Different prognostic significance of CD24 and CD44 expression in breast cancer according to hormone receptor status

Abstract Objective CD44+ CD24−/low -expressing tumor cells have been studied as tumorigenic stem cells in vitro study. This study was designed to determine the clinical implication of the CD44 and CD24 expression in breast cancer. Methods Tissue microarray blocks containing 643 consecutive cases of...

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Veröffentlicht in:Breast (Edinburgh) 2011-02, Vol.20 (1), p.78-85
Hauptverfasser: Kim, Hee Jeong, Kim, Mi-Jung, Ahn, Sei Hyun, Son, Byung Ho, Kim, Sung Bae, Ahn, Jin Hee, Noh, Woo Chul, Gong, Gyungyub
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container_end_page 85
container_issue 1
container_start_page 78
container_title Breast (Edinburgh)
container_volume 20
creator Kim, Hee Jeong
Kim, Mi-Jung
Ahn, Sei Hyun
Son, Byung Ho
Kim, Sung Bae
Ahn, Jin Hee
Noh, Woo Chul
Gong, Gyungyub
description Abstract Objective CD44+ CD24−/low -expressing tumor cells have been studied as tumorigenic stem cells in vitro study. This study was designed to determine the clinical implication of the CD44 and CD24 expression in breast cancer. Methods Tissue microarray blocks containing 643 consecutive cases of invasive breast carcinomas from 1993 to 1998 were immunostained for CD44 and CD24. The median follow-up period was 127 months. Results CD44− CD24+ phenotype was associated with frequent hormone receptor positivity and Her2/neu positivity ( P  = 0.000; Both). The CD44+ CD24− phenotype was inversely associated with lymph node metastasis ( P  = 0.002), and it showed positive associations with prolonged disease-free survival (DFS; P  = 0.003) and overall survival (OS; P  = 0.002). 10-year DFS and OS were 68.9% and 74.6% for CD24 negative group, 55.6% and 60.9% for CD24 positive group ( P  = 0.001; Both). 10-year DFS and OS were 62.2% and 68.1% for CD44 negative group, 73% and 77.7% for CD44 positive group ( P  = 0.012, P  = 0.013, respectively). In a multivariate analysis, CD24 expression was negatively related to OS only in the receptor positive group (Hazard ratio = 2.03; P  = 0.003; 95% CI: 1.27–3.24) and CD44 expression was positively related to OS only in the hormone receptor negative group (hazard ratio = 0.58; P  = 0.022; 95% CI: 0.36–0.92). Conclusions The CD44+ CD24− group is considered a favorable prognostic subgroup in breast cancer. CD24 expression was a poor prognosis marker in hormone receptor positive breast cancer, and CD44 expression was a good prognostic marker in the receptor negative group.
doi_str_mv 10.1016/j.breast.2010.08.001
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This study was designed to determine the clinical implication of the CD44 and CD24 expression in breast cancer. Methods Tissue microarray blocks containing 643 consecutive cases of invasive breast carcinomas from 1993 to 1998 were immunostained for CD44 and CD24. The median follow-up period was 127 months. Results CD44− CD24+ phenotype was associated with frequent hormone receptor positivity and Her2/neu positivity ( P  = 0.000; Both). The CD44+ CD24− phenotype was inversely associated with lymph node metastasis ( P  = 0.002), and it showed positive associations with prolonged disease-free survival (DFS; P  = 0.003) and overall survival (OS; P  = 0.002). 10-year DFS and OS were 68.9% and 74.6% for CD24 negative group, 55.6% and 60.9% for CD24 positive group ( P  = 0.001; Both). 10-year DFS and OS were 62.2% and 68.1% for CD44 negative group, 73% and 77.7% for CD44 positive group ( P  = 0.012, P  = 0.013, respectively). In a multivariate analysis, CD24 expression was negatively related to OS only in the receptor positive group (Hazard ratio = 2.03; P  = 0.003; 95% CI: 1.27–3.24) and CD44 expression was positively related to OS only in the hormone receptor negative group (hazard ratio = 0.58; P  = 0.022; 95% CI: 0.36–0.92). Conclusions The CD44+ CD24− group is considered a favorable prognostic subgroup in breast cancer. CD24 expression was a poor prognosis marker in hormone receptor positive breast cancer, and CD44 expression was a good prognostic marker in the receptor negative group.</description><identifier>ISSN: 0960-9776</identifier><identifier>EISSN: 1532-3080</identifier><identifier>DOI: 10.1016/j.breast.2010.08.001</identifier><identifier>PMID: 20810282</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Adult ; Breast cancer ; Breast Neoplasms - chemistry ; Breast Neoplasms - pathology ; Carcinoma - chemically induced ; Carcinoma - pathology ; CD24 ; CD24 Antigen - analysis ; CD44 ; Disease-Free Survival ; Female ; Hematology, Oncology and Palliative Medicine ; Hormone receptor status ; Humans ; Hyaluronan Receptors - analysis ; Middle Aged ; Multivariate Analysis ; Prognosis ; Proportional Hazards Models ; Receptor, ErbB-2 - analysis ; Receptors, Estrogen - analysis ; Receptors, Progesterone - analysis</subject><ispartof>Breast (Edinburgh), 2011-02, Vol.20 (1), p.78-85</ispartof><rights>Elsevier Ltd</rights><rights>2010 Elsevier Ltd</rights><rights>Copyright © 2010 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c528t-5fa63de1b974c8816fd1ea193068f2c8adb90a417ba384b6e7c72a1df7b1c18e3</citedby><cites>FETCH-LOGICAL-c528t-5fa63de1b974c8816fd1ea193068f2c8adb90a417ba384b6e7c72a1df7b1c18e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.breast.2010.08.001$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,45974</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20810282$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Hee Jeong</creatorcontrib><creatorcontrib>Kim, Mi-Jung</creatorcontrib><creatorcontrib>Ahn, Sei Hyun</creatorcontrib><creatorcontrib>Son, Byung Ho</creatorcontrib><creatorcontrib>Kim, Sung Bae</creatorcontrib><creatorcontrib>Ahn, Jin Hee</creatorcontrib><creatorcontrib>Noh, Woo Chul</creatorcontrib><creatorcontrib>Gong, Gyungyub</creatorcontrib><title>Different prognostic significance of CD24 and CD44 expression in breast cancer according to hormone receptor status</title><title>Breast (Edinburgh)</title><addtitle>Breast</addtitle><description>Abstract Objective CD44+ CD24−/low -expressing tumor cells have been studied as tumorigenic stem cells in vitro study. This study was designed to determine the clinical implication of the CD44 and CD24 expression in breast cancer. Methods Tissue microarray blocks containing 643 consecutive cases of invasive breast carcinomas from 1993 to 1998 were immunostained for CD44 and CD24. The median follow-up period was 127 months. Results CD44− CD24+ phenotype was associated with frequent hormone receptor positivity and Her2/neu positivity ( P  = 0.000; Both). The CD44+ CD24− phenotype was inversely associated with lymph node metastasis ( P  = 0.002), and it showed positive associations with prolonged disease-free survival (DFS; P  = 0.003) and overall survival (OS; P  = 0.002). 10-year DFS and OS were 68.9% and 74.6% for CD24 negative group, 55.6% and 60.9% for CD24 positive group ( P  = 0.001; Both). 10-year DFS and OS were 62.2% and 68.1% for CD44 negative group, 73% and 77.7% for CD44 positive group ( P  = 0.012, P  = 0.013, respectively). In a multivariate analysis, CD24 expression was negatively related to OS only in the receptor positive group (Hazard ratio = 2.03; P  = 0.003; 95% CI: 1.27–3.24) and CD44 expression was positively related to OS only in the hormone receptor negative group (hazard ratio = 0.58; P  = 0.022; 95% CI: 0.36–0.92). Conclusions The CD44+ CD24− group is considered a favorable prognostic subgroup in breast cancer. CD24 expression was a poor prognosis marker in hormone receptor positive breast cancer, and CD44 expression was a good prognostic marker in the receptor negative group.</description><subject>Adult</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - chemistry</subject><subject>Breast Neoplasms - pathology</subject><subject>Carcinoma - chemically induced</subject><subject>Carcinoma - pathology</subject><subject>CD24</subject><subject>CD24 Antigen - analysis</subject><subject>CD44</subject><subject>Disease-Free Survival</subject><subject>Female</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Hormone receptor status</subject><subject>Humans</subject><subject>Hyaluronan Receptors - analysis</subject><subject>Middle Aged</subject><subject>Multivariate Analysis</subject><subject>Prognosis</subject><subject>Proportional Hazards Models</subject><subject>Receptor, ErbB-2 - analysis</subject><subject>Receptors, Estrogen - analysis</subject><subject>Receptors, Progesterone - analysis</subject><issn>0960-9776</issn><issn>1532-3080</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUGPFCEQhYnRuLOr_8AYbp56LOhuoC8mZlZXk008qGdC08XI2AMj0Bv338vYqwcvnopUXlXxvkfICwZbBky8PmzHhCaXLYfaArUFYI_IhvUtb1pQ8JhsYBDQDFKKC3KZ8wEAhlaop-SCg2LAFd-QfO2dw4Sh0FOK-xBz8ZZmvw_eeWuCRRod3V3zjpow1UfXUfx5Spizj4H6QNdf0N_aRI21MU0-7GmJ9FtMxxiQJrR4KjHRXExZ8jPyxJk54_OHekW-vn_3Zfehuf1083H39raxPVel6Z0R7YRsHGRnlWLCTQwNG1oQynGrzDQOYDomR9OqbhQoreSGTU6OzDKF7RV5te6tzn4smIs--mxxnk3AuGSteuhFhSersluVNsWcEzp9Sv5o0r1moM-09UGvPvWZtgalK-069vLhwDIecfo79AdvFbxZBVht3nlMOluPFdTkK5Oip-j_d-HfBXb2oQYzf8d7zIe4pFARaqYz16A_nxM_B85q1kwOsv0Fzmiodg</recordid><startdate>20110201</startdate><enddate>20110201</enddate><creator>Kim, Hee Jeong</creator><creator>Kim, Mi-Jung</creator><creator>Ahn, Sei Hyun</creator><creator>Son, Byung Ho</creator><creator>Kim, Sung Bae</creator><creator>Ahn, Jin Hee</creator><creator>Noh, Woo Chul</creator><creator>Gong, Gyungyub</creator><general>Elsevier Ltd</general><scope>6I.</scope><scope>AAFTH</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>7X8</scope></search><sort><creationdate>20110201</creationdate><title>Different prognostic significance of CD24 and CD44 expression in breast cancer according to hormone receptor status</title><author>Kim, Hee Jeong ; Kim, Mi-Jung ; Ahn, Sei Hyun ; Son, Byung Ho ; Kim, Sung Bae ; Ahn, Jin Hee ; Noh, Woo Chul ; Gong, Gyungyub</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c528t-5fa63de1b974c8816fd1ea193068f2c8adb90a417ba384b6e7c72a1df7b1c18e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adult</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - chemistry</topic><topic>Breast Neoplasms - pathology</topic><topic>Carcinoma - chemically induced</topic><topic>Carcinoma - pathology</topic><topic>CD24</topic><topic>CD24 Antigen - analysis</topic><topic>CD44</topic><topic>Disease-Free Survival</topic><topic>Female</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Hormone receptor status</topic><topic>Humans</topic><topic>Hyaluronan Receptors - analysis</topic><topic>Middle Aged</topic><topic>Multivariate Analysis</topic><topic>Prognosis</topic><topic>Proportional Hazards Models</topic><topic>Receptor, ErbB-2 - analysis</topic><topic>Receptors, Estrogen - analysis</topic><topic>Receptors, Progesterone - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Hee Jeong</creatorcontrib><creatorcontrib>Kim, Mi-Jung</creatorcontrib><creatorcontrib>Ahn, Sei Hyun</creatorcontrib><creatorcontrib>Son, Byung Ho</creatorcontrib><creatorcontrib>Kim, Sung Bae</creatorcontrib><creatorcontrib>Ahn, Jin Hee</creatorcontrib><creatorcontrib>Noh, Woo Chul</creatorcontrib><creatorcontrib>Gong, Gyungyub</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Breast (Edinburgh)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Hee Jeong</au><au>Kim, Mi-Jung</au><au>Ahn, Sei Hyun</au><au>Son, Byung Ho</au><au>Kim, Sung Bae</au><au>Ahn, Jin Hee</au><au>Noh, Woo Chul</au><au>Gong, Gyungyub</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Different prognostic significance of CD24 and CD44 expression in breast cancer according to hormone receptor status</atitle><jtitle>Breast (Edinburgh)</jtitle><addtitle>Breast</addtitle><date>2011-02-01</date><risdate>2011</risdate><volume>20</volume><issue>1</issue><spage>78</spage><epage>85</epage><pages>78-85</pages><issn>0960-9776</issn><eissn>1532-3080</eissn><abstract>Abstract Objective CD44+ CD24−/low -expressing tumor cells have been studied as tumorigenic stem cells in vitro study. This study was designed to determine the clinical implication of the CD44 and CD24 expression in breast cancer. Methods Tissue microarray blocks containing 643 consecutive cases of invasive breast carcinomas from 1993 to 1998 were immunostained for CD44 and CD24. The median follow-up period was 127 months. Results CD44− CD24+ phenotype was associated with frequent hormone receptor positivity and Her2/neu positivity ( P  = 0.000; Both). The CD44+ CD24− phenotype was inversely associated with lymph node metastasis ( P  = 0.002), and it showed positive associations with prolonged disease-free survival (DFS; P  = 0.003) and overall survival (OS; P  = 0.002). 10-year DFS and OS were 68.9% and 74.6% for CD24 negative group, 55.6% and 60.9% for CD24 positive group ( P  = 0.001; Both). 10-year DFS and OS were 62.2% and 68.1% for CD44 negative group, 73% and 77.7% for CD44 positive group ( P  = 0.012, P  = 0.013, respectively). In a multivariate analysis, CD24 expression was negatively related to OS only in the receptor positive group (Hazard ratio = 2.03; P  = 0.003; 95% CI: 1.27–3.24) and CD44 expression was positively related to OS only in the hormone receptor negative group (hazard ratio = 0.58; P  = 0.022; 95% CI: 0.36–0.92). Conclusions The CD44+ CD24− group is considered a favorable prognostic subgroup in breast cancer. CD24 expression was a poor prognosis marker in hormone receptor positive breast cancer, and CD44 expression was a good prognostic marker in the receptor negative group.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>20810282</pmid><doi>10.1016/j.breast.2010.08.001</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Breast cancer
Breast Neoplasms - chemistry
Breast Neoplasms - pathology
Carcinoma - chemically induced
Carcinoma - pathology
CD24
CD24 Antigen - analysis
CD44
Disease-Free Survival
Female
Hematology, Oncology and Palliative Medicine
Hormone receptor status
Humans
Hyaluronan Receptors - analysis
Middle Aged
Multivariate Analysis
Prognosis
Proportional Hazards Models
Receptor, ErbB-2 - analysis
Receptors, Estrogen - analysis
Receptors, Progesterone - analysis
title Different prognostic significance of CD24 and CD44 expression in breast cancer according to hormone receptor status
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