Fatty acid synthase is a marker of increased risk of recurrence in endometrial carcinoma
Purpose. To explore the expression of fatty acid synthase (FAS) and human erythrocyte glucose transporter 1 (GLUT1) in endometrial carcinomas and to detect associations with clinicopathological features and prognosis. FAS and GLUT1 are two molecules involved in energy supply of normal cells. These m...
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Veröffentlicht in: | Gynecologic oncology 2004, Vol.92 (1), p.101-105 |
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container_title | Gynecologic oncology |
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creator | Sebastiani, Valeria Visca, Paolo Botti, Claudio Santeusanio, Giuseppe Galati, Gregorio Marco Piccini, Valentina Capezzone de Joannon, Barbara Di Tondo, Ugo Alo, Piero Luigi |
description | Purpose. To explore the expression of fatty acid synthase (FAS) and human erythrocyte glucose transporter 1 (GLUT1) in endometrial carcinomas and to detect associations with clinicopathological features and prognosis. FAS and GLUT1 are two molecules involved in energy supply of normal cells. These markers are overexpressed in neoplastic tissues because of their increased necessity of energy.
Methods. Ninety-five patients with endometrial carcinoma were followed-up for an average period of 5 years. FAS and GLUT1 expressions were evaluated by immunohistochemistry on formalin-fixed paraffin-embedded tissues. Staining was determined with a semiquantitative method. Negative controls were obtained from patients submitted to hysterectomy for uterine prolapse.
Results. Eighty-five cases were endometrioid, 7 were serous, and 1 was a mucinous carcinoma. Seventy-two cases (75%) were stage I, 12 (13%) were stage II, and 11 (12%) were stage III carcinomas. Sixteen (15%) carcinomas recurred. Nine patients (8%) died for cancer during the follow-up period. FAS expression was observed in 53 cases (56%). GLUT1 expression was observed in 32 (43%) cases. Statistical analysis revealed that FAS (
P = 0.04) and stage (
P = 0.001) of the disease were the only two independent predictors of recurrence. GLUT1 and other clinicopathologic parameters had no prognostic association.
Conclusions. FAS is a reliable marker of clinically aggressive endometrial carcinomas. The knowledge of FAS expression in endometrial carcinomas is an important finding that may stratify patients into selected groups and determine therapeutic approaches for patient care. |
doi_str_mv | 10.1016/j.ygyno.2003.10.027 |
format | Article |
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Methods. Ninety-five patients with endometrial carcinoma were followed-up for an average period of 5 years. FAS and GLUT1 expressions were evaluated by immunohistochemistry on formalin-fixed paraffin-embedded tissues. Staining was determined with a semiquantitative method. Negative controls were obtained from patients submitted to hysterectomy for uterine prolapse.
Results. Eighty-five cases were endometrioid, 7 were serous, and 1 was a mucinous carcinoma. Seventy-two cases (75%) were stage I, 12 (13%) were stage II, and 11 (12%) were stage III carcinomas. Sixteen (15%) carcinomas recurred. Nine patients (8%) died for cancer during the follow-up period. FAS expression was observed in 53 cases (56%). GLUT1 expression was observed in 32 (43%) cases. Statistical analysis revealed that FAS (
P = 0.04) and stage (
P = 0.001) of the disease were the only two independent predictors of recurrence. GLUT1 and other clinicopathologic parameters had no prognostic association.
Conclusions. FAS is a reliable marker of clinically aggressive endometrial carcinomas. The knowledge of FAS expression in endometrial carcinomas is an important finding that may stratify patients into selected groups and determine therapeutic approaches for patient care.</description><identifier>ISSN: 0090-8258</identifier><identifier>EISSN: 1095-6859</identifier><identifier>DOI: 10.1016/j.ygyno.2003.10.027</identifier><identifier>PMID: 14751145</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Biomarkers, Tumor - biosynthesis ; Carcinoma ; Endometrial ; Endometrial Neoplasms - enzymology ; Endometrial Neoplasms - metabolism ; Endometrial Neoplasms - pathology ; Endometrial Neoplasms - surgery ; Fatty acid synthase ; Fatty Acid Synthases - biosynthesis ; Female ; Follow-Up Studies ; Glucose Transporter Type 1 ; Humans ; Immunohistochemistry ; Middle Aged ; Monosaccharide Transport Proteins - biosynthesis ; Neoplasm Recurrence, Local - enzymology ; Neoplasm Recurrence, Local - pathology ; Neoplasm Staging ; Prognosis</subject><ispartof>Gynecologic oncology, 2004, Vol.92 (1), p.101-105</ispartof><rights>2003 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-854139678eef990ae5c70c21f7f07fc6c0bb24e9d3c5b875a4b96472010345163</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ygyno.2003.10.027$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,4025,27928,27929,27930,46000</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14751145$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sebastiani, Valeria</creatorcontrib><creatorcontrib>Visca, Paolo</creatorcontrib><creatorcontrib>Botti, Claudio</creatorcontrib><creatorcontrib>Santeusanio, Giuseppe</creatorcontrib><creatorcontrib>Galati, Gregorio Marco</creatorcontrib><creatorcontrib>Piccini, Valentina</creatorcontrib><creatorcontrib>Capezzone de Joannon, Barbara</creatorcontrib><creatorcontrib>Di Tondo, Ugo</creatorcontrib><creatorcontrib>Alo, Piero Luigi</creatorcontrib><title>Fatty acid synthase is a marker of increased risk of recurrence in endometrial carcinoma</title><title>Gynecologic oncology</title><addtitle>Gynecol Oncol</addtitle><description>Purpose. To explore the expression of fatty acid synthase (FAS) and human erythrocyte glucose transporter 1 (GLUT1) in endometrial carcinomas and to detect associations with clinicopathological features and prognosis. FAS and GLUT1 are two molecules involved in energy supply of normal cells. These markers are overexpressed in neoplastic tissues because of their increased necessity of energy.
Methods. Ninety-five patients with endometrial carcinoma were followed-up for an average period of 5 years. FAS and GLUT1 expressions were evaluated by immunohistochemistry on formalin-fixed paraffin-embedded tissues. Staining was determined with a semiquantitative method. Negative controls were obtained from patients submitted to hysterectomy for uterine prolapse.
Results. Eighty-five cases were endometrioid, 7 were serous, and 1 was a mucinous carcinoma. Seventy-two cases (75%) were stage I, 12 (13%) were stage II, and 11 (12%) were stage III carcinomas. Sixteen (15%) carcinomas recurred. Nine patients (8%) died for cancer during the follow-up period. FAS expression was observed in 53 cases (56%). GLUT1 expression was observed in 32 (43%) cases. Statistical analysis revealed that FAS (
P = 0.04) and stage (
P = 0.001) of the disease were the only two independent predictors of recurrence. GLUT1 and other clinicopathologic parameters had no prognostic association.
Conclusions. FAS is a reliable marker of clinically aggressive endometrial carcinomas. The knowledge of FAS expression in endometrial carcinomas is an important finding that may stratify patients into selected groups and determine therapeutic approaches for patient care.</description><subject>Biomarkers, Tumor - biosynthesis</subject><subject>Carcinoma</subject><subject>Endometrial</subject><subject>Endometrial Neoplasms - enzymology</subject><subject>Endometrial Neoplasms - metabolism</subject><subject>Endometrial Neoplasms - pathology</subject><subject>Endometrial Neoplasms - surgery</subject><subject>Fatty acid synthase</subject><subject>Fatty Acid Synthases - biosynthesis</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Glucose Transporter Type 1</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Middle Aged</subject><subject>Monosaccharide Transport Proteins - biosynthesis</subject><subject>Neoplasm Recurrence, Local - enzymology</subject><subject>Neoplasm Recurrence, Local - pathology</subject><subject>Neoplasm Staging</subject><subject>Prognosis</subject><issn>0090-8258</issn><issn>1095-6859</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1LxDAQhoMo7rr6CwTJyVvrpE3a5uBBxFVhwYuCt5CmU81uP9akK_Tfm7oL3jwNvDwzw_sQcskgZsCym3U8foxdHycAaUhiSPIjMmcgRZQVQh6TOYCEqEhEMSNn3q8hgMCSUzJjPBeMcTEn70s9DCPVxlbUj93wqT1S66mmrXYbdLSvqe2Mw5BX1Fm_mRKHZuccdiawHcWu6lscnNUNNdoZ2_WtPicntW48XhzmgrwtH17vn6LVy-Pz_d0qMjxhQ1QIzlKZ5QViLSVoFCYHk7A6ryGvTWagLBOOskqNKItcaF7KjOcJMEi5YFm6INf7u1vXf-3QD6q13mDT6A77nVdFaCyB8wCme9C43nuHtdo6G0qOioGahKq1-hWqJqFTGISGravD-V3ZYvW3czAYgNs9gKHkt0WnvLGTmcoGS4Oqevvvgx-mYIfc</recordid><startdate>2004</startdate><enddate>2004</enddate><creator>Sebastiani, Valeria</creator><creator>Visca, Paolo</creator><creator>Botti, Claudio</creator><creator>Santeusanio, Giuseppe</creator><creator>Galati, Gregorio Marco</creator><creator>Piccini, Valentina</creator><creator>Capezzone de Joannon, Barbara</creator><creator>Di Tondo, Ugo</creator><creator>Alo, Piero Luigi</creator><general>Elsevier Inc</general><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>2004</creationdate><title>Fatty acid synthase is a marker of increased risk of recurrence in endometrial carcinoma</title><author>Sebastiani, Valeria ; Visca, Paolo ; Botti, Claudio ; Santeusanio, Giuseppe ; Galati, Gregorio Marco ; Piccini, Valentina ; Capezzone de Joannon, Barbara ; Di Tondo, Ugo ; Alo, Piero Luigi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-854139678eef990ae5c70c21f7f07fc6c0bb24e9d3c5b875a4b96472010345163</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Biomarkers, Tumor - biosynthesis</topic><topic>Carcinoma</topic><topic>Endometrial</topic><topic>Endometrial Neoplasms - enzymology</topic><topic>Endometrial Neoplasms - metabolism</topic><topic>Endometrial Neoplasms - pathology</topic><topic>Endometrial Neoplasms - surgery</topic><topic>Fatty acid synthase</topic><topic>Fatty Acid Synthases - biosynthesis</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Glucose Transporter Type 1</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Middle Aged</topic><topic>Monosaccharide Transport Proteins - biosynthesis</topic><topic>Neoplasm Recurrence, Local - enzymology</topic><topic>Neoplasm Recurrence, Local - pathology</topic><topic>Neoplasm Staging</topic><topic>Prognosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sebastiani, Valeria</creatorcontrib><creatorcontrib>Visca, Paolo</creatorcontrib><creatorcontrib>Botti, Claudio</creatorcontrib><creatorcontrib>Santeusanio, Giuseppe</creatorcontrib><creatorcontrib>Galati, Gregorio Marco</creatorcontrib><creatorcontrib>Piccini, Valentina</creatorcontrib><creatorcontrib>Capezzone de Joannon, Barbara</creatorcontrib><creatorcontrib>Di Tondo, Ugo</creatorcontrib><creatorcontrib>Alo, Piero Luigi</creatorcontrib><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>Sebastiani, Valeria</au><au>Visca, Paolo</au><au>Botti, Claudio</au><au>Santeusanio, Giuseppe</au><au>Galati, Gregorio Marco</au><au>Piccini, Valentina</au><au>Capezzone de Joannon, Barbara</au><au>Di Tondo, Ugo</au><au>Alo, Piero Luigi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fatty acid synthase is a marker of increased risk of recurrence in endometrial carcinoma</atitle><jtitle>Gynecologic oncology</jtitle><addtitle>Gynecol Oncol</addtitle><date>2004</date><risdate>2004</risdate><volume>92</volume><issue>1</issue><spage>101</spage><epage>105</epage><pages>101-105</pages><issn>0090-8258</issn><eissn>1095-6859</eissn><abstract>Purpose. To explore the expression of fatty acid synthase (FAS) and human erythrocyte glucose transporter 1 (GLUT1) in endometrial carcinomas and to detect associations with clinicopathological features and prognosis. FAS and GLUT1 are two molecules involved in energy supply of normal cells. These markers are overexpressed in neoplastic tissues because of their increased necessity of energy.
Methods. Ninety-five patients with endometrial carcinoma were followed-up for an average period of 5 years. FAS and GLUT1 expressions were evaluated by immunohistochemistry on formalin-fixed paraffin-embedded tissues. Staining was determined with a semiquantitative method. Negative controls were obtained from patients submitted to hysterectomy for uterine prolapse.
Results. Eighty-five cases were endometrioid, 7 were serous, and 1 was a mucinous carcinoma. Seventy-two cases (75%) were stage I, 12 (13%) were stage II, and 11 (12%) were stage III carcinomas. Sixteen (15%) carcinomas recurred. Nine patients (8%) died for cancer during the follow-up period. FAS expression was observed in 53 cases (56%). GLUT1 expression was observed in 32 (43%) cases. Statistical analysis revealed that FAS (
P = 0.04) and stage (
P = 0.001) of the disease were the only two independent predictors of recurrence. GLUT1 and other clinicopathologic parameters had no prognostic association.
Conclusions. FAS is a reliable marker of clinically aggressive endometrial carcinomas. The knowledge of FAS expression in endometrial carcinomas is an important finding that may stratify patients into selected groups and determine therapeutic approaches for patient care.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>14751145</pmid><doi>10.1016/j.ygyno.2003.10.027</doi><tpages>5</tpages></addata></record> |
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subjects | Biomarkers, Tumor - biosynthesis Carcinoma Endometrial Endometrial Neoplasms - enzymology Endometrial Neoplasms - metabolism Endometrial Neoplasms - pathology Endometrial Neoplasms - surgery Fatty acid synthase Fatty Acid Synthases - biosynthesis Female Follow-Up Studies Glucose Transporter Type 1 Humans Immunohistochemistry Middle Aged Monosaccharide Transport Proteins - biosynthesis Neoplasm Recurrence, Local - enzymology Neoplasm Recurrence, Local - pathology Neoplasm Staging Prognosis |
title | Fatty acid synthase is a marker of increased risk of recurrence in endometrial carcinoma |
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