High cyclooxygenase-2 expression in cervical adenocarcinomas
The purpose of this study was to examine the relationships between cyclooxygenase-2 (COX-2) expression and prognostic factors in cervical carcinomas. We studied COX-2 expression in 53 women with cervical cancers, including 35 squamous cell carcinomas (SCCs), 1 adenosquamous cell carcinoma (ASCC), an...
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Veröffentlicht in: | Gynecologic oncology 2003-03, Vol.88 (3), p.379-385 |
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description | The purpose of this study was to examine the relationships between cyclooxygenase-2 (COX-2) expression and prognostic factors in cervical carcinomas.
We studied COX-2 expression in 53 women with cervical cancers, including 35 squamous cell carcinomas (SCCs), 1 adenosquamous cell carcinoma (ASCC), and 17 adenocarcinomas (ACs), using commercially available polyclonal antibodies on Formalin-fixed, paraffin-embedded tissues. Normal cervical tissues were obtained as from other patients with uterine myomas treated with a total hysterectomy (
n = 16). The immunoreactivity was quantified using an immunohistochemical scoring system that approximates the use of an image analysis-based system.
Twenty-two cervical cancer tissues (41.5%), including 10 SCCs and 12 ACs, expressed COX-2 at a moderate to strong level, which significantly, differed from the negligible expression found in the control group of 16 normal cervical tissues (
P = 0.001). Different cell types showed significantly different expression levels of COX-2 (SCC at 28.6% vs AC at 70.6%,
P = 0.004). The presence of deep stromal invasion (
n = 40) showed a significant inverse relationship to COX-2 expression (32.5% vs 69.2%,
P = 0.02). The expression of COX-2 in well-differentiated carcinomas was significantly increased compared to that in moderately and poorly differentiated carcinomas (72.7% vs 33.3%, respectively,
P = 0.018).
Overexpression of COX-2 was found in both SCC and AC, but SCCs showed infrequent and low expression. These findings suggest that increased COX-2 expression may play an important role in cervical adenocarcinomas. |
doi_str_mv | 10.1016/S0090-8258(02)00066-5 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_73124163</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0090825802000665</els_id><sourcerecordid>73124163</sourcerecordid><originalsourceid>FETCH-LOGICAL-c391t-ebe8ce291f35afb7f7da746a6cf166cba9d16f57cf4a75ffc5fcfd0fabaa7f183</originalsourceid><addsrcrecordid>eNqF0M9LwzAUwPEgipvTP0HpRdFDNWmbtAVBZPgLBA_qOby-vsxI18xkG9t_b3XFHT29y-cljy9jx4JfCi7U1SvnJY-LRBbnPLngnCsVyx02FLyUsSpkucuGf2TADkL47FDKRbLPBiJRWUf4kF0_2slHhGtsnFutJ9RCoDiJaDXzFIJ1bWTbCMkvLUITQU2tQ_BoWzeFcMj2DDSBjvo5Yu_3d2_jx_j55eFpfPscY1qKeUwVFUhJKUwqwVS5yWvIMwUKjVAKKyhroYzM0WSQS2NQGjQ1N1AB5EYU6Yidbd6defe1oDDXUxuQmgZacoug81QkmVBpB-UGoncheDJ65u0U_FoLrn-y6d9s-qeJ5on-zaZlt3fSf7CoplRvt_pOHTjtAYQuhPHQog1bl6lCSJ517mbjqMuxtOR1QEstUm094VzXzv5zyjcNVIs9</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>73124163</pqid></control><display><type>article</type><title>High cyclooxygenase-2 expression in cervical adenocarcinomas</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Chen, Y.i-Jen ; Wang, Liang-Shun ; Wang, Peng-Hui ; Lai, Chiung-R.u ; Yen, Ming-Shyen ; Ng, Heung-Tat ; Yuan, Chiou-Chung</creator><creatorcontrib>Chen, Y.i-Jen ; Wang, Liang-Shun ; Wang, Peng-Hui ; Lai, Chiung-R.u ; Yen, Ming-Shyen ; Ng, Heung-Tat ; Yuan, Chiou-Chung</creatorcontrib><description>The purpose of this study was to examine the relationships between cyclooxygenase-2 (COX-2) expression and prognostic factors in cervical carcinomas.
We studied COX-2 expression in 53 women with cervical cancers, including 35 squamous cell carcinomas (SCCs), 1 adenosquamous cell carcinoma (ASCC), and 17 adenocarcinomas (ACs), using commercially available polyclonal antibodies on Formalin-fixed, paraffin-embedded tissues. Normal cervical tissues were obtained as from other patients with uterine myomas treated with a total hysterectomy (
n = 16). The immunoreactivity was quantified using an immunohistochemical scoring system that approximates the use of an image analysis-based system.
Twenty-two cervical cancer tissues (41.5%), including 10 SCCs and 12 ACs, expressed COX-2 at a moderate to strong level, which significantly, differed from the negligible expression found in the control group of 16 normal cervical tissues (
P = 0.001). Different cell types showed significantly different expression levels of COX-2 (SCC at 28.6% vs AC at 70.6%,
P = 0.004). The presence of deep stromal invasion (
n = 40) showed a significant inverse relationship to COX-2 expression (32.5% vs 69.2%,
P = 0.02). The expression of COX-2 in well-differentiated carcinomas was significantly increased compared to that in moderately and poorly differentiated carcinomas (72.7% vs 33.3%, respectively,
P = 0.018).
Overexpression of COX-2 was found in both SCC and AC, but SCCs showed infrequent and low expression. These findings suggest that increased COX-2 expression may play an important role in cervical adenocarcinomas.</description><identifier>ISSN: 0090-8258</identifier><identifier>EISSN: 1095-6859</identifier><identifier>DOI: 10.1016/S0090-8258(02)00066-5</identifier><identifier>PMID: 12648590</identifier><identifier>CODEN: GYNOA3</identifier><language>eng</language><publisher>San Diego, CA: Elsevier Inc</publisher><subject>Adenocarcinoma ; Adenocarcinoma - enzymology ; Adenocarcinoma - pathology ; Adult ; Aged ; Aged, 80 and over ; Biological and medical sciences ; Carcinoma, Adenosquamous - enzymology ; Carcinoma, Adenosquamous - pathology ; Carcinoma, Squamous Cell - enzymology ; Carcinoma, Squamous Cell - pathology ; Cervical cancer ; Cyclooxygenase (COX-2) ; Cyclooxygenase 2 ; Female ; Female genital diseases ; Gynecology. Andrology. Obstetrics ; Humans ; Immunohistochemistry ; Isoenzymes - biosynthesis ; Lymphatic Metastasis ; Management. Prenatal diagnosis ; Medical sciences ; Membrane Proteins ; Middle Aged ; Neoplasm Invasiveness ; Neoplasm Staging ; Pregnancy. Fetus. Placenta ; Prognosis ; Prostaglandin-Endoperoxide Synthases - biosynthesis ; Squamous cell carcinoma ; Tropical medicine ; Tumors ; Uterine Cervical Neoplasms - enzymology ; Uterine Cervical Neoplasms - pathology</subject><ispartof>Gynecologic oncology, 2003-03, Vol.88 (3), p.379-385</ispartof><rights>2003 Elsevier Science (USA)</rights><rights>2003 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c391t-ebe8ce291f35afb7f7da746a6cf166cba9d16f57cf4a75ffc5fcfd0fabaa7f183</citedby><cites>FETCH-LOGICAL-c391t-ebe8ce291f35afb7f7da746a6cf166cba9d16f57cf4a75ffc5fcfd0fabaa7f183</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0090-8258(02)00066-5$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14681504$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12648590$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Y.i-Jen</creatorcontrib><creatorcontrib>Wang, Liang-Shun</creatorcontrib><creatorcontrib>Wang, Peng-Hui</creatorcontrib><creatorcontrib>Lai, Chiung-R.u</creatorcontrib><creatorcontrib>Yen, Ming-Shyen</creatorcontrib><creatorcontrib>Ng, Heung-Tat</creatorcontrib><creatorcontrib>Yuan, Chiou-Chung</creatorcontrib><title>High cyclooxygenase-2 expression in cervical adenocarcinomas</title><title>Gynecologic oncology</title><addtitle>Gynecol Oncol</addtitle><description>The purpose of this study was to examine the relationships between cyclooxygenase-2 (COX-2) expression and prognostic factors in cervical carcinomas.
We studied COX-2 expression in 53 women with cervical cancers, including 35 squamous cell carcinomas (SCCs), 1 adenosquamous cell carcinoma (ASCC), and 17 adenocarcinomas (ACs), using commercially available polyclonal antibodies on Formalin-fixed, paraffin-embedded tissues. Normal cervical tissues were obtained as from other patients with uterine myomas treated with a total hysterectomy (
n = 16). The immunoreactivity was quantified using an immunohistochemical scoring system that approximates the use of an image analysis-based system.
Twenty-two cervical cancer tissues (41.5%), including 10 SCCs and 12 ACs, expressed COX-2 at a moderate to strong level, which significantly, differed from the negligible expression found in the control group of 16 normal cervical tissues (
P = 0.001). Different cell types showed significantly different expression levels of COX-2 (SCC at 28.6% vs AC at 70.6%,
P = 0.004). The presence of deep stromal invasion (
n = 40) showed a significant inverse relationship to COX-2 expression (32.5% vs 69.2%,
P = 0.02). The expression of COX-2 in well-differentiated carcinomas was significantly increased compared to that in moderately and poorly differentiated carcinomas (72.7% vs 33.3%, respectively,
P = 0.018).
Overexpression of COX-2 was found in both SCC and AC, but SCCs showed infrequent and low expression. These findings suggest that increased COX-2 expression may play an important role in cervical adenocarcinomas.</description><subject>Adenocarcinoma</subject><subject>Adenocarcinoma - enzymology</subject><subject>Adenocarcinoma - pathology</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biological and medical sciences</subject><subject>Carcinoma, Adenosquamous - enzymology</subject><subject>Carcinoma, Adenosquamous - pathology</subject><subject>Carcinoma, Squamous Cell - enzymology</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Cervical cancer</subject><subject>Cyclooxygenase (COX-2)</subject><subject>Cyclooxygenase 2</subject><subject>Female</subject><subject>Female genital diseases</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Isoenzymes - biosynthesis</subject><subject>Lymphatic Metastasis</subject><subject>Management. Prenatal diagnosis</subject><subject>Medical sciences</subject><subject>Membrane Proteins</subject><subject>Middle Aged</subject><subject>Neoplasm Invasiveness</subject><subject>Neoplasm Staging</subject><subject>Pregnancy. Fetus. Placenta</subject><subject>Prognosis</subject><subject>Prostaglandin-Endoperoxide Synthases - biosynthesis</subject><subject>Squamous cell carcinoma</subject><subject>Tropical medicine</subject><subject>Tumors</subject><subject>Uterine Cervical Neoplasms - enzymology</subject><subject>Uterine Cervical Neoplasms - pathology</subject><issn>0090-8258</issn><issn>1095-6859</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0M9LwzAUwPEgipvTP0HpRdFDNWmbtAVBZPgLBA_qOby-vsxI18xkG9t_b3XFHT29y-cljy9jx4JfCi7U1SvnJY-LRBbnPLngnCsVyx02FLyUsSpkucuGf2TADkL47FDKRbLPBiJRWUf4kF0_2slHhGtsnFutJ9RCoDiJaDXzFIJ1bWTbCMkvLUITQU2tQ_BoWzeFcMj2DDSBjvo5Yu_3d2_jx_j55eFpfPscY1qKeUwVFUhJKUwqwVS5yWvIMwUKjVAKKyhroYzM0WSQS2NQGjQ1N1AB5EYU6Yidbd6defe1oDDXUxuQmgZacoug81QkmVBpB-UGoncheDJ65u0U_FoLrn-y6d9s-qeJ5on-zaZlt3fSf7CoplRvt_pOHTjtAYQuhPHQog1bl6lCSJ517mbjqMuxtOR1QEstUm094VzXzv5zyjcNVIs9</recordid><startdate>20030301</startdate><enddate>20030301</enddate><creator>Chen, Y.i-Jen</creator><creator>Wang, Liang-Shun</creator><creator>Wang, Peng-Hui</creator><creator>Lai, Chiung-R.u</creator><creator>Yen, Ming-Shyen</creator><creator>Ng, Heung-Tat</creator><creator>Yuan, Chiou-Chung</creator><general>Elsevier Inc</general><general>Elsevier</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>20030301</creationdate><title>High cyclooxygenase-2 expression in cervical adenocarcinomas</title><author>Chen, Y.i-Jen ; Wang, Liang-Shun ; Wang, Peng-Hui ; Lai, Chiung-R.u ; Yen, Ming-Shyen ; Ng, Heung-Tat ; Yuan, Chiou-Chung</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c391t-ebe8ce291f35afb7f7da746a6cf166cba9d16f57cf4a75ffc5fcfd0fabaa7f183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Adenocarcinoma</topic><topic>Adenocarcinoma - enzymology</topic><topic>Adenocarcinoma - pathology</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biological and medical sciences</topic><topic>Carcinoma, Adenosquamous - enzymology</topic><topic>Carcinoma, Adenosquamous - pathology</topic><topic>Carcinoma, Squamous Cell - enzymology</topic><topic>Carcinoma, Squamous Cell - pathology</topic><topic>Cervical cancer</topic><topic>Cyclooxygenase (COX-2)</topic><topic>Cyclooxygenase 2</topic><topic>Female</topic><topic>Female genital diseases</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Isoenzymes - biosynthesis</topic><topic>Lymphatic Metastasis</topic><topic>Management. Prenatal diagnosis</topic><topic>Medical sciences</topic><topic>Membrane Proteins</topic><topic>Middle Aged</topic><topic>Neoplasm Invasiveness</topic><topic>Neoplasm Staging</topic><topic>Pregnancy. Fetus. Placenta</topic><topic>Prognosis</topic><topic>Prostaglandin-Endoperoxide Synthases - biosynthesis</topic><topic>Squamous cell carcinoma</topic><topic>Tropical medicine</topic><topic>Tumors</topic><topic>Uterine Cervical Neoplasms - enzymology</topic><topic>Uterine Cervical Neoplasms - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Y.i-Jen</creatorcontrib><creatorcontrib>Wang, Liang-Shun</creatorcontrib><creatorcontrib>Wang, Peng-Hui</creatorcontrib><creatorcontrib>Lai, Chiung-R.u</creatorcontrib><creatorcontrib>Yen, Ming-Shyen</creatorcontrib><creatorcontrib>Ng, Heung-Tat</creatorcontrib><creatorcontrib>Yuan, Chiou-Chung</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>Gynecologic oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Y.i-Jen</au><au>Wang, Liang-Shun</au><au>Wang, Peng-Hui</au><au>Lai, Chiung-R.u</au><au>Yen, Ming-Shyen</au><au>Ng, Heung-Tat</au><au>Yuan, Chiou-Chung</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High cyclooxygenase-2 expression in cervical adenocarcinomas</atitle><jtitle>Gynecologic oncology</jtitle><addtitle>Gynecol Oncol</addtitle><date>2003-03-01</date><risdate>2003</risdate><volume>88</volume><issue>3</issue><spage>379</spage><epage>385</epage><pages>379-385</pages><issn>0090-8258</issn><eissn>1095-6859</eissn><coden>GYNOA3</coden><abstract>The purpose of this study was to examine the relationships between cyclooxygenase-2 (COX-2) expression and prognostic factors in cervical carcinomas.
We studied COX-2 expression in 53 women with cervical cancers, including 35 squamous cell carcinomas (SCCs), 1 adenosquamous cell carcinoma (ASCC), and 17 adenocarcinomas (ACs), using commercially available polyclonal antibodies on Formalin-fixed, paraffin-embedded tissues. Normal cervical tissues were obtained as from other patients with uterine myomas treated with a total hysterectomy (
n = 16). The immunoreactivity was quantified using an immunohistochemical scoring system that approximates the use of an image analysis-based system.
Twenty-two cervical cancer tissues (41.5%), including 10 SCCs and 12 ACs, expressed COX-2 at a moderate to strong level, which significantly, differed from the negligible expression found in the control group of 16 normal cervical tissues (
P = 0.001). Different cell types showed significantly different expression levels of COX-2 (SCC at 28.6% vs AC at 70.6%,
P = 0.004). The presence of deep stromal invasion (
n = 40) showed a significant inverse relationship to COX-2 expression (32.5% vs 69.2%,
P = 0.02). The expression of COX-2 in well-differentiated carcinomas was significantly increased compared to that in moderately and poorly differentiated carcinomas (72.7% vs 33.3%, respectively,
P = 0.018).
Overexpression of COX-2 was found in both SCC and AC, but SCCs showed infrequent and low expression. These findings suggest that increased COX-2 expression may play an important role in cervical adenocarcinomas.</abstract><cop>San Diego, CA</cop><pub>Elsevier Inc</pub><pmid>12648590</pmid><doi>10.1016/S0090-8258(02)00066-5</doi><tpages>7</tpages></addata></record> |
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subjects | Adenocarcinoma Adenocarcinoma - enzymology Adenocarcinoma - pathology Adult Aged Aged, 80 and over Biological and medical sciences Carcinoma, Adenosquamous - enzymology Carcinoma, Adenosquamous - pathology Carcinoma, Squamous Cell - enzymology Carcinoma, Squamous Cell - pathology Cervical cancer Cyclooxygenase (COX-2) Cyclooxygenase 2 Female Female genital diseases Gynecology. Andrology. Obstetrics Humans Immunohistochemistry Isoenzymes - biosynthesis Lymphatic Metastasis Management. Prenatal diagnosis Medical sciences Membrane Proteins Middle Aged Neoplasm Invasiveness Neoplasm Staging Pregnancy. Fetus. Placenta Prognosis Prostaglandin-Endoperoxide Synthases - biosynthesis Squamous cell carcinoma Tropical medicine Tumors Uterine Cervical Neoplasms - enzymology Uterine Cervical Neoplasms - pathology |
title | High cyclooxygenase-2 expression in cervical adenocarcinomas |
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