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PRAME expression and clinical outcome of breast cancer
The tumour antigen PReferentially expressed Antigen of MElanoma (PRAME) is expressed in a variety of malignancies, including breast cancer. We have analysed PRAME gene expression in relation to clinical outcome for 295 primary breast cancer patients. Kaplan–Meier survival curves show a correlation o...
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Published in: | British journal of cancer 2008-08, Vol.99 (3), p.398-403 |
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creator | Epping, M T Hart, A A M Glas, A M Krijgsman, O Bernards, R |
description | The tumour antigen PReferentially expressed Antigen of MElanoma (PRAME) is expressed in a variety of malignancies, including breast cancer. We have analysed
PRAME
gene expression in relation to clinical outcome for 295 primary breast cancer patients. Kaplan–Meier survival curves show a correlation of
PRAME
expression levels with increased rates of distant metastases and decreased overall patient survival. This correlation existed both for the entire patient group (
n
=295) and for the subgroup of patients (
n
=185) who did not receive adjuvant chemotherapy. Multivariable analysis indicated that
PRAME
is an independent marker of shortened metastasis-free interval in patients who did not receive adjuvant chemotherapy.
PRAME
expression was associated with tumour grade and negative oestrogen receptor status. We conclude that
PRAME
expression is a prognostic marker for clinical outcome of breast cancer, independent of traditional clinicopathological markers. |
doi_str_mv | 10.1038/sj.bjc.6604494 |
format | article |
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PRAME
gene expression in relation to clinical outcome for 295 primary breast cancer patients. Kaplan–Meier survival curves show a correlation of
PRAME
expression levels with increased rates of distant metastases and decreased overall patient survival. This correlation existed both for the entire patient group (
n
=295) and for the subgroup of patients (
n
=185) who did not receive adjuvant chemotherapy. Multivariable analysis indicated that
PRAME
is an independent marker of shortened metastasis-free interval in patients who did not receive adjuvant chemotherapy.
PRAME
expression was associated with tumour grade and negative oestrogen receptor status. We conclude that
PRAME
expression is a prognostic marker for clinical outcome of breast cancer, independent of traditional clinicopathological markers.</description><identifier>ISSN: 0007-0920</identifier><identifier>EISSN: 1532-1827</identifier><identifier>DOI: 10.1038/sj.bjc.6604494</identifier><identifier>PMID: 18648365</identifier><identifier>CODEN: BJCAAI</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Antigens, Neoplasm - genetics ; Biological and medical sciences ; Biomedical and Life Sciences ; Biomedicine ; Breast cancer ; Breast Neoplasms - genetics ; Cancer Research ; Clinical outcomes ; Clinical Study ; Drug Resistance ; Epidemiology ; Gene Expression Profiling ; Gynecology. Andrology. Obstetrics ; Humans ; Mammary gland diseases ; Medical sciences ; Molecular Medicine ; Multivariate Analysis ; Oligonucleotide Array Sequence Analysis ; Oncology ; Prognosis ; Proportional Hazards Models ; Survival Analysis ; Treatment Outcome ; Tumors</subject><ispartof>British journal of cancer, 2008-08, Vol.99 (3), p.398-403</ispartof><rights>The Author(s) 2008</rights><rights>2008 INIST-CNRS</rights><rights>Copyright Nature Publishing Group Aug 5, 2008</rights><rights>Copyright © 2008 Cancer Research UK 2008 Cancer Research UK</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c551t-3c346b03898cb628a73efa5adc845739fc9dcac51e07f3833e11e01deaa9ad063</citedby><cites>FETCH-LOGICAL-c551t-3c346b03898cb628a73efa5adc845739fc9dcac51e07f3833e11e01deaa9ad063</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/PMC2527791/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2527791/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20588983$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18648365$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Epping, M T</creatorcontrib><creatorcontrib>Hart, A A M</creatorcontrib><creatorcontrib>Glas, A M</creatorcontrib><creatorcontrib>Krijgsman, O</creatorcontrib><creatorcontrib>Bernards, R</creatorcontrib><title>PRAME expression and clinical outcome of breast cancer</title><title>British journal of cancer</title><addtitle>Br J Cancer</addtitle><addtitle>Br J Cancer</addtitle><description>The tumour antigen PReferentially expressed Antigen of MElanoma (PRAME) is expressed in a variety of malignancies, including breast cancer. We have analysed
PRAME
gene expression in relation to clinical outcome for 295 primary breast cancer patients. Kaplan–Meier survival curves show a correlation of
PRAME
expression levels with increased rates of distant metastases and decreased overall patient survival. This correlation existed both for the entire patient group (
n
=295) and for the subgroup of patients (
n
=185) who did not receive adjuvant chemotherapy. Multivariable analysis indicated that
PRAME
is an independent marker of shortened metastasis-free interval in patients who did not receive adjuvant chemotherapy.
PRAME
expression was associated with tumour grade and negative oestrogen receptor status. We conclude that
PRAME
expression is a prognostic marker for clinical outcome of breast cancer, independent of traditional clinicopathological markers.</description><subject>Antigens, Neoplasm - genetics</subject><subject>Biological and medical sciences</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - genetics</subject><subject>Cancer Research</subject><subject>Clinical outcomes</subject><subject>Clinical Study</subject><subject>Drug Resistance</subject><subject>Epidemiology</subject><subject>Gene Expression Profiling</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Mammary gland diseases</subject><subject>Medical sciences</subject><subject>Molecular Medicine</subject><subject>Multivariate Analysis</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>Oncology</subject><subject>Prognosis</subject><subject>Proportional Hazards Models</subject><subject>Survival Analysis</subject><subject>Treatment Outcome</subject><subject>Tumors</subject><issn>0007-0920</issn><issn>1532-1827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNp1kM1LwzAYh4Mobk6vHqUIHlvz0aTJRRhjfsBEET2HNE1nS9fMpBX9781Y2fTgKQnvk_f34wHgHMEEQcKvfZ3ktU4Yg2kq0gMwRpTgGHGcHYIxhDCLocBwBE68r8NTQJ4dgxHiLOWE0TFgzy_Tx3lkvtbOeF_ZNlJtEemmaiutmsj2nbYrE9kyyp1Rvou0arVxp-CoVI03Z8M5AW-389fZfbx4unuYTRexphR1MdEkZXnoKbjOGeYqI6ZUVBWapzQjotSi0EpTZGBWEk6IQeGKCqOUUAVkZAJutnvXfb4yhTZt51Qj165aKfctrark30lbvcul_ZSY4iwTKCy4HBY4-9Eb38na9q4NnSUmECLBGQlQsoW0s947U-4CEJQbzdLXMmiWg-bw4eJ3rT0-eA3A1QAoHzyWLlir_I7DkPLgZJN8veV8GLVL4_b1_on-AWpblmE</recordid><startdate>20080805</startdate><enddate>20080805</enddate><creator>Epping, M T</creator><creator>Hart, A A M</creator><creator>Glas, A M</creator><creator>Krijgsman, O</creator><creator>Bernards, R</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><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>3V.</scope><scope>7RV</scope><scope>7TO</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>5PM</scope></search><sort><creationdate>20080805</creationdate><title>PRAME expression and clinical outcome of breast cancer</title><author>Epping, M T ; Hart, A A M ; Glas, A M ; Krijgsman, O ; Bernards, R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c551t-3c346b03898cb628a73efa5adc845739fc9dcac51e07f3833e11e01deaa9ad063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Antigens, Neoplasm - genetics</topic><topic>Biological and medical sciences</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - genetics</topic><topic>Cancer Research</topic><topic>Clinical outcomes</topic><topic>Clinical Study</topic><topic>Drug Resistance</topic><topic>Epidemiology</topic><topic>Gene Expression Profiling</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Mammary gland diseases</topic><topic>Medical sciences</topic><topic>Molecular Medicine</topic><topic>Multivariate Analysis</topic><topic>Oligonucleotide Array Sequence Analysis</topic><topic>Oncology</topic><topic>Prognosis</topic><topic>Proportional Hazards Models</topic><topic>Survival Analysis</topic><topic>Treatment Outcome</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Epping, M T</creatorcontrib><creatorcontrib>Hart, A A M</creatorcontrib><creatorcontrib>Glas, A M</creatorcontrib><creatorcontrib>Krijgsman, O</creatorcontrib><creatorcontrib>Bernards, R</creatorcontrib><collection>Springer Nature OA Free Journals</collection><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 Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</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 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>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science 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>PubMed Central (Full Participant titles)</collection><jtitle>British journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Epping, M T</au><au>Hart, A A M</au><au>Glas, A M</au><au>Krijgsman, O</au><au>Bernards, R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>PRAME expression and clinical outcome of breast cancer</atitle><jtitle>British journal of cancer</jtitle><stitle>Br J Cancer</stitle><addtitle>Br J Cancer</addtitle><date>2008-08-05</date><risdate>2008</risdate><volume>99</volume><issue>3</issue><spage>398</spage><epage>403</epage><pages>398-403</pages><issn>0007-0920</issn><eissn>1532-1827</eissn><coden>BJCAAI</coden><abstract>The tumour antigen PReferentially expressed Antigen of MElanoma (PRAME) is expressed in a variety of malignancies, including breast cancer. We have analysed
PRAME
gene expression in relation to clinical outcome for 295 primary breast cancer patients. Kaplan–Meier survival curves show a correlation of
PRAME
expression levels with increased rates of distant metastases and decreased overall patient survival. This correlation existed both for the entire patient group (
n
=295) and for the subgroup of patients (
n
=185) who did not receive adjuvant chemotherapy. Multivariable analysis indicated that
PRAME
is an independent marker of shortened metastasis-free interval in patients who did not receive adjuvant chemotherapy.
PRAME
expression was associated with tumour grade and negative oestrogen receptor status. We conclude that
PRAME
expression is a prognostic marker for clinical outcome of breast cancer, independent of traditional clinicopathological markers.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>18648365</pmid><doi>10.1038/sj.bjc.6604494</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antigens, Neoplasm - genetics Biological and medical sciences Biomedical and Life Sciences Biomedicine Breast cancer Breast Neoplasms - genetics Cancer Research Clinical outcomes Clinical Study Drug Resistance Epidemiology Gene Expression Profiling Gynecology. Andrology. Obstetrics Humans Mammary gland diseases Medical sciences Molecular Medicine Multivariate Analysis Oligonucleotide Array Sequence Analysis Oncology Prognosis Proportional Hazards Models Survival Analysis Treatment Outcome Tumors |
title | PRAME expression and clinical outcome of breast cancer |
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