HLA‐G, HLA‐E, and IDO overexpression predicts a worse survival of Tunisian patients with vulvar squamous cell carcinoma
Little is known about non‐classical HLA molecules in vulvar squamous cell carcinoma (VSCC). Because of the indoleamine‐2,3‐dioxygenase (IDO) immune tolerant role in association with HLA‐G, we evaluated the clinical and prognostic value of HLA‐G, HLA‐E, and IDO in VSCC. HLA‐G, HLA‐E, and IDO expressi...
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Veröffentlicht in: | HLA 2019-07, Vol.94 (1), p.11-24 |
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creator | Boujelbene, Nadia Ben Yahia, Hamza Babay, Wafa Gadria, Selma Zemni, Ines Azaiez, Houda Dhouioui, Sabrine Zidi, Nour Mchiri, Rim Mrad, Karima Ouzari, Hadda‐Imene Charfi, Lamia Zidi, Inès |
description | Little is known about non‐classical HLA molecules in vulvar squamous cell carcinoma (VSCC). Because of the indoleamine‐2,3‐dioxygenase (IDO) immune tolerant role in association with HLA‐G, we evaluated the clinical and prognostic value of HLA‐G, HLA‐E, and IDO in VSCC. HLA‐G, HLA‐E, and IDO expression was determined by immunohistochemistry in VSCC and associated with clinicopathological parameters and disease outcome. These three molecules were highly represented in tumoral tissues vs healthy matched vulvar tissues (P = 0.0001). Significant differences in HLA‐G expression in stages, tumor size, tumor invasion depth, and resection margins subgroups were reported (P < 0.05). At 5 years, the cumulative survival rates was of 79.8% in patients with HLA‐Glow expression vs 12.5% in those with HLA‐Ghigh expression (P < 3 × 10−5). Similarly, patients with IDOhigh expression were at a significantly reduced overall survival (OS) and disease‐free survival (DFS) rates (P = 0.011 and 0.045, respectively). The overexpression of the three molecules together worsen survival rates of VSCC patients (OS: P = 0.000038, DFS: P = 0.000085). Altogether, our results showed that HLA‐G, HLA‐E, and IDO may represent novel candidate markers for patients' prognosis and potential targets for VSCC therapy. |
doi_str_mv | 10.1111/tan.13536 |
format | Article |
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Because of the indoleamine‐2,3‐dioxygenase (IDO) immune tolerant role in association with HLA‐G, we evaluated the clinical and prognostic value of HLA‐G, HLA‐E, and IDO in VSCC. HLA‐G, HLA‐E, and IDO expression was determined by immunohistochemistry in VSCC and associated with clinicopathological parameters and disease outcome. These three molecules were highly represented in tumoral tissues vs healthy matched vulvar tissues (P = 0.0001). Significant differences in HLA‐G expression in stages, tumor size, tumor invasion depth, and resection margins subgroups were reported (P < 0.05). At 5 years, the cumulative survival rates was of 79.8% in patients with HLA‐Glow expression vs 12.5% in those with HLA‐Ghigh expression (P < 3 × 10−5). Similarly, patients with IDOhigh expression were at a significantly reduced overall survival (OS) and disease‐free survival (DFS) rates (P = 0.011 and 0.045, respectively). The overexpression of the three molecules together worsen survival rates of VSCC patients (OS: P = 0.000038, DFS: P = 0.000085). Altogether, our results showed that HLA‐G, HLA‐E, and IDO may represent novel candidate markers for patients' prognosis and potential targets for VSCC therapy.</description><identifier>ISSN: 2059-2302</identifier><identifier>EISSN: 2059-2310</identifier><identifier>DOI: 10.1111/tan.13536</identifier><identifier>PMID: 30907063</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Biomarkers, Tumor - metabolism ; Carcinoma, Squamous Cell - metabolism ; Carcinoma, Squamous Cell - mortality ; Carcinoma, Squamous Cell - pathology ; Carcinoma, Squamous Cell - surgery ; Case-Control Studies ; Female ; Follow-Up Studies ; Histocompatibility Antigens Class I - metabolism ; HLA-E Antigens ; HLA-G Antigens - metabolism ; HLA‐E ; HLA‐G ; Humans ; IDO ; Indoleamine-Pyrrole 2,3,-Dioxygenase - metabolism ; Middle Aged ; Neoplasm Invasiveness ; Prognosis ; prognostic ; survival ; Survival Rate ; vulvar cancer ; Vulvar Neoplasms - metabolism ; Vulvar Neoplasms - mortality ; Vulvar Neoplasms - pathology ; Vulvar Neoplasms - surgery</subject><ispartof>HLA, 2019-07, Vol.94 (1), p.11-24</ispartof><rights>2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd</rights><rights>2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3256-4aeff4ecfd05289c8c2521afdd8585276ffdc50b2211c7ec10b2da58624b62ca3</citedby><cites>FETCH-LOGICAL-c3256-4aeff4ecfd05289c8c2521afdd8585276ffdc50b2211c7ec10b2da58624b62ca3</cites><orcidid>0000-0002-1170-4957</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Ftan.13536$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Ftan.13536$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30907063$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Boujelbene, Nadia</creatorcontrib><creatorcontrib>Ben Yahia, Hamza</creatorcontrib><creatorcontrib>Babay, Wafa</creatorcontrib><creatorcontrib>Gadria, Selma</creatorcontrib><creatorcontrib>Zemni, Ines</creatorcontrib><creatorcontrib>Azaiez, Houda</creatorcontrib><creatorcontrib>Dhouioui, Sabrine</creatorcontrib><creatorcontrib>Zidi, Nour</creatorcontrib><creatorcontrib>Mchiri, Rim</creatorcontrib><creatorcontrib>Mrad, Karima</creatorcontrib><creatorcontrib>Ouzari, Hadda‐Imene</creatorcontrib><creatorcontrib>Charfi, Lamia</creatorcontrib><creatorcontrib>Zidi, Inès</creatorcontrib><title>HLA‐G, HLA‐E, and IDO overexpression predicts a worse survival of Tunisian patients with vulvar squamous cell carcinoma</title><title>HLA</title><addtitle>HLA</addtitle><description>Little is known about non‐classical HLA molecules in vulvar squamous cell carcinoma (VSCC). Because of the indoleamine‐2,3‐dioxygenase (IDO) immune tolerant role in association with HLA‐G, we evaluated the clinical and prognostic value of HLA‐G, HLA‐E, and IDO in VSCC. HLA‐G, HLA‐E, and IDO expression was determined by immunohistochemistry in VSCC and associated with clinicopathological parameters and disease outcome. These three molecules were highly represented in tumoral tissues vs healthy matched vulvar tissues (P = 0.0001). Significant differences in HLA‐G expression in stages, tumor size, tumor invasion depth, and resection margins subgroups were reported (P < 0.05). At 5 years, the cumulative survival rates was of 79.8% in patients with HLA‐Glow expression vs 12.5% in those with HLA‐Ghigh expression (P < 3 × 10−5). Similarly, patients with IDOhigh expression were at a significantly reduced overall survival (OS) and disease‐free survival (DFS) rates (P = 0.011 and 0.045, respectively). The overexpression of the three molecules together worsen survival rates of VSCC patients (OS: P = 0.000038, DFS: P = 0.000085). Altogether, our results showed that HLA‐G, HLA‐E, and IDO may represent novel candidate markers for patients' prognosis and potential targets for VSCC therapy.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>Carcinoma, Squamous Cell - metabolism</subject><subject>Carcinoma, Squamous Cell - mortality</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Carcinoma, Squamous Cell - surgery</subject><subject>Case-Control Studies</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Histocompatibility Antigens Class I - metabolism</subject><subject>HLA-E Antigens</subject><subject>HLA-G Antigens - metabolism</subject><subject>HLA‐E</subject><subject>HLA‐G</subject><subject>Humans</subject><subject>IDO</subject><subject>Indoleamine-Pyrrole 2,3,-Dioxygenase - metabolism</subject><subject>Middle Aged</subject><subject>Neoplasm Invasiveness</subject><subject>Prognosis</subject><subject>prognostic</subject><subject>survival</subject><subject>Survival Rate</subject><subject>vulvar cancer</subject><subject>Vulvar Neoplasms - metabolism</subject><subject>Vulvar Neoplasms - mortality</subject><subject>Vulvar Neoplasms - pathology</subject><subject>Vulvar Neoplasms - surgery</subject><issn>2059-2302</issn><issn>2059-2310</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kLtOwzAYRi0EolXpwAsgr0hNazt1moxVKW2lii5ljv74IizlUuwkpWLhEXhGngRDgA0vPsP5v-EgdE3JmPo3qaEc05CH0RnqM8KTgIWUnP8xYT00dM5khEXJjESz5BL1QpIQz2Efva6384-399UId7AcYSgl3tztcNUqq14OVvnrqsQepBG1w4CPlXUKu8a2poUcVxrvm9I4A96C2qjSW0dTP-G2yVuw2D03UFSNw0LlORZghSmrAq7QhYbcqeHPP0CP98v9Yh1sd6vNYr4NRMh4FExBaT1VQkvCWZyIWDDOKGgpYx5zNou0loKTjDFKxUwJ6lECjyM2zSImIByg225X2Mo5q3R6sKYAe0opSb8apr5h-t3Quzede2iyQsk_87eYFyadcDS5Ov2_lO7nD93kJzPefnk</recordid><startdate>201907</startdate><enddate>201907</enddate><creator>Boujelbene, Nadia</creator><creator>Ben Yahia, Hamza</creator><creator>Babay, Wafa</creator><creator>Gadria, Selma</creator><creator>Zemni, Ines</creator><creator>Azaiez, Houda</creator><creator>Dhouioui, Sabrine</creator><creator>Zidi, Nour</creator><creator>Mchiri, Rim</creator><creator>Mrad, Karima</creator><creator>Ouzari, Hadda‐Imene</creator><creator>Charfi, Lamia</creator><creator>Zidi, Inès</creator><general>Blackwell Publishing Ltd</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><orcidid>https://orcid.org/0000-0002-1170-4957</orcidid></search><sort><creationdate>201907</creationdate><title>HLA‐G, HLA‐E, and IDO overexpression predicts a worse survival of Tunisian patients with vulvar squamous cell carcinoma</title><author>Boujelbene, Nadia ; Ben Yahia, Hamza ; Babay, Wafa ; Gadria, Selma ; Zemni, Ines ; Azaiez, Houda ; Dhouioui, Sabrine ; Zidi, Nour ; Mchiri, Rim ; Mrad, Karima ; Ouzari, Hadda‐Imene ; Charfi, Lamia ; Zidi, Inès</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3256-4aeff4ecfd05289c8c2521afdd8585276ffdc50b2211c7ec10b2da58624b62ca3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>Carcinoma, Squamous Cell - metabolism</topic><topic>Carcinoma, Squamous Cell - mortality</topic><topic>Carcinoma, Squamous Cell - pathology</topic><topic>Carcinoma, Squamous Cell - surgery</topic><topic>Case-Control Studies</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Histocompatibility Antigens Class I - metabolism</topic><topic>HLA-E Antigens</topic><topic>HLA-G Antigens - metabolism</topic><topic>HLA‐E</topic><topic>HLA‐G</topic><topic>Humans</topic><topic>IDO</topic><topic>Indoleamine-Pyrrole 2,3,-Dioxygenase - metabolism</topic><topic>Middle Aged</topic><topic>Neoplasm Invasiveness</topic><topic>Prognosis</topic><topic>prognostic</topic><topic>survival</topic><topic>Survival Rate</topic><topic>vulvar cancer</topic><topic>Vulvar Neoplasms - metabolism</topic><topic>Vulvar Neoplasms - mortality</topic><topic>Vulvar Neoplasms - pathology</topic><topic>Vulvar Neoplasms - surgery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Boujelbene, Nadia</creatorcontrib><creatorcontrib>Ben Yahia, Hamza</creatorcontrib><creatorcontrib>Babay, Wafa</creatorcontrib><creatorcontrib>Gadria, Selma</creatorcontrib><creatorcontrib>Zemni, Ines</creatorcontrib><creatorcontrib>Azaiez, Houda</creatorcontrib><creatorcontrib>Dhouioui, Sabrine</creatorcontrib><creatorcontrib>Zidi, Nour</creatorcontrib><creatorcontrib>Mchiri, Rim</creatorcontrib><creatorcontrib>Mrad, Karima</creatorcontrib><creatorcontrib>Ouzari, Hadda‐Imene</creatorcontrib><creatorcontrib>Charfi, Lamia</creatorcontrib><creatorcontrib>Zidi, Inès</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>HLA</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Boujelbene, Nadia</au><au>Ben Yahia, Hamza</au><au>Babay, Wafa</au><au>Gadria, Selma</au><au>Zemni, Ines</au><au>Azaiez, Houda</au><au>Dhouioui, Sabrine</au><au>Zidi, Nour</au><au>Mchiri, Rim</au><au>Mrad, Karima</au><au>Ouzari, Hadda‐Imene</au><au>Charfi, Lamia</au><au>Zidi, Inès</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>HLA‐G, HLA‐E, and IDO overexpression predicts a worse survival of Tunisian patients with vulvar squamous cell carcinoma</atitle><jtitle>HLA</jtitle><addtitle>HLA</addtitle><date>2019-07</date><risdate>2019</risdate><volume>94</volume><issue>1</issue><spage>11</spage><epage>24</epage><pages>11-24</pages><issn>2059-2302</issn><eissn>2059-2310</eissn><abstract>Little is known about non‐classical HLA molecules in vulvar squamous cell carcinoma (VSCC). Because of the indoleamine‐2,3‐dioxygenase (IDO) immune tolerant role in association with HLA‐G, we evaluated the clinical and prognostic value of HLA‐G, HLA‐E, and IDO in VSCC. HLA‐G, HLA‐E, and IDO expression was determined by immunohistochemistry in VSCC and associated with clinicopathological parameters and disease outcome. These three molecules were highly represented in tumoral tissues vs healthy matched vulvar tissues (P = 0.0001). Significant differences in HLA‐G expression in stages, tumor size, tumor invasion depth, and resection margins subgroups were reported (P < 0.05). At 5 years, the cumulative survival rates was of 79.8% in patients with HLA‐Glow expression vs 12.5% in those with HLA‐Ghigh expression (P < 3 × 10−5). Similarly, patients with IDOhigh expression were at a significantly reduced overall survival (OS) and disease‐free survival (DFS) rates (P = 0.011 and 0.045, respectively). The overexpression of the three molecules together worsen survival rates of VSCC patients (OS: P = 0.000038, DFS: P = 0.000085). Altogether, our results showed that HLA‐G, HLA‐E, and IDO may represent novel candidate markers for patients' prognosis and potential targets for VSCC therapy.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>30907063</pmid><doi>10.1111/tan.13536</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-1170-4957</orcidid></addata></record> |
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subjects | Adult Aged Aged, 80 and over Biomarkers, Tumor - metabolism Carcinoma, Squamous Cell - metabolism Carcinoma, Squamous Cell - mortality Carcinoma, Squamous Cell - pathology Carcinoma, Squamous Cell - surgery Case-Control Studies Female Follow-Up Studies Histocompatibility Antigens Class I - metabolism HLA-E Antigens HLA-G Antigens - metabolism HLA‐E HLA‐G Humans IDO Indoleamine-Pyrrole 2,3,-Dioxygenase - metabolism Middle Aged Neoplasm Invasiveness Prognosis prognostic survival Survival Rate vulvar cancer Vulvar Neoplasms - metabolism Vulvar Neoplasms - mortality Vulvar Neoplasms - pathology Vulvar Neoplasms - surgery |
title | HLA‐G, HLA‐E, and IDO overexpression predicts a worse survival of Tunisian patients with vulvar squamous cell carcinoma |
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