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Overexpression of S100A4 is closely associated with the progression and prognosis of gastric cancer in young patients
The aim of this study was to determine the correlation of S100A4 expression with the progression, prognosis and clinical pathology of gastric cancer (GC) in young pateints. A total of 85 tumor tissues with corresponding adjacent normal tissues and 62 non-metastatic lymph nodes (LNs) with correspondi...
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Published in: | Oncology letters 2013-05, Vol.5 (5), p.1485-1490 |
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creator | LI, HUA LIU, ZIQUAN XU, CHUANXIANG CHEN, YUNYUN ZHANG, JIANWEI CUI, BO CHEN, XUEWEI AN, GAIHONG SHE, XIAOJUN LIU, HONGTAO JIANG, ZIFENG WANG, TIANHUI |
description | The aim of this study was to determine the correlation of S100A4 expression with the progression, prognosis and clinical pathology of gastric cancer (GC) in young pateints. A total of 85 tumor tissues with corresponding adjacent normal tissues and 62 non-metastatic lymph nodes (LNs) with corresponding metastatic LNs were obtained from young GC patients ( |
doi_str_mv | 10.3892/ol.2013.1220 |
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A total of 85 tumor tissues with corresponding adjacent normal tissues and 62 non-metastatic lymph nodes (LNs) with corresponding metastatic LNs were obtained from young GC patients (<40 years old) who underwent surgery between January 2001 and December 2006. The expression of S100A4 was detected by RT-PCR and immunohistochemistry. Differences in the expression of S100A4 mRNA or protein were observed among the GC tissues, matched normal gastric mucosa, non-metastatic LNs and metastatic LNs. The expression of S100A4 mRNA and protein in GC tissues and metastatic LNs was significantly higher compared with that in the matched normal gastric mucosa and non-metastatic LNs, respectively (P<0.05). The overexpression of S100A4 was significantly associated with parameters involved in tumor progression and poor prognosis, including tumor size (P=0.017), Lauren classification (P=0.002), histological classification (P= 0.010), histological differentiation (P= 0.000), Borrmann classification (P=0.020), tumor-node-metastasis (TNM) stage (P=0.000), LN metastasis (P=0.000) and distant metastasis (P=0.024). Multivariate analysis suggested that patient age (P=0.035), tumor size (P=0.002), TNM stage (P=0.001) and S100A4 upregulation (P=0.000) were independent prognostic indicators for the disease. The overexpression of S100A4 in young GC patients is significantly associated with the clinicopathological characteristics. S100A4 may be used as a biomarker to predict the progression and poor prognosis of GC in young patients.</description><identifier>ISSN: 1792-1074</identifier><identifier>EISSN: 1792-1082</identifier><identifier>DOI: 10.3892/ol.2013.1220</identifier><identifier>PMID: 23760193</identifier><language>eng</language><publisher>Greece: D.A. Spandidos</publisher><subject>Gastric cancer ; Histology ; immunohistochemistry ; Medical prognosis ; Metastasis ; Mortality ; Multivariate analysis ; Oncology ; Patients ; prognosis ; progression ; Proteins ; S100A4 ; Studies ; Surgery ; Tumors ; young patients</subject><ispartof>Oncology letters, 2013-05, Vol.5 (5), p.1485-1490</ispartof><rights>Copyright © 2013, Spandidos Publications</rights><rights>Copyright Spandidos Publications UK Ltd. 2013</rights><rights>Copyright © 2013, Spandidos Publications 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c443t-6c2038ca5e2cb9f4ce1d1e7775e5ff8573fe5459fec85d014d27e0c7f8dc36463</citedby><cites>FETCH-LOGICAL-c443t-6c2038ca5e2cb9f4ce1d1e7775e5ff8573fe5459fec85d014d27e0c7f8dc36463</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3678874/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3678874/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23760193$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>LI, HUA</creatorcontrib><creatorcontrib>LIU, ZIQUAN</creatorcontrib><creatorcontrib>XU, CHUANXIANG</creatorcontrib><creatorcontrib>CHEN, YUNYUN</creatorcontrib><creatorcontrib>ZHANG, JIANWEI</creatorcontrib><creatorcontrib>CUI, BO</creatorcontrib><creatorcontrib>CHEN, XUEWEI</creatorcontrib><creatorcontrib>AN, GAIHONG</creatorcontrib><creatorcontrib>SHE, XIAOJUN</creatorcontrib><creatorcontrib>LIU, HONGTAO</creatorcontrib><creatorcontrib>JIANG, ZIFENG</creatorcontrib><creatorcontrib>WANG, TIANHUI</creatorcontrib><title>Overexpression of S100A4 is closely associated with the progression and prognosis of gastric cancer in young patients</title><title>Oncology letters</title><addtitle>Oncol Lett</addtitle><description>The aim of this study was to determine the correlation of S100A4 expression with the progression, prognosis and clinical pathology of gastric cancer (GC) in young pateints. A total of 85 tumor tissues with corresponding adjacent normal tissues and 62 non-metastatic lymph nodes (LNs) with corresponding metastatic LNs were obtained from young GC patients (<40 years old) who underwent surgery between January 2001 and December 2006. The expression of S100A4 was detected by RT-PCR and immunohistochemistry. Differences in the expression of S100A4 mRNA or protein were observed among the GC tissues, matched normal gastric mucosa, non-metastatic LNs and metastatic LNs. The expression of S100A4 mRNA and protein in GC tissues and metastatic LNs was significantly higher compared with that in the matched normal gastric mucosa and non-metastatic LNs, respectively (P<0.05). The overexpression of S100A4 was significantly associated with parameters involved in tumor progression and poor prognosis, including tumor size (P=0.017), Lauren classification (P=0.002), histological classification (P= 0.010), histological differentiation (P= 0.000), Borrmann classification (P=0.020), tumor-node-metastasis (TNM) stage (P=0.000), LN metastasis (P=0.000) and distant metastasis (P=0.024). Multivariate analysis suggested that patient age (P=0.035), tumor size (P=0.002), TNM stage (P=0.001) and S100A4 upregulation (P=0.000) were independent prognostic indicators for the disease. The overexpression of S100A4 in young GC patients is significantly associated with the clinicopathological characteristics. S100A4 may be used as a biomarker to predict the progression and poor prognosis of GC in young patients.</description><subject>Gastric cancer</subject><subject>Histology</subject><subject>immunohistochemistry</subject><subject>Medical prognosis</subject><subject>Metastasis</subject><subject>Mortality</subject><subject>Multivariate analysis</subject><subject>Oncology</subject><subject>Patients</subject><subject>prognosis</subject><subject>progression</subject><subject>Proteins</subject><subject>S100A4</subject><subject>Studies</subject><subject>Surgery</subject><subject>Tumors</subject><subject>young patients</subject><issn>1792-1074</issn><issn>1792-1082</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNpdkd1rFDEUxQex2FL75rMEBPHB2eZzknkRSvELCn2oPoc0c2c3ZTYZc2eq-9-bcdtVGwJJyO-e3JNTVa8YXQnT8vM0rDhlYsU4p8-qE6ZbXjNq-PPDXsvj6gzxjpahGmZM86I65kI3lLXipJqv7yHDrzEDYkiRpJ7cMEovJAlI_JAQhh1xiMkHN0FHfoZpQ6YNkDGn9WORi92fc0xYqorE2uGUgyfeRQ-ZhEh2aY5rMropQJzwZXXUuwHh7GE9rb5_-vjt8kt9df356-XFVe2lFFPdeE6F8U4B97dtLz2wjoHWWoHqe6O06EFJ1fbgjeookx3XQL3uTedFIxtxWn3Y647z7RY6X97ObrBjDluXdza5YP-_iWFj1-neikYbo2URePcgkNOPGXCy24AehsFFSDNaZnijNJPCFPTNE_QuzTkWe7b8NC_tKLVQ7_eUzwkxQ39ohlG7RGrTYJdI7RJpwV__a-AAPwZYgLd7AMeSQugS_nU31FQtk0mjxG9-mKq_</recordid><startdate>20130501</startdate><enddate>20130501</enddate><creator>LI, HUA</creator><creator>LIU, ZIQUAN</creator><creator>XU, CHUANXIANG</creator><creator>CHEN, YUNYUN</creator><creator>ZHANG, JIANWEI</creator><creator>CUI, BO</creator><creator>CHEN, XUEWEI</creator><creator>AN, GAIHONG</creator><creator>SHE, XIAOJUN</creator><creator>LIU, HONGTAO</creator><creator>JIANG, ZIFENG</creator><creator>WANG, TIANHUI</creator><general>D.A. Spandidos</general><general>Spandidos Publications UK Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20130501</creationdate><title>Overexpression of S100A4 is closely associated with the progression and prognosis of gastric cancer in young patients</title><author>LI, HUA ; LIU, ZIQUAN ; XU, CHUANXIANG ; CHEN, YUNYUN ; ZHANG, JIANWEI ; CUI, BO ; CHEN, XUEWEI ; AN, GAIHONG ; SHE, XIAOJUN ; LIU, HONGTAO ; JIANG, ZIFENG ; WANG, TIANHUI</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c443t-6c2038ca5e2cb9f4ce1d1e7775e5ff8573fe5459fec85d014d27e0c7f8dc36463</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Gastric cancer</topic><topic>Histology</topic><topic>immunohistochemistry</topic><topic>Medical prognosis</topic><topic>Metastasis</topic><topic>Mortality</topic><topic>Multivariate analysis</topic><topic>Oncology</topic><topic>Patients</topic><topic>prognosis</topic><topic>progression</topic><topic>Proteins</topic><topic>S100A4</topic><topic>Studies</topic><topic>Surgery</topic><topic>Tumors</topic><topic>young patients</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>LI, HUA</creatorcontrib><creatorcontrib>LIU, ZIQUAN</creatorcontrib><creatorcontrib>XU, CHUANXIANG</creatorcontrib><creatorcontrib>CHEN, YUNYUN</creatorcontrib><creatorcontrib>ZHANG, JIANWEI</creatorcontrib><creatorcontrib>CUI, BO</creatorcontrib><creatorcontrib>CHEN, XUEWEI</creatorcontrib><creatorcontrib>AN, GAIHONG</creatorcontrib><creatorcontrib>SHE, XIAOJUN</creatorcontrib><creatorcontrib>LIU, HONGTAO</creatorcontrib><creatorcontrib>JIANG, ZIFENG</creatorcontrib><creatorcontrib>WANG, TIANHUI</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</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>British Nursing Database</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Oncology letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>LI, HUA</au><au>LIU, ZIQUAN</au><au>XU, CHUANXIANG</au><au>CHEN, YUNYUN</au><au>ZHANG, JIANWEI</au><au>CUI, BO</au><au>CHEN, XUEWEI</au><au>AN, GAIHONG</au><au>SHE, XIAOJUN</au><au>LIU, HONGTAO</au><au>JIANG, ZIFENG</au><au>WANG, TIANHUI</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Overexpression of S100A4 is closely associated with the progression and prognosis of gastric cancer in young patients</atitle><jtitle>Oncology letters</jtitle><addtitle>Oncol Lett</addtitle><date>2013-05-01</date><risdate>2013</risdate><volume>5</volume><issue>5</issue><spage>1485</spage><epage>1490</epage><pages>1485-1490</pages><issn>1792-1074</issn><eissn>1792-1082</eissn><abstract>The aim of this study was to determine the correlation of S100A4 expression with the progression, prognosis and clinical pathology of gastric cancer (GC) in young pateints. A total of 85 tumor tissues with corresponding adjacent normal tissues and 62 non-metastatic lymph nodes (LNs) with corresponding metastatic LNs were obtained from young GC patients (<40 years old) who underwent surgery between January 2001 and December 2006. The expression of S100A4 was detected by RT-PCR and immunohistochemistry. Differences in the expression of S100A4 mRNA or protein were observed among the GC tissues, matched normal gastric mucosa, non-metastatic LNs and metastatic LNs. The expression of S100A4 mRNA and protein in GC tissues and metastatic LNs was significantly higher compared with that in the matched normal gastric mucosa and non-metastatic LNs, respectively (P<0.05). The overexpression of S100A4 was significantly associated with parameters involved in tumor progression and poor prognosis, including tumor size (P=0.017), Lauren classification (P=0.002), histological classification (P= 0.010), histological differentiation (P= 0.000), Borrmann classification (P=0.020), tumor-node-metastasis (TNM) stage (P=0.000), LN metastasis (P=0.000) and distant metastasis (P=0.024). Multivariate analysis suggested that patient age (P=0.035), tumor size (P=0.002), TNM stage (P=0.001) and S100A4 upregulation (P=0.000) were independent prognostic indicators for the disease. The overexpression of S100A4 in young GC patients is significantly associated with the clinicopathological characteristics. S100A4 may be used as a biomarker to predict the progression and poor prognosis of GC in young patients.</abstract><cop>Greece</cop><pub>D.A. Spandidos</pub><pmid>23760193</pmid><doi>10.3892/ol.2013.1220</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Gastric cancer Histology immunohistochemistry Medical prognosis Metastasis Mortality Multivariate analysis Oncology Patients prognosis progression Proteins S100A4 Studies Surgery Tumors young patients |
title | Overexpression of S100A4 is closely associated with the progression and prognosis of gastric cancer in young patients |
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