Early growth response 1 and fatty acid synthase expression is altered in tumor adjacent prostate tissue and indicates field cancerization
BACKGROUND Field cancerization denotes the occurrence of molecular alterations in histologically normal tissues adjacent to tumors. In prostate cancer, identification of field cancerization has several potential clinical applications. However, prostate field cancerization remains ill defined. Our pr...
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Veröffentlicht in: | The Prostate 2012-08, Vol.72 (11), p.1159-1170 |
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creator | Jones, Anna C. Trujillo, Kristina A. Phillips, Genevieve K. Fleet, Trisha M. Murton, Jaclyn K. Severns, Virginia Shah, Satyan K. Davis, Michael S. Smith, Anthony Y. Griffith, Jeffrey K. Fischer, Edgar G. Bisoffi, Marco |
description | BACKGROUND
Field cancerization denotes the occurrence of molecular alterations in histologically normal tissues adjacent to tumors. In prostate cancer, identification of field cancerization has several potential clinical applications. However, prostate field cancerization remains ill defined. Our previous work has shown up‐regulated mRNA of the transcription factor early growth response 1 (EGR‐1) and the lipogenic enzyme fatty acid synthase (FAS) in tissues adjacent to prostate cancer.
METHODS
Immunofluorescence data were analyzed quantitatively by spectral imaging and linear unmixing to determine the protein expression levels of EGR‐1 and FAS in human cancerous, histologically normal adjacent, and disease‐free prostate tissues.
RESULTS
EGR‐1 expression was elevated in both structurally intact tumor adjacent (1.6× on average) and in tumor (3.0× on average) tissues compared to disease‐free tissues. In addition, the ratio of cytoplasmic versus nuclear EGR‐1 expression was elevated in both tumor adjacent and tumor tissues. Similarly, FAS expression was elevated in both tumor adjacent (2.7× on average) and in tumor (2.5× on average) compared to disease‐free tissues.
CONCLUSIONS
EGR‐1 and FAS expression is similarly deregulated in tumor and structurally intact adjacent prostate tissues and defines field cancerization. In cases with high suspicion of prostate cancer but negative biopsy, identification of field cancerization could help clinicians target areas for repeat biopsy. Field cancerization at surgical margins on prostatectomy specimen should also be looked at as a predictor of cancer recurrence. EGR‐1 and FAS could also serve as molecular targets for chemoprevention. Prostate 72:1159–1170, 2012. © 2011 Wiley Periodicals, Inc. |
doi_str_mv | 10.1002/pros.22465 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1022377269</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1022377269</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4035-f2aa974be6820ec6f828063d3f99eaacc1180ee3887383a3c1d5951c198abd5e3</originalsourceid><addsrcrecordid>eNp9kE1v1DAQhi0Eokvhwg9APiKkFH8ksXNEbXdBVC3iQ3CzZu0Jdck6i-2oDf-Af4232_bIaaSZZx7NvIS85OyIMybebuOYjoSo2-YRWXDWqYqxunlMFkwoVtVcqgPyLKUrxgrOxFNyIAQXqtPtgvw9hTjM9Gccr_MljZi2Y0hIOYXgaA85zxSsdzTNIV9CmeDNtlDJj4H6RGHIGNFRH2ieNmOk4K7AYsh0d1SGjDT7lCa89fngvC29RHuPg6MWgsXo_0AuuufkSQ9Dwhd39ZB8W55-PX5fnV2sPhy_O6tszWRT9QKgU_UaWy0Y2rbXQrNWOtl3HQJYy7lmiFJrJbUEablruoZb3mlYuwblIXm995YLf0-Ystn4ZHEYIOA4JcOZEFIp0XYFfbNHbXkmRezNNvoNxLlAZhe92X1pbqMv8Ks777TeoHtA77MuAN8D137A-T8q8-nzxZd7abXf8SnjzcMOxF-mVVI15vv5ynzkJ8vlef3DrOQ_XbOg7Q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1022377269</pqid></control><display><type>article</type><title>Early growth response 1 and fatty acid synthase expression is altered in tumor adjacent prostate tissue and indicates field cancerization</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Jones, Anna C. ; Trujillo, Kristina A. ; Phillips, Genevieve K. ; Fleet, Trisha M. ; Murton, Jaclyn K. ; Severns, Virginia ; Shah, Satyan K. ; Davis, Michael S. ; Smith, Anthony Y. ; Griffith, Jeffrey K. ; Fischer, Edgar G. ; Bisoffi, Marco</creator><creatorcontrib>Jones, Anna C. ; Trujillo, Kristina A. ; Phillips, Genevieve K. ; Fleet, Trisha M. ; Murton, Jaclyn K. ; Severns, Virginia ; Shah, Satyan K. ; Davis, Michael S. ; Smith, Anthony Y. ; Griffith, Jeffrey K. ; Fischer, Edgar G. ; Bisoffi, Marco</creatorcontrib><description>BACKGROUND
Field cancerization denotes the occurrence of molecular alterations in histologically normal tissues adjacent to tumors. In prostate cancer, identification of field cancerization has several potential clinical applications. However, prostate field cancerization remains ill defined. Our previous work has shown up‐regulated mRNA of the transcription factor early growth response 1 (EGR‐1) and the lipogenic enzyme fatty acid synthase (FAS) in tissues adjacent to prostate cancer.
METHODS
Immunofluorescence data were analyzed quantitatively by spectral imaging and linear unmixing to determine the protein expression levels of EGR‐1 and FAS in human cancerous, histologically normal adjacent, and disease‐free prostate tissues.
RESULTS
EGR‐1 expression was elevated in both structurally intact tumor adjacent (1.6× on average) and in tumor (3.0× on average) tissues compared to disease‐free tissues. In addition, the ratio of cytoplasmic versus nuclear EGR‐1 expression was elevated in both tumor adjacent and tumor tissues. Similarly, FAS expression was elevated in both tumor adjacent (2.7× on average) and in tumor (2.5× on average) compared to disease‐free tissues.
CONCLUSIONS
EGR‐1 and FAS expression is similarly deregulated in tumor and structurally intact adjacent prostate tissues and defines field cancerization. In cases with high suspicion of prostate cancer but negative biopsy, identification of field cancerization could help clinicians target areas for repeat biopsy. Field cancerization at surgical margins on prostatectomy specimen should also be looked at as a predictor of cancer recurrence. EGR‐1 and FAS could also serve as molecular targets for chemoprevention. Prostate 72:1159–1170, 2012. © 2011 Wiley Periodicals, Inc.</description><identifier>ISSN: 0270-4137</identifier><identifier>EISSN: 1097-0045</identifier><identifier>DOI: 10.1002/pros.22465</identifier><identifier>PMID: 22127986</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adenocarcinoma - genetics ; Adenocarcinoma - metabolism ; Adenocarcinoma - pathology ; Adult ; Aged ; Cells, Cultured ; early growth response 1 ; Early Growth Response Protein 1 - biosynthesis ; Early Growth Response Protein 1 - genetics ; fatty acid synthase ; Fatty Acid Synthases - biosynthesis ; Fatty Acid Synthases - genetics ; field cancerization ; Humans ; Immunohistochemistry ; Male ; Middle Aged ; Prostate - metabolism ; Prostate - pathology ; prostate cancer ; Prostatic Neoplasms - genetics ; Prostatic Neoplasms - metabolism ; Prostatic Neoplasms - pathology ; tumor adjacent ; Tumor Cells, Cultured</subject><ispartof>The Prostate, 2012-08, Vol.72 (11), p.1159-1170</ispartof><rights>Copyright © 2011 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4035-f2aa974be6820ec6f828063d3f99eaacc1180ee3887383a3c1d5951c198abd5e3</citedby><cites>FETCH-LOGICAL-c4035-f2aa974be6820ec6f828063d3f99eaacc1180ee3887383a3c1d5951c198abd5e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fpros.22465$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpros.22465$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22127986$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jones, Anna C.</creatorcontrib><creatorcontrib>Trujillo, Kristina A.</creatorcontrib><creatorcontrib>Phillips, Genevieve K.</creatorcontrib><creatorcontrib>Fleet, Trisha M.</creatorcontrib><creatorcontrib>Murton, Jaclyn K.</creatorcontrib><creatorcontrib>Severns, Virginia</creatorcontrib><creatorcontrib>Shah, Satyan K.</creatorcontrib><creatorcontrib>Davis, Michael S.</creatorcontrib><creatorcontrib>Smith, Anthony Y.</creatorcontrib><creatorcontrib>Griffith, Jeffrey K.</creatorcontrib><creatorcontrib>Fischer, Edgar G.</creatorcontrib><creatorcontrib>Bisoffi, Marco</creatorcontrib><title>Early growth response 1 and fatty acid synthase expression is altered in tumor adjacent prostate tissue and indicates field cancerization</title><title>The Prostate</title><addtitle>Prostate</addtitle><description>BACKGROUND
Field cancerization denotes the occurrence of molecular alterations in histologically normal tissues adjacent to tumors. In prostate cancer, identification of field cancerization has several potential clinical applications. However, prostate field cancerization remains ill defined. Our previous work has shown up‐regulated mRNA of the transcription factor early growth response 1 (EGR‐1) and the lipogenic enzyme fatty acid synthase (FAS) in tissues adjacent to prostate cancer.
METHODS
Immunofluorescence data were analyzed quantitatively by spectral imaging and linear unmixing to determine the protein expression levels of EGR‐1 and FAS in human cancerous, histologically normal adjacent, and disease‐free prostate tissues.
RESULTS
EGR‐1 expression was elevated in both structurally intact tumor adjacent (1.6× on average) and in tumor (3.0× on average) tissues compared to disease‐free tissues. In addition, the ratio of cytoplasmic versus nuclear EGR‐1 expression was elevated in both tumor adjacent and tumor tissues. Similarly, FAS expression was elevated in both tumor adjacent (2.7× on average) and in tumor (2.5× on average) compared to disease‐free tissues.
CONCLUSIONS
EGR‐1 and FAS expression is similarly deregulated in tumor and structurally intact adjacent prostate tissues and defines field cancerization. In cases with high suspicion of prostate cancer but negative biopsy, identification of field cancerization could help clinicians target areas for repeat biopsy. Field cancerization at surgical margins on prostatectomy specimen should also be looked at as a predictor of cancer recurrence. EGR‐1 and FAS could also serve as molecular targets for chemoprevention. Prostate 72:1159–1170, 2012. © 2011 Wiley Periodicals, Inc.</description><subject>Adenocarcinoma - genetics</subject><subject>Adenocarcinoma - metabolism</subject><subject>Adenocarcinoma - pathology</subject><subject>Adult</subject><subject>Aged</subject><subject>Cells, Cultured</subject><subject>early growth response 1</subject><subject>Early Growth Response Protein 1 - biosynthesis</subject><subject>Early Growth Response Protein 1 - genetics</subject><subject>fatty acid synthase</subject><subject>Fatty Acid Synthases - biosynthesis</subject><subject>Fatty Acid Synthases - genetics</subject><subject>field cancerization</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Prostate - metabolism</subject><subject>Prostate - pathology</subject><subject>prostate cancer</subject><subject>Prostatic Neoplasms - genetics</subject><subject>Prostatic Neoplasms - metabolism</subject><subject>Prostatic Neoplasms - pathology</subject><subject>tumor adjacent</subject><subject>Tumor Cells, Cultured</subject><issn>0270-4137</issn><issn>1097-0045</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1v1DAQhi0Eokvhwg9APiKkFH8ksXNEbXdBVC3iQ3CzZu0Jdck6i-2oDf-Af4232_bIaaSZZx7NvIS85OyIMybebuOYjoSo2-YRWXDWqYqxunlMFkwoVtVcqgPyLKUrxgrOxFNyIAQXqtPtgvw9hTjM9Gccr_MljZi2Y0hIOYXgaA85zxSsdzTNIV9CmeDNtlDJj4H6RGHIGNFRH2ieNmOk4K7AYsh0d1SGjDT7lCa89fngvC29RHuPg6MWgsXo_0AuuufkSQ9Dwhd39ZB8W55-PX5fnV2sPhy_O6tszWRT9QKgU_UaWy0Y2rbXQrNWOtl3HQJYy7lmiFJrJbUEablruoZb3mlYuwblIXm995YLf0-Ystn4ZHEYIOA4JcOZEFIp0XYFfbNHbXkmRezNNvoNxLlAZhe92X1pbqMv8Ks777TeoHtA77MuAN8D137A-T8q8-nzxZd7abXf8SnjzcMOxF-mVVI15vv5ynzkJ8vlef3DrOQ_XbOg7Q</recordid><startdate>20120801</startdate><enddate>20120801</enddate><creator>Jones, Anna C.</creator><creator>Trujillo, Kristina A.</creator><creator>Phillips, Genevieve K.</creator><creator>Fleet, Trisha M.</creator><creator>Murton, Jaclyn K.</creator><creator>Severns, Virginia</creator><creator>Shah, Satyan K.</creator><creator>Davis, Michael S.</creator><creator>Smith, Anthony Y.</creator><creator>Griffith, Jeffrey K.</creator><creator>Fischer, Edgar G.</creator><creator>Bisoffi, Marco</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</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>20120801</creationdate><title>Early growth response 1 and fatty acid synthase expression is altered in tumor adjacent prostate tissue and indicates field cancerization</title><author>Jones, Anna C. ; Trujillo, Kristina A. ; Phillips, Genevieve K. ; Fleet, Trisha M. ; Murton, Jaclyn K. ; Severns, Virginia ; Shah, Satyan K. ; Davis, Michael S. ; Smith, Anthony Y. ; Griffith, Jeffrey K. ; Fischer, Edgar G. ; Bisoffi, Marco</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4035-f2aa974be6820ec6f828063d3f99eaacc1180ee3887383a3c1d5951c198abd5e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adenocarcinoma - genetics</topic><topic>Adenocarcinoma - metabolism</topic><topic>Adenocarcinoma - pathology</topic><topic>Adult</topic><topic>Aged</topic><topic>Cells, Cultured</topic><topic>early growth response 1</topic><topic>Early Growth Response Protein 1 - biosynthesis</topic><topic>Early Growth Response Protein 1 - genetics</topic><topic>fatty acid synthase</topic><topic>Fatty Acid Synthases - biosynthesis</topic><topic>Fatty Acid Synthases - genetics</topic><topic>field cancerization</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Prostate - metabolism</topic><topic>Prostate - pathology</topic><topic>prostate cancer</topic><topic>Prostatic Neoplasms - genetics</topic><topic>Prostatic Neoplasms - metabolism</topic><topic>Prostatic Neoplasms - pathology</topic><topic>tumor adjacent</topic><topic>Tumor Cells, Cultured</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jones, Anna C.</creatorcontrib><creatorcontrib>Trujillo, Kristina A.</creatorcontrib><creatorcontrib>Phillips, Genevieve K.</creatorcontrib><creatorcontrib>Fleet, Trisha M.</creatorcontrib><creatorcontrib>Murton, Jaclyn K.</creatorcontrib><creatorcontrib>Severns, Virginia</creatorcontrib><creatorcontrib>Shah, Satyan K.</creatorcontrib><creatorcontrib>Davis, Michael S.</creatorcontrib><creatorcontrib>Smith, Anthony Y.</creatorcontrib><creatorcontrib>Griffith, Jeffrey K.</creatorcontrib><creatorcontrib>Fischer, Edgar G.</creatorcontrib><creatorcontrib>Bisoffi, Marco</creatorcontrib><collection>Istex</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>The Prostate</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jones, Anna C.</au><au>Trujillo, Kristina A.</au><au>Phillips, Genevieve K.</au><au>Fleet, Trisha M.</au><au>Murton, Jaclyn K.</au><au>Severns, Virginia</au><au>Shah, Satyan K.</au><au>Davis, Michael S.</au><au>Smith, Anthony Y.</au><au>Griffith, Jeffrey K.</au><au>Fischer, Edgar G.</au><au>Bisoffi, Marco</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Early growth response 1 and fatty acid synthase expression is altered in tumor adjacent prostate tissue and indicates field cancerization</atitle><jtitle>The Prostate</jtitle><addtitle>Prostate</addtitle><date>2012-08-01</date><risdate>2012</risdate><volume>72</volume><issue>11</issue><spage>1159</spage><epage>1170</epage><pages>1159-1170</pages><issn>0270-4137</issn><eissn>1097-0045</eissn><abstract>BACKGROUND
Field cancerization denotes the occurrence of molecular alterations in histologically normal tissues adjacent to tumors. In prostate cancer, identification of field cancerization has several potential clinical applications. However, prostate field cancerization remains ill defined. Our previous work has shown up‐regulated mRNA of the transcription factor early growth response 1 (EGR‐1) and the lipogenic enzyme fatty acid synthase (FAS) in tissues adjacent to prostate cancer.
METHODS
Immunofluorescence data were analyzed quantitatively by spectral imaging and linear unmixing to determine the protein expression levels of EGR‐1 and FAS in human cancerous, histologically normal adjacent, and disease‐free prostate tissues.
RESULTS
EGR‐1 expression was elevated in both structurally intact tumor adjacent (1.6× on average) and in tumor (3.0× on average) tissues compared to disease‐free tissues. In addition, the ratio of cytoplasmic versus nuclear EGR‐1 expression was elevated in both tumor adjacent and tumor tissues. Similarly, FAS expression was elevated in both tumor adjacent (2.7× on average) and in tumor (2.5× on average) compared to disease‐free tissues.
CONCLUSIONS
EGR‐1 and FAS expression is similarly deregulated in tumor and structurally intact adjacent prostate tissues and defines field cancerization. In cases with high suspicion of prostate cancer but negative biopsy, identification of field cancerization could help clinicians target areas for repeat biopsy. Field cancerization at surgical margins on prostatectomy specimen should also be looked at as a predictor of cancer recurrence. EGR‐1 and FAS could also serve as molecular targets for chemoprevention. Prostate 72:1159–1170, 2012. © 2011 Wiley Periodicals, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>22127986</pmid><doi>10.1002/pros.22465</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenocarcinoma - genetics Adenocarcinoma - metabolism Adenocarcinoma - pathology Adult Aged Cells, Cultured early growth response 1 Early Growth Response Protein 1 - biosynthesis Early Growth Response Protein 1 - genetics fatty acid synthase Fatty Acid Synthases - biosynthesis Fatty Acid Synthases - genetics field cancerization Humans Immunohistochemistry Male Middle Aged Prostate - metabolism Prostate - pathology prostate cancer Prostatic Neoplasms - genetics Prostatic Neoplasms - metabolism Prostatic Neoplasms - pathology tumor adjacent Tumor Cells, Cultured |
title | Early growth response 1 and fatty acid synthase expression is altered in tumor adjacent prostate tissue and indicates field cancerization |
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