an independent prognostic factor for over-all survival. Conclusions In breast cancer, NCOR1 protein expression level predicts response to endocrine therapy as first-line treatment for breast cancer patients on relapse and NCOR1 protein level assay may increase the accuracy in the endocrine treatment determination and, therefore, improving the patients survival. |
doi_str_mv | 10.3760/cma.j.issn.0366-6999.2009.15.009 |
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The accuracy of the prediction of the response to endocrine therapy was thought to be affected by involving the estrogen receptor coregulatory proteins and cross-talk between ER and other growth factor-signaling networks. Nuclear corepressor 1 (NCOR1) is one of the ER a transcription repressor. The objective of the study is to investigate the expression of NCOR1 at the protein level and pursue its predictive value for breast cancer endocrine therapy. Methods In the present study, the level of expression of NCOR1 protein has been assessed by immunohistochemistry in 104 cases of invasive carcinoma of the breast. Associations between NCOR1 protein expression and different clinicopathological factors and survival were sought. Results It was found that NCOR1 was expressed at significantly higher levels in responsive patients treated with endocrine therapy as first-line treatment on relapse. Responsive patients also had a significantly longer post-relapse survival and overall survival. No NCOR1 expression difference was found between patient by age, tumor size, lymph node status, different histological grade groups and human epidermal growth factor receptor 2 (HER2) status. Multivariate analysis showed that NCOR1 is an independent prognostic factor for over-all survival. Conclusions In breast cancer, NCOR1 protein expression level predicts response to endocrine therapy as first-line treatment for breast cancer patients on relapse and NCOR1 protein level assay may increase the accuracy in the endocrine treatment determination and, therefore, improving the patients survival.</description><identifier>ISSN: 0366-6999</identifier><identifier>EISSN: 2542-5641</identifier><identifier>DOI: 10.3760/cma.j.issn.0366-6999.2009.15.009</identifier><identifier>PMID: 19781322</identifier><language>eng</language><publisher>China: Department of Oncology and Immunology,Nagoya City University Graduate School of Medical Sciences,Kawasumi 1,Mizuho-ku,Nagoya 467-8601,Japan%Department of Oncology and Immunology,Nagoya City University Graduate School of Medical Sciences,Kawasumi 1,Mizuho-ku,Nagoya 467-8601,Japan%Department of Breast and Endocrine Surgery,Faculty of Medical and Pharmaceutical Sciences,Kumamoto University,Honjo 1-1-1Kumamoto 860-8556,Japan</publisher><subject>Antineoplastic Agents, Hormonal - therapeutic use ; Breast Neoplasms - drug therapy ; Breast Neoplasms - metabolism ; Estrogen Receptor alpha - metabolism ; Female ; Gene Expression Regulation ; Humans ; Immunohistochemistry ; Middle Aged ; Nuclear Receptor Co-Repressor 1 - metabolism ; Receptor, ErbB-2 - metabolism ; Receptors, Progesterone - metabolism ; Tamoxifen - therapeutic use ; 乳腺癌 ; 内分泌</subject><ispartof>Chinese medical journal, 2009-08, Vol.122 (15), p.1764-1768</ispartof><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/85656X/85656X.jpg</thumbnail><link.rule.ids>314,780,784,864,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19781322$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Zhen-huan</creatorcontrib><creatorcontrib>Yamashita, Hiroko</creatorcontrib><creatorcontrib>Toyama, Tatsuya</creatorcontrib><creatorcontrib>Yamamoto, Yutaka</creatorcontrib><creatorcontrib>Kawasoe, Teru</creatorcontrib><creatorcontrib>Ibusuki, Mutsuko</creatorcontrib><creatorcontrib>Tomita, Saori</creatorcontrib><creatorcontrib>Sugiura, Hiroshi</creatorcontrib><creatorcontrib>Kobayashi, Shunzo</creatorcontrib><creatorcontrib>Fujii, Yoshitaka</creatorcontrib><creatorcontrib>Iwase, Hirotaka</creatorcontrib><title>Nuclear corepressor 1 expression predicts response to first-line endocrine therapy for breast cancer patients on relapse</title><title>Chinese medical journal</title><addtitle>Chinese Medical Journal</addtitle><description>Background Estrogen receptor alpha (ER α) is the most important endocrine therapy responsiveness predictor for women with breast cancer. The accuracy of the prediction of the response to endocrine therapy was thought to be affected by involving the estrogen receptor coregulatory proteins and cross-talk between ER and other growth factor-signaling networks. Nuclear corepressor 1 (NCOR1) is one of the ER a transcription repressor. The objective of the study is to investigate the expression of NCOR1 at the protein level and pursue its predictive value for breast cancer endocrine therapy. Methods In the present study, the level of expression of NCOR1 protein has been assessed by immunohistochemistry in 104 cases of invasive carcinoma of the breast. Associations between NCOR1 protein expression and different clinicopathological factors and survival were sought. Results It was found that NCOR1 was expressed at significantly higher levels in responsive patients treated with endocrine therapy as first-line treatment on relapse. Responsive patients also had a significantly longer post-relapse survival and overall survival. No NCOR1 expression difference was found between patient by age, tumor size, lymph node status, different histological grade groups and human epidermal growth factor receptor 2 (HER2) status. Multivariate analysis showed that NCOR1 is an independent prognostic factor for over-all survival. Conclusions In breast cancer, NCOR1 protein expression level predicts response to endocrine therapy as first-line treatment for breast cancer patients on relapse and NCOR1 protein level assay may increase the accuracy in the endocrine treatment determination and, therefore, improving the patients survival.</description><subject>Antineoplastic Agents, Hormonal - therapeutic use</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - metabolism</subject><subject>Estrogen Receptor alpha - metabolism</subject><subject>Female</subject><subject>Gene Expression Regulation</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Middle Aged</subject><subject>Nuclear Receptor Co-Repressor 1 - metabolism</subject><subject>Receptor, ErbB-2 - metabolism</subject><subject>Receptors, Progesterone - metabolism</subject><subject>Tamoxifen - therapeutic use</subject><subject>乳腺癌</subject><subject>内分泌</subject><issn>0366-6999</issn><issn>2542-5641</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kE9v1DAQxS0EotvCV6isHqCXBP-LnRyrCtpKFVzgHDmz4663iZ3aiWj59Lhsy2Xe0-inN5pHyDlntTSafYHJ1vva5xxqJrWudNd1tWCsq3lTF3lDNqJRomq04m_J5j9zRI5z3jMmmsbo9-SId6blUogNefy-wog2UYgJ54Q5x0Q5xcd_3sdAi9l6WDItizmGjHSJ1PmUl2r0ASmGbYT07JYdJjs_UVcihoQ2LxRsAEx0tovHUDJKXsLRzhk_kHfOjhk_vugJ-fXt68_L6-r2x9XN5cVtBUK3S-UMtoDQtJbDViIHRKcMKFBSGMadNUogU65DkGywbafLYwrEAINBGJg8IZ8Oub9tcDbc9fu4plAu9n92MO2fy-NNGQX8fADnFB9WzEs_-Qw4jjZgXHNvpGJaMs0LefpCrsOE235OfrLpqX9ttQBnBwB2Mdw9-HJ1sHDv_Ii95II3nVHyL_wwjHw</recordid><startdate>20090805</startdate><enddate>20090805</enddate><creator>Zhang, Zhen-huan</creator><creator>Yamashita, Hiroko</creator><creator>Toyama, Tatsuya</creator><creator>Yamamoto, Yutaka</creator><creator>Kawasoe, Teru</creator><creator>Ibusuki, Mutsuko</creator><creator>Tomita, Saori</creator><creator>Sugiura, Hiroshi</creator><creator>Kobayashi, Shunzo</creator><creator>Fujii, Yoshitaka</creator><creator>Iwase, Hirotaka</creator><general>Department of Oncology and Immunology,Nagoya City University Graduate School of Medical Sciences,Kawasumi 1,Mizuho-ku,Nagoya 467-8601,Japan%Department of Oncology and Immunology,Nagoya City University Graduate School of Medical Sciences,Kawasumi 1,Mizuho-ku,Nagoya 467-8601,Japan%Department of Breast and Endocrine Surgery,Faculty of Medical and Pharmaceutical Sciences,Kumamoto University,Honjo 1-1-1Kumamoto 860-8556,Japan</general><general>Department of Breast and Endocrine Surgery,Faculty of Medical and Pharmaceutical Sciences,Kumamoto University,Honjo 1-1-1Kumamoto 860-8556,Japan</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W95</scope><scope>~WA</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope></search><sort><creationdate>20090805</creationdate><title>Nuclear corepressor 1 expression predicts response to first-line endocrine therapy for breast cancer patients on relapse</title><author>Zhang, Zhen-huan ; Yamashita, Hiroko ; Toyama, Tatsuya ; Yamamoto, Yutaka ; Kawasoe, Teru ; Ibusuki, Mutsuko ; Tomita, Saori ; Sugiura, Hiroshi ; Kobayashi, Shunzo ; Fujii, Yoshitaka ; Iwase, Hirotaka</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c268t-f7e8cec58a1cd3e1ceef47c4c432701fa742e04f9ec30ba8968134c2bcb7ecb03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Antineoplastic Agents, Hormonal - therapeutic use</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Breast Neoplasms - metabolism</topic><topic>Estrogen Receptor alpha - metabolism</topic><topic>Female</topic><topic>Gene Expression Regulation</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Middle Aged</topic><topic>Nuclear Receptor Co-Repressor 1 - metabolism</topic><topic>Receptor, ErbB-2 - metabolism</topic><topic>Receptors, Progesterone - metabolism</topic><topic>Tamoxifen - therapeutic use</topic><topic>乳腺癌</topic><topic>内分泌</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Zhen-huan</creatorcontrib><creatorcontrib>Yamashita, Hiroko</creatorcontrib><creatorcontrib>Toyama, Tatsuya</creatorcontrib><creatorcontrib>Yamamoto, Yutaka</creatorcontrib><creatorcontrib>Kawasoe, Teru</creatorcontrib><creatorcontrib>Ibusuki, Mutsuko</creatorcontrib><creatorcontrib>Tomita, Saori</creatorcontrib><creatorcontrib>Sugiura, Hiroshi</creatorcontrib><creatorcontrib>Kobayashi, Shunzo</creatorcontrib><creatorcontrib>Fujii, Yoshitaka</creatorcontrib><creatorcontrib>Iwase, Hirotaka</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-农业科学</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><jtitle>Chinese medical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Zhen-huan</au><au>Yamashita, Hiroko</au><au>Toyama, Tatsuya</au><au>Yamamoto, Yutaka</au><au>Kawasoe, Teru</au><au>Ibusuki, Mutsuko</au><au>Tomita, Saori</au><au>Sugiura, Hiroshi</au><au>Kobayashi, Shunzo</au><au>Fujii, Yoshitaka</au><au>Iwase, Hirotaka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nuclear corepressor 1 expression predicts response to first-line endocrine therapy for breast cancer patients on relapse</atitle><jtitle>Chinese medical journal</jtitle><addtitle>Chinese Medical Journal</addtitle><date>2009-08-05</date><risdate>2009</risdate><volume>122</volume><issue>15</issue><spage>1764</spage><epage>1768</epage><pages>1764-1768</pages><issn>0366-6999</issn><eissn>2542-5641</eissn><abstract>Background Estrogen receptor alpha (ER α) is the most important endocrine therapy responsiveness predictor for women with breast cancer. The accuracy of the prediction of the response to endocrine therapy was thought to be affected by involving the estrogen receptor coregulatory proteins and cross-talk between ER and other growth factor-signaling networks. Nuclear corepressor 1 (NCOR1) is one of the ER a transcription repressor. The objective of the study is to investigate the expression of NCOR1 at the protein level and pursue its predictive value for breast cancer endocrine therapy. Methods In the present study, the level of expression of NCOR1 protein has been assessed by immunohistochemistry in 104 cases of invasive carcinoma of the breast. Associations between NCOR1 protein expression and different clinicopathological factors and survival were sought. Results It was found that NCOR1 was expressed at significantly higher levels in responsive patients treated with endocrine therapy as first-line treatment on relapse. Responsive patients also had a significantly longer post-relapse survival and overall survival. No NCOR1 expression difference was found between patient by age, tumor size, lymph node status, different histological grade groups and human epidermal growth factor receptor 2 (HER2) status. Multivariate analysis showed that NCOR1 is an independent prognostic factor for over-all survival. Conclusions In breast cancer, NCOR1 protein expression level predicts response to endocrine therapy as first-line treatment for breast cancer patients on relapse and NCOR1 protein level assay may increase the accuracy in the endocrine treatment determination and, therefore, improving the patients survival.</abstract><cop>China</cop><pub>Department of Oncology and Immunology,Nagoya City University Graduate School of Medical Sciences,Kawasumi 1,Mizuho-ku,Nagoya 467-8601,Japan%Department of Oncology and Immunology,Nagoya City University Graduate School of Medical Sciences,Kawasumi 1,Mizuho-ku,Nagoya 467-8601,Japan%Department of Breast and Endocrine Surgery,Faculty of Medical and Pharmaceutical Sciences,Kumamoto University,Honjo 1-1-1Kumamoto 860-8556,Japan</pub><pmid>19781322</pmid><doi>10.3760/cma.j.issn.0366-6999.2009.15.009</doi><tpages>5</tpages></addata></record> |
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subjects | Antineoplastic Agents, Hormonal - therapeutic use Breast Neoplasms - drug therapy Breast Neoplasms - metabolism Estrogen Receptor alpha - metabolism Female Gene Expression Regulation Humans Immunohistochemistry Middle Aged Nuclear Receptor Co-Repressor 1 - metabolism Receptor, ErbB-2 - metabolism Receptors, Progesterone - metabolism Tamoxifen - therapeutic use 乳腺癌 内分泌 |
title | Nuclear corepressor 1 expression predicts response to first-line endocrine therapy for breast cancer patients on relapse |
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