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
Hauptverfasser: Chen, Y.i-Jen, Wang, Liang-Shun, Wang, Peng-Hui, Lai, Chiung-R.u, Yen, Ming-Shyen, Ng, Heung-Tat, Yuan, Chiou-Chung
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container_end_page 385
container_issue 3
container_start_page 379
container_title Gynecologic oncology
container_volume 88
creator Chen, Y.i-Jen
Wang, Liang-Shun
Wang, Peng-Hui
Lai, Chiung-R.u
Yen, Ming-Shyen
Ng, Heung-Tat
Yuan, Chiou-Chung
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
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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. 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Prenatal diagnosis ; Medical sciences ; Membrane Proteins ; Middle Aged ; Neoplasm Invasiveness ; Neoplasm Staging ; Pregnancy. Fetus. 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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. 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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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