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Neoadjuvant Radiochemotherapy Increases Matrix Metalloproteinase Activity in Healthy Tissue in Esophageal Cancer Patients
Background Neoadjuvant radiochemotherapy (RCT) is thought to result in a favorable oncological outcome in esophageal cancer patients. Unfortunately, it also implies that adjacent healthy tissue is preoperatively exposed to the potential damaging influence of RCT. Here, the impact of preoperative RCT...
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Published in: | Annals of surgical oncology 2009-05, Vol.16 (5), p.1384-1389 |
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creator | Rieff, E. A. Hendriks, T. Rutten, H. J. T. Nieuwenhuijzen, G. A. P. Gosens, M. J. E. M. van den Brule, A. J. C. Nienhuijs, S. W. de Hingh, I. H. J. T. |
description | Background
Neoadjuvant radiochemotherapy (RCT) is thought to result in a favorable oncological outcome in esophageal cancer patients. Unfortunately, it also implies that adjacent healthy tissue is preoperatively exposed to the potential damaging influence of RCT. Here, the impact of preoperative RCT on matrix metalloproteinase (MMP) expression in healthy esophageal tissue aligned with the tumor at the time of surgery is examined.
Patients and Methods
23 patients participating in a clinical trial were randomized to either the control (
n
= 12) or the neoadjuvant RCT group (
n
= 11). In the latter group, surgery was performed 5 weeks after the last course of RCT. Full-thickness biopsies were taken from healthy esophageal tissue at the proximal border of the resection specimen and more distally next to the tumor. MMP-2 and MMP-9 activity in the samples was assessed by quantitative gelatin zymography and immunohistochemistry.
Results
In the proximal segment, the activities of the MMP-9-dimer (135 kDa) and proMMP-9 (92 kDa) were significantly increased in the RCT group as compared with the control group: 28.5 versus 3.0 (
p
= 0.025) and 87.7 versus 13.0 (
p
= 0.015) arbitrary units for 135 kDa and 92 kDa, respectively. In the distal part, RCT resulted in a significant increase of proMMP-2 (72 kDa: 35.8 versus 17.8,
p
= 0.005) and proMMP-9 (81.2 versus 23.3,
p
= 0.03).
Conclusion
In esophageal cancer patients, neoadjuvant RCT results in increased MMP expression in healthy esophageal tissue as measured at the time of surgery. Since increased levels of MMPs are associated with severe postoperative complications including anastomotic leakage this finding necessitates further clinical research. |
doi_str_mv | 10.1245/s10434-009-0365-0 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_67110774</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1673783091</sourcerecordid><originalsourceid>FETCH-LOGICAL-c369t-9425ba3791428e0b9782879cead28deefa0822b3056efd01f20cc8bda66ae7103</originalsourceid><addsrcrecordid>eNp1kVFLHDEUhYNYqrX9Ab5I8MG3qUlmJpl5lEWroFbEPoc7mTtultlkTTLS-fdm2QWh0KeEc7-ce8Ih5JSzn1xU9WXkrCqrgrG2YKWsC3ZAjnmdlUo2_DDfmWyKVsj6iHyLccUYVyWrv5Ij3gpRiYYfk_kRPfSr6R1cos_QW2-WuPZpiQE2M71zJiBEjPQBUrB_6QMmGEe_CT6hdXlCr0yy7zbN1Dp6izCm5UxfbIwTbpXr6DdLeM06XYAzGOgTJIsuxe_kywBjxB_784T8ubl-WdwW979_3S2u7gtTyjYVbSXqDkrV8hwYWdeqRjSqNQi9aHrEAVgjRJf_JXHoGR8EM6bpepASUHFWnpCLnW_O_DZhTHpto8FxBId-iloqzplSVQbP_wFXfgouZ9NCqLIWmckQ30Em-BgDDnoT7BrCrDnT21L0rhSdS9HbUvQ2wdneeOrW2H--2LeQAbEDYh65Vwyfm__v-gHmtpkg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>227352743</pqid></control><display><type>article</type><title>Neoadjuvant Radiochemotherapy Increases Matrix Metalloproteinase Activity in Healthy Tissue in Esophageal Cancer Patients</title><source>Springer Nature</source><creator>Rieff, E. A. ; Hendriks, T. ; Rutten, H. J. T. ; Nieuwenhuijzen, G. A. P. ; Gosens, M. J. E. M. ; van den Brule, A. J. C. ; Nienhuijs, S. W. ; de Hingh, I. H. J. T.</creator><creatorcontrib>Rieff, E. A. ; Hendriks, T. ; Rutten, H. J. T. ; Nieuwenhuijzen, G. A. P. ; Gosens, M. J. E. M. ; van den Brule, A. J. C. ; Nienhuijs, S. W. ; de Hingh, I. H. J. T.</creatorcontrib><description>Background
Neoadjuvant radiochemotherapy (RCT) is thought to result in a favorable oncological outcome in esophageal cancer patients. Unfortunately, it also implies that adjacent healthy tissue is preoperatively exposed to the potential damaging influence of RCT. Here, the impact of preoperative RCT on matrix metalloproteinase (MMP) expression in healthy esophageal tissue aligned with the tumor at the time of surgery is examined.
Patients and Methods
23 patients participating in a clinical trial were randomized to either the control (
n
= 12) or the neoadjuvant RCT group (
n
= 11). In the latter group, surgery was performed 5 weeks after the last course of RCT. Full-thickness biopsies were taken from healthy esophageal tissue at the proximal border of the resection specimen and more distally next to the tumor. MMP-2 and MMP-9 activity in the samples was assessed by quantitative gelatin zymography and immunohistochemistry.
Results
In the proximal segment, the activities of the MMP-9-dimer (135 kDa) and proMMP-9 (92 kDa) were significantly increased in the RCT group as compared with the control group: 28.5 versus 3.0 (
p
= 0.025) and 87.7 versus 13.0 (
p
= 0.015) arbitrary units for 135 kDa and 92 kDa, respectively. In the distal part, RCT resulted in a significant increase of proMMP-2 (72 kDa: 35.8 versus 17.8,
p
= 0.005) and proMMP-9 (81.2 versus 23.3,
p
= 0.03).
Conclusion
In esophageal cancer patients, neoadjuvant RCT results in increased MMP expression in healthy esophageal tissue as measured at the time of surgery. Since increased levels of MMPs are associated with severe postoperative complications including anastomotic leakage this finding necessitates further clinical research.</description><identifier>ISSN: 1068-9265</identifier><identifier>EISSN: 1534-4681</identifier><identifier>DOI: 10.1245/s10434-009-0365-0</identifier><identifier>PMID: 19224281</identifier><language>eng</language><publisher>New York: Springer-Verlag</publisher><subject>Aged ; Antineoplastic Combined Chemotherapy Protocols - administration & dosage ; Biopsy ; Carboplatin - administration & dosage ; Chemotherapy, Adjuvant ; Esophageal Neoplasms - metabolism ; Esophageal Neoplasms - pathology ; Esophageal Neoplasms - therapy ; Esophagus - drug effects ; Esophagus - metabolism ; Esophagus - pathology ; Esophagus - radiation effects ; Female ; Gastrointestinal Oncology ; Humans ; Immunohistochemistry ; Male ; Matrix Metalloproteinase 2 - biosynthesis ; Matrix Metalloproteinase 9 - biosynthesis ; Medicine ; Medicine & Public Health ; Middle Aged ; Neoadjuvant Therapy ; Oncology ; Paclitaxel - administration & dosage ; Radiotherapy, Adjuvant ; Surgery ; Surgical Oncology</subject><ispartof>Annals of surgical oncology, 2009-05, Vol.16 (5), p.1384-1389</ispartof><rights>Society of Surgical Oncology 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c369t-9425ba3791428e0b9782879cead28deefa0822b3056efd01f20cc8bda66ae7103</citedby><cites>FETCH-LOGICAL-c369t-9425ba3791428e0b9782879cead28deefa0822b3056efd01f20cc8bda66ae7103</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19224281$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rieff, E. A.</creatorcontrib><creatorcontrib>Hendriks, T.</creatorcontrib><creatorcontrib>Rutten, H. J. T.</creatorcontrib><creatorcontrib>Nieuwenhuijzen, G. A. P.</creatorcontrib><creatorcontrib>Gosens, M. J. E. M.</creatorcontrib><creatorcontrib>van den Brule, A. J. C.</creatorcontrib><creatorcontrib>Nienhuijs, S. W.</creatorcontrib><creatorcontrib>de Hingh, I. H. J. T.</creatorcontrib><title>Neoadjuvant Radiochemotherapy Increases Matrix Metalloproteinase Activity in Healthy Tissue in Esophageal Cancer Patients</title><title>Annals of surgical oncology</title><addtitle>Ann Surg Oncol</addtitle><addtitle>Ann Surg Oncol</addtitle><description>Background
Neoadjuvant radiochemotherapy (RCT) is thought to result in a favorable oncological outcome in esophageal cancer patients. Unfortunately, it also implies that adjacent healthy tissue is preoperatively exposed to the potential damaging influence of RCT. Here, the impact of preoperative RCT on matrix metalloproteinase (MMP) expression in healthy esophageal tissue aligned with the tumor at the time of surgery is examined.
Patients and Methods
23 patients participating in a clinical trial were randomized to either the control (
n
= 12) or the neoadjuvant RCT group (
n
= 11). In the latter group, surgery was performed 5 weeks after the last course of RCT. Full-thickness biopsies were taken from healthy esophageal tissue at the proximal border of the resection specimen and more distally next to the tumor. MMP-2 and MMP-9 activity in the samples was assessed by quantitative gelatin zymography and immunohistochemistry.
Results
In the proximal segment, the activities of the MMP-9-dimer (135 kDa) and proMMP-9 (92 kDa) were significantly increased in the RCT group as compared with the control group: 28.5 versus 3.0 (
p
= 0.025) and 87.7 versus 13.0 (
p
= 0.015) arbitrary units for 135 kDa and 92 kDa, respectively. In the distal part, RCT resulted in a significant increase of proMMP-2 (72 kDa: 35.8 versus 17.8,
p
= 0.005) and proMMP-9 (81.2 versus 23.3,
p
= 0.03).
Conclusion
In esophageal cancer patients, neoadjuvant RCT results in increased MMP expression in healthy esophageal tissue as measured at the time of surgery. Since increased levels of MMPs are associated with severe postoperative complications including anastomotic leakage this finding necessitates further clinical research.</description><subject>Aged</subject><subject>Antineoplastic Combined Chemotherapy Protocols - administration & dosage</subject><subject>Biopsy</subject><subject>Carboplatin - administration & dosage</subject><subject>Chemotherapy, Adjuvant</subject><subject>Esophageal Neoplasms - metabolism</subject><subject>Esophageal Neoplasms - pathology</subject><subject>Esophageal Neoplasms - therapy</subject><subject>Esophagus - drug effects</subject><subject>Esophagus - metabolism</subject><subject>Esophagus - pathology</subject><subject>Esophagus - radiation effects</subject><subject>Female</subject><subject>Gastrointestinal Oncology</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Male</subject><subject>Matrix Metalloproteinase 2 - biosynthesis</subject><subject>Matrix Metalloproteinase 9 - biosynthesis</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Neoadjuvant Therapy</subject><subject>Oncology</subject><subject>Paclitaxel - administration & dosage</subject><subject>Radiotherapy, Adjuvant</subject><subject>Surgery</subject><subject>Surgical Oncology</subject><issn>1068-9265</issn><issn>1534-4681</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNp1kVFLHDEUhYNYqrX9Ab5I8MG3qUlmJpl5lEWroFbEPoc7mTtultlkTTLS-fdm2QWh0KeEc7-ce8Ih5JSzn1xU9WXkrCqrgrG2YKWsC3ZAjnmdlUo2_DDfmWyKVsj6iHyLccUYVyWrv5Ij3gpRiYYfk_kRPfSr6R1cos_QW2-WuPZpiQE2M71zJiBEjPQBUrB_6QMmGEe_CT6hdXlCr0yy7zbN1Dp6izCm5UxfbIwTbpXr6DdLeM06XYAzGOgTJIsuxe_kywBjxB_784T8ubl-WdwW979_3S2u7gtTyjYVbSXqDkrV8hwYWdeqRjSqNQi9aHrEAVgjRJf_JXHoGR8EM6bpepASUHFWnpCLnW_O_DZhTHpto8FxBId-iloqzplSVQbP_wFXfgouZ9NCqLIWmckQ30Em-BgDDnoT7BrCrDnT21L0rhSdS9HbUvQ2wdneeOrW2H--2LeQAbEDYh65Vwyfm__v-gHmtpkg</recordid><startdate>20090501</startdate><enddate>20090501</enddate><creator>Rieff, E. A.</creator><creator>Hendriks, T.</creator><creator>Rutten, H. J. T.</creator><creator>Nieuwenhuijzen, G. A. P.</creator><creator>Gosens, M. J. E. M.</creator><creator>van den Brule, A. J. C.</creator><creator>Nienhuijs, S. W.</creator><creator>de Hingh, I. H. J. T.</creator><general>Springer-Verlag</general><general>Springer Nature B.V</general><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>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20090501</creationdate><title>Neoadjuvant Radiochemotherapy Increases Matrix Metalloproteinase Activity in Healthy Tissue in Esophageal Cancer Patients</title><author>Rieff, E. A. ; Hendriks, T. ; Rutten, H. J. T. ; Nieuwenhuijzen, G. A. P. ; Gosens, M. J. E. M. ; van den Brule, A. J. C. ; Nienhuijs, S. W. ; de Hingh, I. H. J. T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c369t-9425ba3791428e0b9782879cead28deefa0822b3056efd01f20cc8bda66ae7103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Aged</topic><topic>Antineoplastic Combined Chemotherapy Protocols - administration & dosage</topic><topic>Biopsy</topic><topic>Carboplatin - administration & dosage</topic><topic>Chemotherapy, Adjuvant</topic><topic>Esophageal Neoplasms - metabolism</topic><topic>Esophageal Neoplasms - pathology</topic><topic>Esophageal Neoplasms - therapy</topic><topic>Esophagus - drug effects</topic><topic>Esophagus - metabolism</topic><topic>Esophagus - pathology</topic><topic>Esophagus - radiation effects</topic><topic>Female</topic><topic>Gastrointestinal Oncology</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Male</topic><topic>Matrix Metalloproteinase 2 - biosynthesis</topic><topic>Matrix Metalloproteinase 9 - biosynthesis</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Neoadjuvant Therapy</topic><topic>Oncology</topic><topic>Paclitaxel - administration & dosage</topic><topic>Radiotherapy, Adjuvant</topic><topic>Surgery</topic><topic>Surgical Oncology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rieff, E. A.</creatorcontrib><creatorcontrib>Hendriks, T.</creatorcontrib><creatorcontrib>Rutten, H. J. T.</creatorcontrib><creatorcontrib>Nieuwenhuijzen, G. A. P.</creatorcontrib><creatorcontrib>Gosens, M. J. E. M.</creatorcontrib><creatorcontrib>van den Brule, A. J. C.</creatorcontrib><creatorcontrib>Nienhuijs, S. W.</creatorcontrib><creatorcontrib>de Hingh, I. H. J. T.</creatorcontrib><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>Oncogenes and Growth Factors 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>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Annals of surgical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rieff, E. A.</au><au>Hendriks, T.</au><au>Rutten, H. J. T.</au><au>Nieuwenhuijzen, G. A. P.</au><au>Gosens, M. J. E. M.</au><au>van den Brule, A. J. C.</au><au>Nienhuijs, S. W.</au><au>de Hingh, I. H. J. T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neoadjuvant Radiochemotherapy Increases Matrix Metalloproteinase Activity in Healthy Tissue in Esophageal Cancer Patients</atitle><jtitle>Annals of surgical oncology</jtitle><stitle>Ann Surg Oncol</stitle><addtitle>Ann Surg Oncol</addtitle><date>2009-05-01</date><risdate>2009</risdate><volume>16</volume><issue>5</issue><spage>1384</spage><epage>1389</epage><pages>1384-1389</pages><issn>1068-9265</issn><eissn>1534-4681</eissn><abstract>Background
Neoadjuvant radiochemotherapy (RCT) is thought to result in a favorable oncological outcome in esophageal cancer patients. Unfortunately, it also implies that adjacent healthy tissue is preoperatively exposed to the potential damaging influence of RCT. Here, the impact of preoperative RCT on matrix metalloproteinase (MMP) expression in healthy esophageal tissue aligned with the tumor at the time of surgery is examined.
Patients and Methods
23 patients participating in a clinical trial were randomized to either the control (
n
= 12) or the neoadjuvant RCT group (
n
= 11). In the latter group, surgery was performed 5 weeks after the last course of RCT. Full-thickness biopsies were taken from healthy esophageal tissue at the proximal border of the resection specimen and more distally next to the tumor. MMP-2 and MMP-9 activity in the samples was assessed by quantitative gelatin zymography and immunohistochemistry.
Results
In the proximal segment, the activities of the MMP-9-dimer (135 kDa) and proMMP-9 (92 kDa) were significantly increased in the RCT group as compared with the control group: 28.5 versus 3.0 (
p
= 0.025) and 87.7 versus 13.0 (
p
= 0.015) arbitrary units for 135 kDa and 92 kDa, respectively. In the distal part, RCT resulted in a significant increase of proMMP-2 (72 kDa: 35.8 versus 17.8,
p
= 0.005) and proMMP-9 (81.2 versus 23.3,
p
= 0.03).
Conclusion
In esophageal cancer patients, neoadjuvant RCT results in increased MMP expression in healthy esophageal tissue as measured at the time of surgery. Since increased levels of MMPs are associated with severe postoperative complications including anastomotic leakage this finding necessitates further clinical research.</abstract><cop>New York</cop><pub>Springer-Verlag</pub><pmid>19224281</pmid><doi>10.1245/s10434-009-0365-0</doi><tpages>6</tpages></addata></record> |
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subjects | Aged Antineoplastic Combined Chemotherapy Protocols - administration & dosage Biopsy Carboplatin - administration & dosage Chemotherapy, Adjuvant Esophageal Neoplasms - metabolism Esophageal Neoplasms - pathology Esophageal Neoplasms - therapy Esophagus - drug effects Esophagus - metabolism Esophagus - pathology Esophagus - radiation effects Female Gastrointestinal Oncology Humans Immunohistochemistry Male Matrix Metalloproteinase 2 - biosynthesis Matrix Metalloproteinase 9 - biosynthesis Medicine Medicine & Public Health Middle Aged Neoadjuvant Therapy Oncology Paclitaxel - administration & dosage Radiotherapy, Adjuvant Surgery Surgical Oncology |
title | Neoadjuvant Radiochemotherapy Increases Matrix Metalloproteinase Activity in Healthy Tissue in Esophageal Cancer Patients |
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