Lumican expression in advanced colorectal cancer with nodal metastasis correlates with poor prognosis
Lumican is a member of a small leucine-rich proteoglycan family, and it is reportedly overexpressed in human breast cancer. The expression of lumican in the extracellular matrix in breast cancer is associated with a high tumor grade, low estrogen receptor levels and young age. Lumican expression has...
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Veröffentlicht in: | Oncology reports 2006-12, Vol.16 (6), p.1225-1230 |
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creator | SEYA, Tomoko TANAKA, Noritake SHINJI, Seiichi YOKOI, Kimiyoshi KOIZUMI, Michihiro TERANISHI, Nobuhisa YAMASHITA, Kiyohiko TAJIRI, Takashi ISHIWATA, Toshiyuki NAITO, Zenya |
description | Lumican is a member of a small leucine-rich proteoglycan family, and it is reportedly overexpressed in human breast cancer. The expression of lumican in the extracellular matrix in breast cancer is associated with a high tumor grade, low estrogen receptor levels and young age. Lumican expression has been previously reported in colorectal cancer, but the role of lumican in the tumor is not well understood. In this study, we examined the expression and role of lumican in advanced colorectal cancer. Immunohistochemical staining was performed on 158 patients who underwent curative surgery for advanced colorectal cancer with lymph node metastasis. In the normal colorectal tissues, lumican immunoreactivity was observed in the fibroblasts and neural cells, but not in the colorectal epithelial cells. Lumican was localized in the cytoplasm of the cancer cells and its overexpression was detected in 99 of the 158 (62.7%) colorectal cancer patients. Clinicopathologically, there was no association of lumican expression with age, sex, histological typing, or venous and lymphatic invasion. However, lumican expression tended to correlate with the spread of lymph node metastasis and the depth of tumor invasion (p=0.136 and 0.135, respectively). Furthermore, the survival rate was significantly lower in patients with a high lumican expression level than in those with a low lumican expression level (p=0.048). These results indicate that lumican expression is a potential prognostic factor in patients with advanced colorectal cancer with nodal metastasis. |
doi_str_mv | 10.3892/or.16.6.1225 |
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The expression of lumican in the extracellular matrix in breast cancer is associated with a high tumor grade, low estrogen receptor levels and young age. Lumican expression has been previously reported in colorectal cancer, but the role of lumican in the tumor is not well understood. In this study, we examined the expression and role of lumican in advanced colorectal cancer. Immunohistochemical staining was performed on 158 patients who underwent curative surgery for advanced colorectal cancer with lymph node metastasis. In the normal colorectal tissues, lumican immunoreactivity was observed in the fibroblasts and neural cells, but not in the colorectal epithelial cells. Lumican was localized in the cytoplasm of the cancer cells and its overexpression was detected in 99 of the 158 (62.7%) colorectal cancer patients. Clinicopathologically, there was no association of lumican expression with age, sex, histological typing, or venous and lymphatic invasion. However, lumican expression tended to correlate with the spread of lymph node metastasis and the depth of tumor invasion (p=0.136 and 0.135, respectively). Furthermore, the survival rate was significantly lower in patients with a high lumican expression level than in those with a low lumican expression level (p=0.048). These results indicate that lumican expression is a potential prognostic factor in patients with advanced colorectal cancer with nodal metastasis.</description><identifier>ISSN: 1021-335X</identifier><identifier>EISSN: 1791-2431</identifier><identifier>DOI: 10.3892/or.16.6.1225</identifier><identifier>PMID: 17089042</identifier><language>eng</language><publisher>Athens: S.n.</publisher><subject>Adenocarcinoma - metabolism ; Adenocarcinoma - pathology ; Adult ; Aged ; Aged, 80 and over ; Biological and medical sciences ; Biomarkers, Tumor - analysis ; Chondroitin Sulfate Proteoglycans - biosynthesis ; Colorectal Neoplasms - metabolism ; Colorectal Neoplasms - pathology ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; Immunohistochemistry ; Keratan Sulfate - biosynthesis ; Lumican ; Lymphatic Metastasis - pathology ; Male ; Medical sciences ; Middle Aged ; Prognosis ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Survival Analysis ; Survival Rate ; Tumors</subject><ispartof>Oncology reports, 2006-12, Vol.16 (6), p.1225-1230</ispartof><rights>2007 INIST-CNRS</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c357t-a4f123fa0264946387f06b56f45fe6cd8e8433482b8de34e8d24563eaed0657e3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18330510$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17089042$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SEYA, Tomoko</creatorcontrib><creatorcontrib>TANAKA, Noritake</creatorcontrib><creatorcontrib>SHINJI, Seiichi</creatorcontrib><creatorcontrib>YOKOI, Kimiyoshi</creatorcontrib><creatorcontrib>KOIZUMI, Michihiro</creatorcontrib><creatorcontrib>TERANISHI, Nobuhisa</creatorcontrib><creatorcontrib>YAMASHITA, Kiyohiko</creatorcontrib><creatorcontrib>TAJIRI, Takashi</creatorcontrib><creatorcontrib>ISHIWATA, Toshiyuki</creatorcontrib><creatorcontrib>NAITO, Zenya</creatorcontrib><title>Lumican expression in advanced colorectal cancer with nodal metastasis correlates with poor prognosis</title><title>Oncology reports</title><addtitle>Oncol Rep</addtitle><description>Lumican is a member of a small leucine-rich proteoglycan family, and it is reportedly overexpressed in human breast cancer. The expression of lumican in the extracellular matrix in breast cancer is associated with a high tumor grade, low estrogen receptor levels and young age. Lumican expression has been previously reported in colorectal cancer, but the role of lumican in the tumor is not well understood. In this study, we examined the expression and role of lumican in advanced colorectal cancer. Immunohistochemical staining was performed on 158 patients who underwent curative surgery for advanced colorectal cancer with lymph node metastasis. In the normal colorectal tissues, lumican immunoreactivity was observed in the fibroblasts and neural cells, but not in the colorectal epithelial cells. Lumican was localized in the cytoplasm of the cancer cells and its overexpression was detected in 99 of the 158 (62.7%) colorectal cancer patients. Clinicopathologically, there was no association of lumican expression with age, sex, histological typing, or venous and lymphatic invasion. However, lumican expression tended to correlate with the spread of lymph node metastasis and the depth of tumor invasion (p=0.136 and 0.135, respectively). Furthermore, the survival rate was significantly lower in patients with a high lumican expression level than in those with a low lumican expression level (p=0.048). These results indicate that lumican expression is a potential prognostic factor in patients with advanced colorectal cancer with nodal metastasis.</description><subject>Adenocarcinoma - metabolism</subject><subject>Adenocarcinoma - pathology</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biological and medical sciences</subject><subject>Biomarkers, Tumor - analysis</subject><subject>Chondroitin Sulfate Proteoglycans - biosynthesis</subject><subject>Colorectal Neoplasms - metabolism</subject><subject>Colorectal Neoplasms - pathology</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Keratan Sulfate - biosynthesis</subject><subject>Lumican</subject><subject>Lymphatic Metastasis - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Prognosis</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Survival Analysis</subject><subject>Survival Rate</subject><subject>Tumors</subject><issn>1021-335X</issn><issn>1791-2431</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpF0EtLxDAUBeAgijOO7lxLNrqyNa-m6VIGXzDgRsFdyKS3GmmbmnR8_HszTGEgkHDzcS4chM4pybmq2I0POZW5zCljxQGa07KiGROcHqY3YTTjvHiboZMYPwlhJZHVMZrRkqiKCDZHsNp0zpoew-8QIEbne-x6bOpv01uosfWtD2BH02K7nQT848YP3Ps6TToYTUzHxeRCgNaMEHdg8D7gIfj33qfvU3TUmDbC2XQv0Ov93cvyMVs9Pzwtb1eZ5UU5ZkY0lPHGECZFJSRXZUPkupCNKBqQtlagBOdCsbWqgQtQNROF5GCgJrIogS_Q1S43bf7aQBx156KFtjU9-E3UUqX8ilUJXu-gDT7GAI0egutM-NOU6G2t2gdNpZZ6W2viF1PuZt1BvcdTjwlcTsBEa9ompK5c3DvFOSko4f9k44G9</recordid><startdate>20061201</startdate><enddate>20061201</enddate><creator>SEYA, Tomoko</creator><creator>TANAKA, Noritake</creator><creator>SHINJI, Seiichi</creator><creator>YOKOI, Kimiyoshi</creator><creator>KOIZUMI, Michihiro</creator><creator>TERANISHI, Nobuhisa</creator><creator>YAMASHITA, Kiyohiko</creator><creator>TAJIRI, Takashi</creator><creator>ISHIWATA, Toshiyuki</creator><creator>NAITO, Zenya</creator><general>S.n.</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>7X8</scope></search><sort><creationdate>20061201</creationdate><title>Lumican expression in advanced colorectal cancer with nodal metastasis correlates with poor prognosis</title><author>SEYA, Tomoko ; TANAKA, Noritake ; SHINJI, Seiichi ; YOKOI, Kimiyoshi ; KOIZUMI, Michihiro ; TERANISHI, Nobuhisa ; YAMASHITA, Kiyohiko ; TAJIRI, Takashi ; ISHIWATA, Toshiyuki ; NAITO, Zenya</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c357t-a4f123fa0264946387f06b56f45fe6cd8e8433482b8de34e8d24563eaed0657e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adenocarcinoma - metabolism</topic><topic>Adenocarcinoma - pathology</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor - analysis</topic><topic>Chondroitin Sulfate Proteoglycans - biosynthesis</topic><topic>Colorectal Neoplasms - metabolism</topic><topic>Colorectal Neoplasms - pathology</topic><topic>Female</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Keratan Sulfate - biosynthesis</topic><topic>Lumican</topic><topic>Lymphatic Metastasis - pathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Prognosis</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Survival Analysis</topic><topic>Survival Rate</topic><topic>Tumors</topic><toplevel>online_resources</toplevel><creatorcontrib>SEYA, Tomoko</creatorcontrib><creatorcontrib>TANAKA, Noritake</creatorcontrib><creatorcontrib>SHINJI, Seiichi</creatorcontrib><creatorcontrib>YOKOI, Kimiyoshi</creatorcontrib><creatorcontrib>KOIZUMI, Michihiro</creatorcontrib><creatorcontrib>TERANISHI, Nobuhisa</creatorcontrib><creatorcontrib>YAMASHITA, Kiyohiko</creatorcontrib><creatorcontrib>TAJIRI, Takashi</creatorcontrib><creatorcontrib>ISHIWATA, Toshiyuki</creatorcontrib><creatorcontrib>NAITO, Zenya</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>MEDLINE - Academic</collection><jtitle>Oncology reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SEYA, Tomoko</au><au>TANAKA, Noritake</au><au>SHINJI, Seiichi</au><au>YOKOI, Kimiyoshi</au><au>KOIZUMI, Michihiro</au><au>TERANISHI, Nobuhisa</au><au>YAMASHITA, Kiyohiko</au><au>TAJIRI, Takashi</au><au>ISHIWATA, Toshiyuki</au><au>NAITO, Zenya</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lumican expression in advanced colorectal cancer with nodal metastasis correlates with poor prognosis</atitle><jtitle>Oncology reports</jtitle><addtitle>Oncol Rep</addtitle><date>2006-12-01</date><risdate>2006</risdate><volume>16</volume><issue>6</issue><spage>1225</spage><epage>1230</epage><pages>1225-1230</pages><issn>1021-335X</issn><eissn>1791-2431</eissn><abstract>Lumican is a member of a small leucine-rich proteoglycan family, and it is reportedly overexpressed in human breast cancer. The expression of lumican in the extracellular matrix in breast cancer is associated with a high tumor grade, low estrogen receptor levels and young age. Lumican expression has been previously reported in colorectal cancer, but the role of lumican in the tumor is not well understood. In this study, we examined the expression and role of lumican in advanced colorectal cancer. Immunohistochemical staining was performed on 158 patients who underwent curative surgery for advanced colorectal cancer with lymph node metastasis. In the normal colorectal tissues, lumican immunoreactivity was observed in the fibroblasts and neural cells, but not in the colorectal epithelial cells. Lumican was localized in the cytoplasm of the cancer cells and its overexpression was detected in 99 of the 158 (62.7%) colorectal cancer patients. Clinicopathologically, there was no association of lumican expression with age, sex, histological typing, or venous and lymphatic invasion. However, lumican expression tended to correlate with the spread of lymph node metastasis and the depth of tumor invasion (p=0.136 and 0.135, respectively). Furthermore, the survival rate was significantly lower in patients with a high lumican expression level than in those with a low lumican expression level (p=0.048). These results indicate that lumican expression is a potential prognostic factor in patients with advanced colorectal cancer with nodal metastasis.</abstract><cop>Athens</cop><pub>S.n.</pub><pmid>17089042</pmid><doi>10.3892/or.16.6.1225</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenocarcinoma - metabolism Adenocarcinoma - pathology Adult Aged Aged, 80 and over Biological and medical sciences Biomarkers, Tumor - analysis Chondroitin Sulfate Proteoglycans - biosynthesis Colorectal Neoplasms - metabolism Colorectal Neoplasms - pathology Female Gastroenterology. Liver. Pancreas. Abdomen Humans Immunohistochemistry Keratan Sulfate - biosynthesis Lumican Lymphatic Metastasis - pathology Male Medical sciences Middle Aged Prognosis Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Survival Analysis Survival Rate Tumors |
title | Lumican expression in advanced colorectal cancer with nodal metastasis correlates with poor prognosis |
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