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Overexpression of cyclooxygenase‐2 in multiple myeloma: Association with reduced survival
Cyclooxygenases (COX) are key enzymes in the conversion of arachidonic acid to prostaglandins. Several studies have shown a relation between angiogenesis and COX‐2 expression. Elevated expression of cyclooxygenase‐2 (COX‐2), however, has not been reported in multiple myeloma (MM) in the literature....
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Published in: | American journal of hematology 2005-11, Vol.80 (3), p.169-173 |
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creator | Cetin, Mustafa Buyukberber, Suleyman Demir, Muzaffer Sari, Ismail Sari, Ibrahim Deniz, Kemal Eser, Bulent Altuntas, Fevzi Camcı, Celalettin Öztürk, Ahmet Turgut, Burhan Vural, Özden Unal, Ali |
description | Cyclooxygenases (COX) are key enzymes in the conversion of arachidonic acid to prostaglandins. Several studies have shown a relation between angiogenesis and COX‐2 expression. Elevated expression of cyclooxygenase‐2 (COX‐2), however, has not been reported in multiple myeloma (MM) in the literature. The aim of this study is to investigate COX‐2 expression in MM as well as its correlation with prognostic factors and estimated survival rates. Immunohistochemical staining of the paraffin‐embedded bone marrow biopsy tissues (n = 51) was performed using isoform‐specific COX‐2 polyclonal antisera (Santa Cruz Biotechnology, Santa Cruz, CA). Results were correlated with recognized clinical parameters, which were retrospectively obtained from patients' files. There were 15, 19, and 17 bone marrow biopsy specimens with negative, weak–moderate, and strong COX‐2 immunostaining, respectively. According to univariate analysis, β2‐microglobulin, age, stage, COX‐2 expression, and serum lactate dehydrogenase levels were significant prognostic factors for survival in patients with multiple myeloma. COX‐2 expression, age, and serum lactate dehydrogenase levels (greater than 1× normal level) were significant prognostic factors by multivariate analysis. Kaplan–Meier overall survival estimate of those patients with negative or weak–moderate COX‐2 immunoreactivity in myeloma cells was significantly better than that of patients with strong COX‐2 immunoreactivity (log‐rank χ2 = 21,43, P < 0.001). COX‐2 overexpression was associated with reduced estimated survival. Poor prognostic factors such as LDH, age, and β2‐microglobulin were also correlated with COX‐2 expression. Potent, specific COX‐2 inhibitors showing evident antiangiogenic and antitumor effects on cancers could provide new therapeutic strategies in the treatment of MM. Am. J. Hematol. 80:169–173, 2005. © 2005 Wiley‐Liss, Inc. |
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Several studies have shown a relation between angiogenesis and COX‐2 expression. Elevated expression of cyclooxygenase‐2 (COX‐2), however, has not been reported in multiple myeloma (MM) in the literature. The aim of this study is to investigate COX‐2 expression in MM as well as its correlation with prognostic factors and estimated survival rates. Immunohistochemical staining of the paraffin‐embedded bone marrow biopsy tissues (n = 51) was performed using isoform‐specific COX‐2 polyclonal antisera (Santa Cruz Biotechnology, Santa Cruz, CA). Results were correlated with recognized clinical parameters, which were retrospectively obtained from patients' files. There were 15, 19, and 17 bone marrow biopsy specimens with negative, weak–moderate, and strong COX‐2 immunostaining, respectively. According to univariate analysis, β2‐microglobulin, age, stage, COX‐2 expression, and serum lactate dehydrogenase levels were significant prognostic factors for survival in patients with multiple myeloma. COX‐2 expression, age, and serum lactate dehydrogenase levels (greater than 1× normal level) were significant prognostic factors by multivariate analysis. Kaplan–Meier overall survival estimate of those patients with negative or weak–moderate COX‐2 immunoreactivity in myeloma cells was significantly better than that of patients with strong COX‐2 immunoreactivity (log‐rank χ2 = 21,43, P < 0.001). COX‐2 overexpression was associated with reduced estimated survival. Poor prognostic factors such as LDH, age, and β2‐microglobulin were also correlated with COX‐2 expression. Potent, specific COX‐2 inhibitors showing evident antiangiogenic and antitumor effects on cancers could provide new therapeutic strategies in the treatment of MM. Am. J. Hematol. 80:169–173, 2005. © 2005 Wiley‐Liss, Inc.</description><identifier>ISSN: 0361-8609</identifier><identifier>EISSN: 1096-8652</identifier><identifier>DOI: 10.1002/ajh.20460</identifier><identifier>PMID: 16247750</identifier><identifier>CODEN: AJHEDD</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adult ; Aged ; Analysis of Variance ; angiogenesis ; Biological and medical sciences ; COX‐2 expression ; estimated survival ; Female ; Gene Expression Regulation, Neoplastic ; Hematologic and hematopoietic diseases ; Humans ; Immunodeficiencies. Immunoglobulinopathies ; Immunoglobulinopathies ; Immunohistochemistry ; Immunopathology ; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis ; Male ; Medical sciences ; Middle Aged ; multiple myeloma ; Multiple Myeloma - diagnosis ; Multiple Myeloma - enzymology ; Multiple Myeloma - mortality ; Neoplasm Proteins - analysis ; Prognosis ; Retrospective Studies ; Risk Factors ; Survival Analysis</subject><ispartof>American journal of hematology, 2005-11, Vol.80 (3), p.169-173</ispartof><rights>Copyright © 2005 Wiley‐Liss, Inc., A Wiley Company</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4190-39681ad5e82ffc342ec9c4abb583b66a871051d48715e67ba72bc0398b94edf03</citedby><cites>FETCH-LOGICAL-c4190-39681ad5e82ffc342ec9c4abb583b66a871051d48715e67ba72bc0398b94edf03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17239551$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16247750$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cetin, Mustafa</creatorcontrib><creatorcontrib>Buyukberber, Suleyman</creatorcontrib><creatorcontrib>Demir, Muzaffer</creatorcontrib><creatorcontrib>Sari, Ismail</creatorcontrib><creatorcontrib>Sari, Ibrahim</creatorcontrib><creatorcontrib>Deniz, Kemal</creatorcontrib><creatorcontrib>Eser, Bulent</creatorcontrib><creatorcontrib>Altuntas, Fevzi</creatorcontrib><creatorcontrib>Camcı, Celalettin</creatorcontrib><creatorcontrib>Öztürk, Ahmet</creatorcontrib><creatorcontrib>Turgut, Burhan</creatorcontrib><creatorcontrib>Vural, Özden</creatorcontrib><creatorcontrib>Unal, Ali</creatorcontrib><title>Overexpression of cyclooxygenase‐2 in multiple myeloma: Association with reduced survival</title><title>American journal of hematology</title><addtitle>Am J Hematol</addtitle><description>Cyclooxygenases (COX) are key enzymes in the conversion of arachidonic acid to prostaglandins. Several studies have shown a relation between angiogenesis and COX‐2 expression. Elevated expression of cyclooxygenase‐2 (COX‐2), however, has not been reported in multiple myeloma (MM) in the literature. The aim of this study is to investigate COX‐2 expression in MM as well as its correlation with prognostic factors and estimated survival rates. Immunohistochemical staining of the paraffin‐embedded bone marrow biopsy tissues (n = 51) was performed using isoform‐specific COX‐2 polyclonal antisera (Santa Cruz Biotechnology, Santa Cruz, CA). Results were correlated with recognized clinical parameters, which were retrospectively obtained from patients' files. There were 15, 19, and 17 bone marrow biopsy specimens with negative, weak–moderate, and strong COX‐2 immunostaining, respectively. According to univariate analysis, β2‐microglobulin, age, stage, COX‐2 expression, and serum lactate dehydrogenase levels were significant prognostic factors for survival in patients with multiple myeloma. COX‐2 expression, age, and serum lactate dehydrogenase levels (greater than 1× normal level) were significant prognostic factors by multivariate analysis. Kaplan–Meier overall survival estimate of those patients with negative or weak–moderate COX‐2 immunoreactivity in myeloma cells was significantly better than that of patients with strong COX‐2 immunoreactivity (log‐rank χ2 = 21,43, P < 0.001). COX‐2 overexpression was associated with reduced estimated survival. Poor prognostic factors such as LDH, age, and β2‐microglobulin were also correlated with COX‐2 expression. Potent, specific COX‐2 inhibitors showing evident antiangiogenic and antitumor effects on cancers could provide new therapeutic strategies in the treatment of MM. Am. J. Hematol. 80:169–173, 2005. © 2005 Wiley‐Liss, Inc.</description><subject>Adult</subject><subject>Aged</subject><subject>Analysis of Variance</subject><subject>angiogenesis</subject><subject>Biological and medical sciences</subject><subject>COX‐2 expression</subject><subject>estimated survival</subject><subject>Female</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Humans</subject><subject>Immunodeficiencies. Immunoglobulinopathies</subject><subject>Immunoglobulinopathies</subject><subject>Immunohistochemistry</subject><subject>Immunopathology</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>multiple myeloma</subject><subject>Multiple Myeloma - diagnosis</subject><subject>Multiple Myeloma - enzymology</subject><subject>Multiple Myeloma - mortality</subject><subject>Neoplasm Proteins - analysis</subject><subject>Prognosis</subject><subject>Retrospective Studies</subject><subject>Risk Factors</subject><subject>Survival Analysis</subject><issn>0361-8609</issn><issn>1096-8652</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqF0L9O3EAQBvAVSgQHoeAFIjeJRHEw-9e7dCeUBCIkmqRKYa3X47Bo7T12zwfu8gh5xjxJfNxJVIhqpvjNfNJHyAmFMwrAzu393RkDoWCPzCgYNddKsndkBlzRaQdzQA5zvgegVGjYJwdUMVGWEmbk1-0aEz4tE-bsY1_EtnCjCzE-jb-xtxn__fnLCt8X3RBWfhmw6EYMsbMXxSLn6Lxdbc4e_equSNgMDpsiD2nt1zZ8IO9bGzIe7-YR-fn1y4_Lq_nN7bfry8XN3AlqYM6N0tQ2EjVrW8cFQ2ecsHUtNa-VsrqkIGkjpilRlbUtWe2AG10bgU0L_Ih83v5dpvgwYF5Vnc8OQ7A9xiFXSpeCM9BvQmpKriWjEzzdQpdizgnbapl8Z9NYUag2lVdT5dVz5ZP9uHs61B02L3LX8QQ-7YDNzoY22d75_OJKxo2Um9DzrXv0AcfXE6vF96tt9H9MgZlA</recordid><startdate>200511</startdate><enddate>200511</enddate><creator>Cetin, Mustafa</creator><creator>Buyukberber, Suleyman</creator><creator>Demir, Muzaffer</creator><creator>Sari, Ismail</creator><creator>Sari, Ibrahim</creator><creator>Deniz, Kemal</creator><creator>Eser, Bulent</creator><creator>Altuntas, Fevzi</creator><creator>Camcı, Celalettin</creator><creator>Öztürk, Ahmet</creator><creator>Turgut, Burhan</creator><creator>Vural, Özden</creator><creator>Unal, Ali</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</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>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>200511</creationdate><title>Overexpression of cyclooxygenase‐2 in multiple myeloma: Association with reduced survival</title><author>Cetin, Mustafa ; Buyukberber, Suleyman ; Demir, Muzaffer ; Sari, Ismail ; Sari, Ibrahim ; Deniz, Kemal ; Eser, Bulent ; Altuntas, Fevzi ; Camcı, Celalettin ; Öztürk, Ahmet ; Turgut, Burhan ; Vural, Özden ; Unal, Ali</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4190-39681ad5e82ffc342ec9c4abb583b66a871051d48715e67ba72bc0398b94edf03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Analysis of Variance</topic><topic>angiogenesis</topic><topic>Biological and medical sciences</topic><topic>COX‐2 expression</topic><topic>estimated survival</topic><topic>Female</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Humans</topic><topic>Immunodeficiencies. Immunoglobulinopathies</topic><topic>Immunoglobulinopathies</topic><topic>Immunohistochemistry</topic><topic>Immunopathology</topic><topic>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>multiple myeloma</topic><topic>Multiple Myeloma - diagnosis</topic><topic>Multiple Myeloma - enzymology</topic><topic>Multiple Myeloma - mortality</topic><topic>Neoplasm Proteins - analysis</topic><topic>Prognosis</topic><topic>Retrospective Studies</topic><topic>Risk Factors</topic><topic>Survival Analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cetin, Mustafa</creatorcontrib><creatorcontrib>Buyukberber, Suleyman</creatorcontrib><creatorcontrib>Demir, Muzaffer</creatorcontrib><creatorcontrib>Sari, Ismail</creatorcontrib><creatorcontrib>Sari, Ibrahim</creatorcontrib><creatorcontrib>Deniz, Kemal</creatorcontrib><creatorcontrib>Eser, Bulent</creatorcontrib><creatorcontrib>Altuntas, Fevzi</creatorcontrib><creatorcontrib>Camcı, Celalettin</creatorcontrib><creatorcontrib>Öztürk, Ahmet</creatorcontrib><creatorcontrib>Turgut, Burhan</creatorcontrib><creatorcontrib>Vural, Özden</creatorcontrib><creatorcontrib>Unal, Ali</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>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of hematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cetin, Mustafa</au><au>Buyukberber, Suleyman</au><au>Demir, Muzaffer</au><au>Sari, Ismail</au><au>Sari, Ibrahim</au><au>Deniz, Kemal</au><au>Eser, Bulent</au><au>Altuntas, Fevzi</au><au>Camcı, Celalettin</au><au>Öztürk, Ahmet</au><au>Turgut, Burhan</au><au>Vural, Özden</au><au>Unal, Ali</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Overexpression of cyclooxygenase‐2 in multiple myeloma: Association with reduced survival</atitle><jtitle>American journal of hematology</jtitle><addtitle>Am J Hematol</addtitle><date>2005-11</date><risdate>2005</risdate><volume>80</volume><issue>3</issue><spage>169</spage><epage>173</epage><pages>169-173</pages><issn>0361-8609</issn><eissn>1096-8652</eissn><coden>AJHEDD</coden><abstract>Cyclooxygenases (COX) are key enzymes in the conversion of arachidonic acid to prostaglandins. Several studies have shown a relation between angiogenesis and COX‐2 expression. Elevated expression of cyclooxygenase‐2 (COX‐2), however, has not been reported in multiple myeloma (MM) in the literature. The aim of this study is to investigate COX‐2 expression in MM as well as its correlation with prognostic factors and estimated survival rates. Immunohistochemical staining of the paraffin‐embedded bone marrow biopsy tissues (n = 51) was performed using isoform‐specific COX‐2 polyclonal antisera (Santa Cruz Biotechnology, Santa Cruz, CA). Results were correlated with recognized clinical parameters, which were retrospectively obtained from patients' files. There were 15, 19, and 17 bone marrow biopsy specimens with negative, weak–moderate, and strong COX‐2 immunostaining, respectively. According to univariate analysis, β2‐microglobulin, age, stage, COX‐2 expression, and serum lactate dehydrogenase levels were significant prognostic factors for survival in patients with multiple myeloma. COX‐2 expression, age, and serum lactate dehydrogenase levels (greater than 1× normal level) were significant prognostic factors by multivariate analysis. Kaplan–Meier overall survival estimate of those patients with negative or weak–moderate COX‐2 immunoreactivity in myeloma cells was significantly better than that of patients with strong COX‐2 immunoreactivity (log‐rank χ2 = 21,43, P < 0.001). COX‐2 overexpression was associated with reduced estimated survival. Poor prognostic factors such as LDH, age, and β2‐microglobulin were also correlated with COX‐2 expression. Potent, specific COX‐2 inhibitors showing evident antiangiogenic and antitumor effects on cancers could provide new therapeutic strategies in the treatment of MM. Am. J. Hematol. 80:169–173, 2005. © 2005 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>16247750</pmid><doi>10.1002/ajh.20460</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Analysis of Variance angiogenesis Biological and medical sciences COX‐2 expression estimated survival Female Gene Expression Regulation, Neoplastic Hematologic and hematopoietic diseases Humans Immunodeficiencies. Immunoglobulinopathies Immunoglobulinopathies Immunohistochemistry Immunopathology Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis Male Medical sciences Middle Aged multiple myeloma Multiple Myeloma - diagnosis Multiple Myeloma - enzymology Multiple Myeloma - mortality Neoplasm Proteins - analysis Prognosis Retrospective Studies Risk Factors Survival Analysis |
title | Overexpression of cyclooxygenase‐2 in multiple myeloma: Association with reduced survival |
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