Gene Expression Profiles of Primary Breast Carcinomas from Patients at High Risk for Local Recurrence after Breast-Conserving Therapy
Purpose: Several risk factors for local recurrence of breast cancer after breast-conserving therapy (BCT) have been identified. The identification of additional risk factors would be very useful in guiding optimal therapy and also in improving understanding of the mechanisms underlying local recurre...
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creator | KREIKE, Bas HALFWERK, Hans KRISTEL, Petra GLAS, Annuska PETERSE, Hans BARTEIINK, Harry VAN DE VIJVER, Marc J |
description | Purpose: Several risk factors for local recurrence of breast cancer after breast-conserving therapy (BCT) have been identified. The
identification of additional risk factors would be very useful in guiding optimal therapy and also in improving understanding
of the mechanisms underlying local recurrence. We used cDNA microarray analysis to identify gene expression profiles associated
with local recurrence.
Experimental Design: Using 18K cDNA microarrays, gene expression profiles were obtained from 50 patients who underwent BCT. Of these 50 patients,
19 developed a local recurrence; the remaining 31 patients were selected as controls as they were free of local recurrence
at least 11 years after treatment. For 9 of 19 patients, the local recurrence was also available for gene expression profiling.
Unsupervised and supervised methods of classification were used to separate patients in groups corresponding to disease outcome
and to study the overall gene expression pattern of primary tumors and their recurrences.
Results: Hierarchical clustering of patients did not show any grouping reflecting local recurrence status. Supervised analysis revealed
no significant set of genes that was able to distinguish recurring tumors from nonrecurring tumors. Paired-data analysis of
primary tumors and local recurrences showed a remarkable similarity in gene expression profile between primary tumors and
their recurrences.
Conclusions: No significant differences in gene expression between primary breast cancer tumors in patients with or without local recurrence
after BCT were identified. Furthermore, analyses of primary tumors and local recurrences show a preservation of the overall
gene expression pattern in the local recurrence, even after radiotherapy. |
doi_str_mv | 10.1158/1078-0432.CCR-06-0805 |
format | Article |
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identification of additional risk factors would be very useful in guiding optimal therapy and also in improving understanding
of the mechanisms underlying local recurrence. We used cDNA microarray analysis to identify gene expression profiles associated
with local recurrence.
Experimental Design: Using 18K cDNA microarrays, gene expression profiles were obtained from 50 patients who underwent BCT. Of these 50 patients,
19 developed a local recurrence; the remaining 31 patients were selected as controls as they were free of local recurrence
at least 11 years after treatment. For 9 of 19 patients, the local recurrence was also available for gene expression profiling.
Unsupervised and supervised methods of classification were used to separate patients in groups corresponding to disease outcome
and to study the overall gene expression pattern of primary tumors and their recurrences.
Results: Hierarchical clustering of patients did not show any grouping reflecting local recurrence status. Supervised analysis revealed
no significant set of genes that was able to distinguish recurring tumors from nonrecurring tumors. Paired-data analysis of
primary tumors and local recurrences showed a remarkable similarity in gene expression profile between primary tumors and
their recurrences.
Conclusions: No significant differences in gene expression between primary breast cancer tumors in patients with or without local recurrence
after BCT were identified. Furthermore, analyses of primary tumors and local recurrences show a preservation of the overall
gene expression pattern in the local recurrence, even after radiotherapy.</description><identifier>ISSN: 1078-0432</identifier><identifier>EISSN: 1557-3265</identifier><identifier>DOI: 10.1158/1078-0432.CCR-06-0805</identifier><identifier>PMID: 17020974</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Adult ; Antineoplastic agents ; Biological and medical sciences ; Biomarkers, Tumor - genetics ; Biomarkers, Tumor - metabolism ; breast cancer ; breast conserving therapy ; Breast Neoplasms - genetics ; Breast Neoplasms - metabolism ; Breast Neoplasms - surgery ; Carcinoma, Ductal, Breast - genetics ; Carcinoma, Ductal, Breast - metabolism ; Carcinoma, Ductal, Breast - surgery ; Carcinoma, Lobular - genetics ; Carcinoma, Lobular - metabolism ; Carcinoma, Lobular - surgery ; Female ; Gene Expression Profiling ; Gynecology. Andrology. Obstetrics ; Humans ; local recurrence ; Mammary gland diseases ; Mastectomy, Segmental ; Medical sciences ; microarray ; Middle Aged ; Neoplasm Recurrence, Local - diagnosis ; Neoplasm Recurrence, Local - genetics ; Neoplasm Recurrence, Local - metabolism ; Neoplasm Staging ; Oligonucleotide Array Sequence Analysis ; Pharmacology. Drug treatments ; Prognosis ; Prospective Studies ; Risk Factors ; Tumors</subject><ispartof>Clinical cancer research, 2006-10, Vol.12 (19), p.5705-5712</ispartof><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c449t-e6b472ae84e8a7cf25368a53eca3f9c1ed6be44a6c557893bf56155c6eb5bdda3</citedby><cites>FETCH-LOGICAL-c449t-e6b472ae84e8a7cf25368a53eca3f9c1ed6be44a6c557893bf56155c6eb5bdda3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3356,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18210037$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17020974$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>KREIKE, Bas</creatorcontrib><creatorcontrib>HALFWERK, Hans</creatorcontrib><creatorcontrib>KRISTEL, Petra</creatorcontrib><creatorcontrib>GLAS, Annuska</creatorcontrib><creatorcontrib>PETERSE, Hans</creatorcontrib><creatorcontrib>BARTEIINK, Harry</creatorcontrib><creatorcontrib>VAN DE VIJVER, Marc J</creatorcontrib><title>Gene Expression Profiles of Primary Breast Carcinomas from Patients at High Risk for Local Recurrence after Breast-Conserving Therapy</title><title>Clinical cancer research</title><addtitle>Clin Cancer Res</addtitle><description>Purpose: Several risk factors for local recurrence of breast cancer after breast-conserving therapy (BCT) have been identified. The
identification of additional risk factors would be very useful in guiding optimal therapy and also in improving understanding
of the mechanisms underlying local recurrence. We used cDNA microarray analysis to identify gene expression profiles associated
with local recurrence.
Experimental Design: Using 18K cDNA microarrays, gene expression profiles were obtained from 50 patients who underwent BCT. Of these 50 patients,
19 developed a local recurrence; the remaining 31 patients were selected as controls as they were free of local recurrence
at least 11 years after treatment. For 9 of 19 patients, the local recurrence was also available for gene expression profiling.
Unsupervised and supervised methods of classification were used to separate patients in groups corresponding to disease outcome
and to study the overall gene expression pattern of primary tumors and their recurrences.
Results: Hierarchical clustering of patients did not show any grouping reflecting local recurrence status. Supervised analysis revealed
no significant set of genes that was able to distinguish recurring tumors from nonrecurring tumors. Paired-data analysis of
primary tumors and local recurrences showed a remarkable similarity in gene expression profile between primary tumors and
their recurrences.
Conclusions: No significant differences in gene expression between primary breast cancer tumors in patients with or without local recurrence
after BCT were identified. Furthermore, analyses of primary tumors and local recurrences show a preservation of the overall
gene expression pattern in the local recurrence, even after radiotherapy.</description><subject>Adult</subject><subject>Antineoplastic agents</subject><subject>Biological and medical sciences</subject><subject>Biomarkers, Tumor - genetics</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>breast cancer</subject><subject>breast conserving therapy</subject><subject>Breast Neoplasms - genetics</subject><subject>Breast Neoplasms - metabolism</subject><subject>Breast Neoplasms - surgery</subject><subject>Carcinoma, Ductal, Breast - genetics</subject><subject>Carcinoma, Ductal, Breast - metabolism</subject><subject>Carcinoma, Ductal, Breast - surgery</subject><subject>Carcinoma, Lobular - genetics</subject><subject>Carcinoma, Lobular - metabolism</subject><subject>Carcinoma, Lobular - surgery</subject><subject>Female</subject><subject>Gene Expression Profiling</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>local recurrence</subject><subject>Mammary gland diseases</subject><subject>Mastectomy, Segmental</subject><subject>Medical sciences</subject><subject>microarray</subject><subject>Middle Aged</subject><subject>Neoplasm Recurrence, Local - diagnosis</subject><subject>Neoplasm Recurrence, Local - genetics</subject><subject>Neoplasm Recurrence, Local - metabolism</subject><subject>Neoplasm Staging</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>Pharmacology. Drug treatments</subject><subject>Prognosis</subject><subject>Prospective Studies</subject><subject>Risk Factors</subject><subject>Tumors</subject><issn>1078-0432</issn><issn>1557-3265</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkctu1DAUhi0EoqXwCCBvQOoixY4vcZY06gVpJKpRWVuO57hjSOLBJwP0AXhvPJqgLlmds_jORf9HyFvOLjhX5iNnjamYFPVF160rpitmmHpGTrlSTSVqrZ6X_h9zQl4hfmOMS87kS3LCG1aztpGn5M8NTECvfu8yIMY00bucQhwAaQqlj6PLj_Qyg8OZdi77OKXRIQ05jfTOzRGmGamb6W182NJ1xO80pExXybuBrsHvc4bJA3Vhhrzsqbo0IeSfcXqg91vIbvf4mrwIbkB4s9Qz8vX66r67rVZfbj53n1aVl7KdK9C9bGoHRoJxjQ-1Eto4JcA7EVrPYaN7kNJpX0IwreiD0iUPr6FX_WbjxBn5cNy7y-nHHnC2Y0QPw-AmSHu02rS1ZkL8F-RtK6SpZQHVEfQ5IWYIdncMzXJmD6LsQYI9SLBFlGXaHkSVuXfLgX0_wuZpajFTgPcL4LCEGbKbfMQnztScMdEU7vzIbYuBXzGD9YWEkjtC8bW1vC7fWtWUo38BNLur4Q</recordid><startdate>20061001</startdate><enddate>20061001</enddate><creator>KREIKE, Bas</creator><creator>HALFWERK, Hans</creator><creator>KRISTEL, Petra</creator><creator>GLAS, Annuska</creator><creator>PETERSE, Hans</creator><creator>BARTEIINK, Harry</creator><creator>VAN DE VIJVER, Marc J</creator><general>American Association for Cancer Research</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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20061001</creationdate><title>Gene Expression Profiles of Primary Breast Carcinomas from Patients at High Risk for Local Recurrence after Breast-Conserving Therapy</title><author>KREIKE, Bas ; HALFWERK, Hans ; KRISTEL, Petra ; GLAS, Annuska ; PETERSE, Hans ; BARTEIINK, Harry ; VAN DE VIJVER, Marc J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c449t-e6b472ae84e8a7cf25368a53eca3f9c1ed6be44a6c557893bf56155c6eb5bdda3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adult</topic><topic>Antineoplastic agents</topic><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor - genetics</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>breast cancer</topic><topic>breast conserving therapy</topic><topic>Breast Neoplasms - genetics</topic><topic>Breast Neoplasms - metabolism</topic><topic>Breast Neoplasms - surgery</topic><topic>Carcinoma, Ductal, Breast - genetics</topic><topic>Carcinoma, Ductal, Breast - metabolism</topic><topic>Carcinoma, Ductal, Breast - surgery</topic><topic>Carcinoma, Lobular - genetics</topic><topic>Carcinoma, Lobular - metabolism</topic><topic>Carcinoma, Lobular - surgery</topic><topic>Female</topic><topic>Gene Expression Profiling</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>local recurrence</topic><topic>Mammary gland diseases</topic><topic>Mastectomy, Segmental</topic><topic>Medical sciences</topic><topic>microarray</topic><topic>Middle Aged</topic><topic>Neoplasm Recurrence, Local - diagnosis</topic><topic>Neoplasm Recurrence, Local - genetics</topic><topic>Neoplasm Recurrence, Local - metabolism</topic><topic>Neoplasm Staging</topic><topic>Oligonucleotide Array Sequence Analysis</topic><topic>Pharmacology. Drug treatments</topic><topic>Prognosis</topic><topic>Prospective Studies</topic><topic>Risk Factors</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KREIKE, Bas</creatorcontrib><creatorcontrib>HALFWERK, Hans</creatorcontrib><creatorcontrib>KRISTEL, Petra</creatorcontrib><creatorcontrib>GLAS, Annuska</creatorcontrib><creatorcontrib>PETERSE, Hans</creatorcontrib><creatorcontrib>BARTEIINK, Harry</creatorcontrib><creatorcontrib>VAN DE VIJVER, Marc J</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>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical cancer research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KREIKE, Bas</au><au>HALFWERK, Hans</au><au>KRISTEL, Petra</au><au>GLAS, Annuska</au><au>PETERSE, Hans</au><au>BARTEIINK, Harry</au><au>VAN DE VIJVER, Marc J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gene Expression Profiles of Primary Breast Carcinomas from Patients at High Risk for Local Recurrence after Breast-Conserving Therapy</atitle><jtitle>Clinical cancer research</jtitle><addtitle>Clin Cancer Res</addtitle><date>2006-10-01</date><risdate>2006</risdate><volume>12</volume><issue>19</issue><spage>5705</spage><epage>5712</epage><pages>5705-5712</pages><issn>1078-0432</issn><eissn>1557-3265</eissn><abstract>Purpose: Several risk factors for local recurrence of breast cancer after breast-conserving therapy (BCT) have been identified. The
identification of additional risk factors would be very useful in guiding optimal therapy and also in improving understanding
of the mechanisms underlying local recurrence. We used cDNA microarray analysis to identify gene expression profiles associated
with local recurrence.
Experimental Design: Using 18K cDNA microarrays, gene expression profiles were obtained from 50 patients who underwent BCT. Of these 50 patients,
19 developed a local recurrence; the remaining 31 patients were selected as controls as they were free of local recurrence
at least 11 years after treatment. For 9 of 19 patients, the local recurrence was also available for gene expression profiling.
Unsupervised and supervised methods of classification were used to separate patients in groups corresponding to disease outcome
and to study the overall gene expression pattern of primary tumors and their recurrences.
Results: Hierarchical clustering of patients did not show any grouping reflecting local recurrence status. Supervised analysis revealed
no significant set of genes that was able to distinguish recurring tumors from nonrecurring tumors. Paired-data analysis of
primary tumors and local recurrences showed a remarkable similarity in gene expression profile between primary tumors and
their recurrences.
Conclusions: No significant differences in gene expression between primary breast cancer tumors in patients with or without local recurrence
after BCT were identified. Furthermore, analyses of primary tumors and local recurrences show a preservation of the overall
gene expression pattern in the local recurrence, even after radiotherapy.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>17020974</pmid><doi>10.1158/1078-0432.CCR-06-0805</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; American Association for Cancer Research; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Adult Antineoplastic agents Biological and medical sciences Biomarkers, Tumor - genetics Biomarkers, Tumor - metabolism breast cancer breast conserving therapy Breast Neoplasms - genetics Breast Neoplasms - metabolism Breast Neoplasms - surgery Carcinoma, Ductal, Breast - genetics Carcinoma, Ductal, Breast - metabolism Carcinoma, Ductal, Breast - surgery Carcinoma, Lobular - genetics Carcinoma, Lobular - metabolism Carcinoma, Lobular - surgery Female Gene Expression Profiling Gynecology. Andrology. Obstetrics Humans local recurrence Mammary gland diseases Mastectomy, Segmental Medical sciences microarray Middle Aged Neoplasm Recurrence, Local - diagnosis Neoplasm Recurrence, Local - genetics Neoplasm Recurrence, Local - metabolism Neoplasm Staging Oligonucleotide Array Sequence Analysis Pharmacology. Drug treatments Prognosis Prospective Studies Risk Factors Tumors |
title | Gene Expression Profiles of Primary Breast Carcinomas from Patients at High Risk for Local Recurrence after Breast-Conserving Therapy |
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