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Correlation of S1P1 and ERp29 expression to progression, metastasis, and poor prognosis of gallbladder adenocarcinoma
BACKGROUND: Gallbladder cancer (GBC) is one of the most aggressive malignant neoplasms with an extremely poor prognosis. Early diagnosis significantly increases the survival rate. The present study was undertaken to evaluate the diagnostic and prognostic value of sphingosine-1-phosphate receptor 1 (...
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Published in: | Hepatobiliary & pancreatic diseases international 2013-04, Vol.12 (2), p.189-195 |
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description | BACKGROUND: Gallbladder cancer (GBC) is one of the most aggressive malignant neoplasms with an extremely poor prognosis. Early diagnosis significantly increases the survival rate. The present study was undertaken to evaluate the diagnostic and prognostic value of sphingosine-1-phosphate receptor 1 (S1P1) and endoplasmic reticulum protein 29 (ERp29) in benign and malignant gallbladder lesions and to develop a possible alternative treatment for GBC. METHODS: A total of 100 gallbladder adenocarcinoma, 46 peritumoral, 30 gallbladder adenomatous, 15 gallbladder polyp and 35 chronic cholecystitis tissues were included. S1P1 and ERp29 expressions were evaluated by immunohistochemistry The correlation between S1P1 and ERp29 expression and tumor pathological features and prognosis was analyzed. RESULTS: S1P1 positive rate was significantly higher in gallbladder adenocarcinomas than that in peritumoral adenomatous, polyp, and chronic cholecystitis tissues. On the contrary, ERp29 positive rate was significantly lower in adenocarcinomas than that in peritumoral, adenomatous polyp, and chronic cholecystitis tissues. Benign lesions with positive S1P1 or negative ERp29 expression showed moderate or severe atypical hyperplasia in the gallbladder epithelium The overexpression of S1P1 or non-expression of ERp29 was significantly associated with tumor differentiation, tumor mass, lymph node metastasis, and adenocarcinoma invasion Univariate Kaplan-Meier analysis showed that the elevated S1P1 (P=0.008) or absence of ERp29 (P=0.043) was closely associated with decreased survival rate. Multivariate Cox regression analysis showed that S1P1 positive (P=0.004) or ERp29 negative (P=0.029) was an independent predictor of poor prognosis in gallbladder adenocarcinoma.CONCLUSION: S1P1 overexpression or ERp29 absence is related to the carcinogenesis and progression, and may be potential biomarkers for early detection of gallbladder adenocarcinoma. |
doi_str_mv | 10.1016/S1499-3872(13)60030-2 |
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Early diagnosis significantly increases the survival rate. The present study was undertaken to evaluate the diagnostic and prognostic value of sphingosine-1-phosphate receptor 1 (S1P1) and endoplasmic reticulum protein 29 (ERp29) in benign and malignant gallbladder lesions and to develop a possible alternative treatment for GBC. METHODS: A total of 100 gallbladder adenocarcinoma, 46 peritumoral, 30 gallbladder adenomatous, 15 gallbladder polyp and 35 chronic cholecystitis tissues were included. S1P1 and ERp29 expressions were evaluated by immunohistochemistry The correlation between S1P1 and ERp29 expression and tumor pathological features and prognosis was analyzed. RESULTS: S1P1 positive rate was significantly higher in gallbladder adenocarcinomas than that in peritumoral adenomatous, polyp, and chronic cholecystitis tissues. On the contrary, ERp29 positive rate was significantly lower in adenocarcinomas than that in peritumoral, adenomatous polyp, and chronic cholecystitis tissues. Benign lesions with positive S1P1 or negative ERp29 expression showed moderate or severe atypical hyperplasia in the gallbladder epithelium The overexpression of S1P1 or non-expression of ERp29 was significantly associated with tumor differentiation, tumor mass, lymph node metastasis, and adenocarcinoma invasion Univariate Kaplan-Meier analysis showed that the elevated S1P1 (P=0.008) or absence of ERp29 (P=0.043) was closely associated with decreased survival rate. Multivariate Cox regression analysis showed that S1P1 positive (P=0.004) or ERp29 negative (P=0.029) was an independent predictor of poor prognosis in gallbladder adenocarcinoma.CONCLUSION: S1P1 overexpression or ERp29 absence is related to the carcinogenesis and progression, and may be potential biomarkers for early detection of gallbladder adenocarcinoma.</description><identifier>ISSN: 1499-3872</identifier><identifier>DOI: 10.1016/S1499-3872(13)60030-2</identifier><identifier>PMID: 23558074</identifier><language>eng</language><publisher>Singapore: Elsevier B.V</publisher><subject>Adenocarcinoma - chemistry ; Adenocarcinoma - mortality ; Adenocarcinoma - secondary ; Adenoma - chemistry ; Adult ; Aged ; Biomarkers, Tumor - analysis ; Biopsy ; cancer ; Cell Differentiation ; Chi-Square Distribution ; cholecystitis ; Cholecystitis - metabolism ; chronic ; chronic cholecystitis ; Chronic Disease ; Down-Regulation ; Early Detection of Cancer ; Endocrinology & Metabolism ; ERp29 ; Female ; gallbladder ; gallbladder cancer ; Gallbladder Neoplasms - chemistry ; Gallbladder Neoplasms - mortality ; Gallbladder Neoplasms - pathology ; gallbladder polyp ; Gastroenterology and Hepatology ; Heat-Shock Proteins - analysis ; Humans ; Immunohistochemistry ; Kaplan-Meier Estimate ; Lymphatic Metastasis ; Male ; Middle Aged ; Multivariate Analysis ; Neoplasm Invasiveness ; polyp ; Polyps - chemistry ; Predictive Value of Tests ; Prognosis ; Proportional Hazards Models ; Receptors, Lysosphingolipid - analysis ; Risk Factors ; S1P1 ; Time Factors ; Tumor Burden ; Up-Regulation</subject><ispartof>Hepatobiliary & pancreatic diseases international, 2013-04, Vol.12 (2), p.189-195</ispartof><rights>The Editorial Board of Hepatobiliary & Pancreatic Diseases International</rights><rights>2013 The Editorial Board of Hepatobiliary & Pancreatic Diseases International</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c448t-9f5a66e7426bf22eb27984d699257a145147f2387d031e59961b3af0fda00da23</citedby><cites>FETCH-LOGICAL-c448t-9f5a66e7426bf22eb27984d699257a145147f2387d031e59961b3af0fda00da23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/89801X/89801X.jpg</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23558074$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yuan, Lian-Wen</creatorcontrib><creatorcontrib>Liu, Dong-Cai</creatorcontrib><creatorcontrib>Yang, Zhu-Lin</creatorcontrib><title>Correlation of S1P1 and ERp29 expression to progression, metastasis, and poor prognosis of gallbladder adenocarcinoma</title><title>Hepatobiliary & pancreatic diseases international</title><addtitle>Hepatobiliary & Pancreatic Diseases International</addtitle><description>BACKGROUND: Gallbladder cancer (GBC) is one of the most aggressive malignant neoplasms with an extremely poor prognosis. Early diagnosis significantly increases the survival rate. The present study was undertaken to evaluate the diagnostic and prognostic value of sphingosine-1-phosphate receptor 1 (S1P1) and endoplasmic reticulum protein 29 (ERp29) in benign and malignant gallbladder lesions and to develop a possible alternative treatment for GBC. METHODS: A total of 100 gallbladder adenocarcinoma, 46 peritumoral, 30 gallbladder adenomatous, 15 gallbladder polyp and 35 chronic cholecystitis tissues were included. S1P1 and ERp29 expressions were evaluated by immunohistochemistry The correlation between S1P1 and ERp29 expression and tumor pathological features and prognosis was analyzed. RESULTS: S1P1 positive rate was significantly higher in gallbladder adenocarcinomas than that in peritumoral adenomatous, polyp, and chronic cholecystitis tissues. On the contrary, ERp29 positive rate was significantly lower in adenocarcinomas than that in peritumoral, adenomatous polyp, and chronic cholecystitis tissues. Benign lesions with positive S1P1 or negative ERp29 expression showed moderate or severe atypical hyperplasia in the gallbladder epithelium The overexpression of S1P1 or non-expression of ERp29 was significantly associated with tumor differentiation, tumor mass, lymph node metastasis, and adenocarcinoma invasion Univariate Kaplan-Meier analysis showed that the elevated S1P1 (P=0.008) or absence of ERp29 (P=0.043) was closely associated with decreased survival rate. Multivariate Cox regression analysis showed that S1P1 positive (P=0.004) or ERp29 negative (P=0.029) was an independent predictor of poor prognosis in gallbladder adenocarcinoma.CONCLUSION: S1P1 overexpression or ERp29 absence is related to the carcinogenesis and progression, and may be potential biomarkers for early detection of gallbladder adenocarcinoma.</description><subject>Adenocarcinoma - chemistry</subject><subject>Adenocarcinoma - mortality</subject><subject>Adenocarcinoma - secondary</subject><subject>Adenoma - chemistry</subject><subject>Adult</subject><subject>Aged</subject><subject>Biomarkers, Tumor - analysis</subject><subject>Biopsy</subject><subject>cancer</subject><subject>Cell Differentiation</subject><subject>Chi-Square Distribution</subject><subject>cholecystitis</subject><subject>Cholecystitis - metabolism</subject><subject>chronic</subject><subject>chronic cholecystitis</subject><subject>Chronic Disease</subject><subject>Down-Regulation</subject><subject>Early Detection of Cancer</subject><subject>Endocrinology & Metabolism</subject><subject>ERp29</subject><subject>Female</subject><subject>gallbladder</subject><subject>gallbladder cancer</subject><subject>Gallbladder Neoplasms - chemistry</subject><subject>Gallbladder Neoplasms - mortality</subject><subject>Gallbladder Neoplasms - pathology</subject><subject>gallbladder polyp</subject><subject>Gastroenterology and Hepatology</subject><subject>Heat-Shock Proteins - analysis</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Kaplan-Meier Estimate</subject><subject>Lymphatic Metastasis</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Multivariate Analysis</subject><subject>Neoplasm Invasiveness</subject><subject>polyp</subject><subject>Polyps - chemistry</subject><subject>Predictive Value of Tests</subject><subject>Prognosis</subject><subject>Proportional Hazards Models</subject><subject>Receptors, Lysosphingolipid - analysis</subject><subject>Risk Factors</subject><subject>S1P1</subject><subject>Time Factors</subject><subject>Tumor Burden</subject><subject>Up-Regulation</subject><issn>1499-3872</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqFkF9r1jAUxnOhuLn5EZSCNxPWmX9NmxuHvGxTGEycXoc0OX3NbJMuacV9e9O-r0N2IwRCTp7zO-d5EHpN8BnBRLy_JVzKkjU1PSHsncCY4ZI-Q4eP5QP0MqU7jGnTVOIFOqCsqhpc80M0b0KM0OvJBV-ErrglX0ihvS0uvo5UFvB7jJDS8jmFYoxhu3-eFgNMOuXj0unaMIYQV4UPubawtrrv215bC7HQFnwwOhrnw6CP0fNO9wle7e8j9P3y4tvmU3l9c_V58_G6NJw3Uym7SgsBNaei7SiFltay4VZISataE14RXnc0G7SYEaikFKRlusOd1RhbTdkROtlx8173M6RJDS4Z6HvtIcxJEUY5k4TWIkurndTEkFKETo3RDTo-KILVkrJaU1ZLnLlPrSmrZcSb_Yi5HcA-dv2NOAvOdwLIRn85iCoZB96AdRHMpGxw_x3x4QnB9M47o_uf8ADpLszR5xQVUYkqvIMsDMJWwgJ4u_f2I_jtvfPbf8xlBeNZzv4APOuusg</recordid><startdate>201304</startdate><enddate>201304</enddate><creator>Yuan, Lian-Wen</creator><creator>Liu, Dong-Cai</creator><creator>Yang, Zhu-Lin</creator><general>Elsevier B.V</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</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>201304</creationdate><title>Correlation of S1P1 and ERp29 expression to progression, metastasis, and poor prognosis of gallbladder adenocarcinoma</title><author>Yuan, Lian-Wen ; Liu, Dong-Cai ; Yang, Zhu-Lin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-9f5a66e7426bf22eb27984d699257a145147f2387d031e59961b3af0fda00da23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adenocarcinoma - chemistry</topic><topic>Adenocarcinoma - mortality</topic><topic>Adenocarcinoma - secondary</topic><topic>Adenoma - chemistry</topic><topic>Adult</topic><topic>Aged</topic><topic>Biomarkers, Tumor - analysis</topic><topic>Biopsy</topic><topic>cancer</topic><topic>Cell Differentiation</topic><topic>Chi-Square Distribution</topic><topic>cholecystitis</topic><topic>Cholecystitis - metabolism</topic><topic>chronic</topic><topic>chronic cholecystitis</topic><topic>Chronic Disease</topic><topic>Down-Regulation</topic><topic>Early Detection of Cancer</topic><topic>Endocrinology & Metabolism</topic><topic>ERp29</topic><topic>Female</topic><topic>gallbladder</topic><topic>gallbladder cancer</topic><topic>Gallbladder Neoplasms - chemistry</topic><topic>Gallbladder Neoplasms - mortality</topic><topic>Gallbladder Neoplasms - pathology</topic><topic>gallbladder polyp</topic><topic>Gastroenterology and Hepatology</topic><topic>Heat-Shock Proteins - analysis</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Kaplan-Meier Estimate</topic><topic>Lymphatic Metastasis</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Multivariate Analysis</topic><topic>Neoplasm Invasiveness</topic><topic>polyp</topic><topic>Polyps - chemistry</topic><topic>Predictive Value of Tests</topic><topic>Prognosis</topic><topic>Proportional Hazards Models</topic><topic>Receptors, Lysosphingolipid - analysis</topic><topic>Risk Factors</topic><topic>S1P1</topic><topic>Time Factors</topic><topic>Tumor Burden</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yuan, Lian-Wen</creatorcontrib><creatorcontrib>Liu, Dong-Cai</creatorcontrib><creatorcontrib>Yang, Zhu-Lin</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-医药卫生</collection><collection>中文科技期刊数据库- 镜像站点</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>Hepatobiliary & pancreatic diseases international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yuan, Lian-Wen</au><au>Liu, Dong-Cai</au><au>Yang, Zhu-Lin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Correlation of S1P1 and ERp29 expression to progression, metastasis, and poor prognosis of gallbladder adenocarcinoma</atitle><jtitle>Hepatobiliary & pancreatic diseases international</jtitle><addtitle>Hepatobiliary & Pancreatic Diseases International</addtitle><date>2013-04</date><risdate>2013</risdate><volume>12</volume><issue>2</issue><spage>189</spage><epage>195</epage><pages>189-195</pages><issn>1499-3872</issn><abstract>BACKGROUND: Gallbladder cancer (GBC) is one of the most aggressive malignant neoplasms with an extremely poor prognosis. Early diagnosis significantly increases the survival rate. The present study was undertaken to evaluate the diagnostic and prognostic value of sphingosine-1-phosphate receptor 1 (S1P1) and endoplasmic reticulum protein 29 (ERp29) in benign and malignant gallbladder lesions and to develop a possible alternative treatment for GBC. METHODS: A total of 100 gallbladder adenocarcinoma, 46 peritumoral, 30 gallbladder adenomatous, 15 gallbladder polyp and 35 chronic cholecystitis tissues were included. S1P1 and ERp29 expressions were evaluated by immunohistochemistry The correlation between S1P1 and ERp29 expression and tumor pathological features and prognosis was analyzed. RESULTS: S1P1 positive rate was significantly higher in gallbladder adenocarcinomas than that in peritumoral adenomatous, polyp, and chronic cholecystitis tissues. On the contrary, ERp29 positive rate was significantly lower in adenocarcinomas than that in peritumoral, adenomatous polyp, and chronic cholecystitis tissues. Benign lesions with positive S1P1 or negative ERp29 expression showed moderate or severe atypical hyperplasia in the gallbladder epithelium The overexpression of S1P1 or non-expression of ERp29 was significantly associated with tumor differentiation, tumor mass, lymph node metastasis, and adenocarcinoma invasion Univariate Kaplan-Meier analysis showed that the elevated S1P1 (P=0.008) or absence of ERp29 (P=0.043) was closely associated with decreased survival rate. Multivariate Cox regression analysis showed that S1P1 positive (P=0.004) or ERp29 negative (P=0.029) was an independent predictor of poor prognosis in gallbladder adenocarcinoma.CONCLUSION: S1P1 overexpression or ERp29 absence is related to the carcinogenesis and progression, and may be potential biomarkers for early detection of gallbladder adenocarcinoma.</abstract><cop>Singapore</cop><pub>Elsevier B.V</pub><pmid>23558074</pmid><doi>10.1016/S1499-3872(13)60030-2</doi><tpages>7</tpages></addata></record> |
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subjects | Adenocarcinoma - chemistry Adenocarcinoma - mortality Adenocarcinoma - secondary Adenoma - chemistry Adult Aged Biomarkers, Tumor - analysis Biopsy cancer Cell Differentiation Chi-Square Distribution cholecystitis Cholecystitis - metabolism chronic chronic cholecystitis Chronic Disease Down-Regulation Early Detection of Cancer Endocrinology & Metabolism ERp29 Female gallbladder gallbladder cancer Gallbladder Neoplasms - chemistry Gallbladder Neoplasms - mortality Gallbladder Neoplasms - pathology gallbladder polyp Gastroenterology and Hepatology Heat-Shock Proteins - analysis Humans Immunohistochemistry Kaplan-Meier Estimate Lymphatic Metastasis Male Middle Aged Multivariate Analysis Neoplasm Invasiveness polyp Polyps - chemistry Predictive Value of Tests Prognosis Proportional Hazards Models Receptors, Lysosphingolipid - analysis Risk Factors S1P1 Time Factors Tumor Burden Up-Regulation |
title | Correlation of S1P1 and ERp29 expression to progression, metastasis, and poor prognosis of gallbladder adenocarcinoma |
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