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FOXF1 as an Immunohistochemical Marker of Hilar Cholangiocarcinoma or Metastatic Pancreatic Ductal Adenocarcinoma. Single Institution Experience
Cholangiocarcinoma (CCA) is a liver malignancy associated with a poor prognosis. Its main subtypes are peripheral/intrahepatic and hilar/extrahepatic CCA. Several molecular, morphological and clinical similarities between hilar/extrahepatic CCA and pancreatic ductal adenocarcinoma (PDAC) have been d...
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Published in: | Pathology oncology research 2021-04, Vol.27, p.1609756-1609756 |
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description | Cholangiocarcinoma (CCA) is a liver malignancy associated with a poor prognosis. Its main subtypes are peripheral/intrahepatic and hilar/extrahepatic CCA. Several molecular, morphological and clinical similarities between hilar/extrahepatic CCA and pancreatic ductal adenocarcinoma (PDAC) have been described. FOXF1 is a transcription factor which has been described to have prognostic significance in various tumors and it is involved in the development of bile ducts. The aim of this study is to determine occurrence of nuclear expression of FOXF1 in both subtypes of CCA and metastatic PDAC and assess its potential usefulness as a diagnostic marker. Secondary aims were to investigate the use of C-reactive protein (CRP) immunohistochemistry for diagnosing intrahepatic peripheral CCA and the significance of histological features in CCA subtypes. 32 archive specimens of CCA, combined hepatocellular carcinoma-CCA (HCC-CCA) and liver metastasis of PDAC were stained by FOXF1 and CRP immunohistochemistry and evaluated to determine histological pattern. The CCAs were classified radiologically into peripheral/intrahepatic and hilar subtype. Using Fisher exact test, we identified nuclear FOXF1 as a fairly specific (87%) but insensitive (65%) marker of hilar and extrahepatic CCA and metastatic PDAC (
= 0.005). CRP immunohistochemistry was characterized by a high sensitivity and specificity, of 79% and 88%, respectively (
= 0.001). We did not identify any histomorphological features associated with either types of CCA or metastatic PDAC. As a conclusion of novel finding, FOXF1 immunohistochemistry may be regarded as a specific but insensitive marker of hilar/extrahepatic CCA and metastatic PDAC and it may help distinguish them from peripheral CCA. |
doi_str_mv | 10.3389/pore.2021.1609756 |
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= 0.005). CRP immunohistochemistry was characterized by a high sensitivity and specificity, of 79% and 88%, respectively (
= 0.001). We did not identify any histomorphological features associated with either types of CCA or metastatic PDAC. As a conclusion of novel finding, FOXF1 immunohistochemistry may be regarded as a specific but insensitive marker of hilar/extrahepatic CCA and metastatic PDAC and it may help distinguish them from peripheral CCA.</description><identifier>ISSN: 1532-2807</identifier><identifier>ISSN: 1219-4956</identifier><identifier>EISSN: 1532-2807</identifier><identifier>DOI: 10.3389/pore.2021.1609756</identifier><identifier>PMID: 34257615</identifier><language>eng</language><publisher>Switzerland: Frontiers Media SA</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Automation ; Bile Duct Neoplasms - metabolism ; Bile Duct Neoplasms - pathology ; Bile ducts ; Biomarkers, Tumor - metabolism ; Biopsy ; Cancer ; Carcinoma, Hepatocellular - metabolism ; Carcinoma, Hepatocellular - pathology ; Carcinoma, Pancreatic Ductal - metabolism ; Carcinoma, Pancreatic Ductal - secondary ; Cholangiocarcinoma ; Female ; Follow-Up Studies ; Forkhead Transcription Factors - metabolism ; Gallbladder ; Humans ; Immunohistochemistry ; Klatskin Tumor - metabolism ; Klatskin Tumor - pathology ; Liver ; Liver cancer ; Liver Neoplasms - metabolism ; Liver Neoplasms - secondary ; Male ; Metastasis ; Middle Aged ; Morphology ; Pancreatic cancer ; Pancreatic Neoplasms ; Pancreatic Neoplasms - metabolism ; Pancreatic Neoplasms - pathology ; Prognosis ; Society Journal Archive ; Surgery ; Survival Rate ; Tumors</subject><ispartof>Pathology oncology research, 2021-04, Vol.27, p.1609756-1609756</ispartof><rights>Copyright © 2021 Hrudka, Prouzová, Mydlíková, Jedličková, Holešta, Whitley and Havlůj.</rights><rights>2021. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Copyright © 2021 Hrudka, Prouzová, Mydlíková, Jedličková, Holešta, Whitley and Havlůj. 2021 Hrudka, Prouzová, Mydlíková, Jedličková, Holešta, Whitley and Havlůj</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c427t-824d2e7e6298d76321207d30adec97037003abf19192285c7845063475c34dfb3</citedby><cites>FETCH-LOGICAL-c427t-824d2e7e6298d76321207d30adec97037003abf19192285c7845063475c34dfb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2575515071/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2575515071?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,25734,27905,27906,36993,36994,44571,53772,53774,74875</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34257615$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hrudka, Jan</creatorcontrib><creatorcontrib>Prouzová, Zuzana</creatorcontrib><creatorcontrib>Mydlíková, Katarína</creatorcontrib><creatorcontrib>Jedličková, Kristína</creatorcontrib><creatorcontrib>Holešta, Michal</creatorcontrib><creatorcontrib>Whitley, Adam</creatorcontrib><creatorcontrib>Havlůj, Lukáš</creatorcontrib><title>FOXF1 as an Immunohistochemical Marker of Hilar Cholangiocarcinoma or Metastatic Pancreatic Ductal Adenocarcinoma. Single Institution Experience</title><title>Pathology oncology research</title><addtitle>Pathol Oncol Res</addtitle><description>Cholangiocarcinoma (CCA) is a liver malignancy associated with a poor prognosis. Its main subtypes are peripheral/intrahepatic and hilar/extrahepatic CCA. Several molecular, morphological and clinical similarities between hilar/extrahepatic CCA and pancreatic ductal adenocarcinoma (PDAC) have been described. FOXF1 is a transcription factor which has been described to have prognostic significance in various tumors and it is involved in the development of bile ducts. The aim of this study is to determine occurrence of nuclear expression of FOXF1 in both subtypes of CCA and metastatic PDAC and assess its potential usefulness as a diagnostic marker. Secondary aims were to investigate the use of C-reactive protein (CRP) immunohistochemistry for diagnosing intrahepatic peripheral CCA and the significance of histological features in CCA subtypes. 32 archive specimens of CCA, combined hepatocellular carcinoma-CCA (HCC-CCA) and liver metastasis of PDAC were stained by FOXF1 and CRP immunohistochemistry and evaluated to determine histological pattern. The CCAs were classified radiologically into peripheral/intrahepatic and hilar subtype. Using Fisher exact test, we identified nuclear FOXF1 as a fairly specific (87%) but insensitive (65%) marker of hilar and extrahepatic CCA and metastatic PDAC (
= 0.005). CRP immunohistochemistry was characterized by a high sensitivity and specificity, of 79% and 88%, respectively (
= 0.001). We did not identify any histomorphological features associated with either types of CCA or metastatic PDAC. As a conclusion of novel finding, FOXF1 immunohistochemistry may be regarded as a specific but insensitive marker of hilar/extrahepatic CCA and metastatic PDAC and it may help distinguish them from peripheral CCA.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Automation</subject><subject>Bile Duct Neoplasms - metabolism</subject><subject>Bile Duct Neoplasms - pathology</subject><subject>Bile ducts</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>Biopsy</subject><subject>Cancer</subject><subject>Carcinoma, Hepatocellular - metabolism</subject><subject>Carcinoma, Hepatocellular - pathology</subject><subject>Carcinoma, Pancreatic Ductal - metabolism</subject><subject>Carcinoma, Pancreatic Ductal - secondary</subject><subject>Cholangiocarcinoma</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Forkhead Transcription Factors - metabolism</subject><subject>Gallbladder</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Klatskin Tumor - metabolism</subject><subject>Klatskin Tumor - pathology</subject><subject>Liver</subject><subject>Liver cancer</subject><subject>Liver Neoplasms - metabolism</subject><subject>Liver Neoplasms - secondary</subject><subject>Male</subject><subject>Metastasis</subject><subject>Middle Aged</subject><subject>Morphology</subject><subject>Pancreatic cancer</subject><subject>Pancreatic Neoplasms</subject><subject>Pancreatic Neoplasms - metabolism</subject><subject>Pancreatic Neoplasms - pathology</subject><subject>Prognosis</subject><subject>Society Journal Archive</subject><subject>Surgery</subject><subject>Survival Rate</subject><subject>Tumors</subject><issn>1532-2807</issn><issn>1219-4956</issn><issn>1532-2807</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNpdkU1vEzEQhq0KRD_gB_SCLHHhkuCPtb2-IFWhaSO1aqWCxM1yvLOJy64dbC9q_0V_cjc0lMLJI_mZVzPzIHRMyZTzWn_axARTRhidUkm0EnIPHVDB2YTVRL16Ue-jw5xvCSFKavkG7fOKCSWpOEAP86vvc4ptxjbgRd8PIa59LtGtoffOdvjSph-QcGzxue9swrN17GxY-ehscj7E3uKY8CUUm4st3uFrG1yC3-WXwZUx4qSB8Bef4hsfVh3gRcjFl6H4GPDp3QaSh-DgLXrd2i7Du917hL7NT7_OzicXV2eL2cnFxFVMlUnNqoaBAsl03SjJGWVENZzYBpxWhCtCuF22VFPNWC2cqitBJK-UcLxq2iU_Qp-fcjfDsofGQSjJdmaTfG_TvYnWm39_gl-bVfxlaiYZ1XwM-LgLSPHnALmY3mcH3XgdiEM2TAgqVKV1NaIf_kNv45DCuN5IqS1HFB0p-kS5FHNO0D4PQ4nZ-jZb32br2-x8jz3vX27x3PFHMH8EqHWovw</recordid><startdate>20210420</startdate><enddate>20210420</enddate><creator>Hrudka, Jan</creator><creator>Prouzová, Zuzana</creator><creator>Mydlíková, Katarína</creator><creator>Jedličková, Kristína</creator><creator>Holešta, Michal</creator><creator>Whitley, Adam</creator><creator>Havlůj, Lukáš</creator><general>Frontiers Media SA</general><general>Frontiers Media S.A</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>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20210420</creationdate><title>FOXF1 as an Immunohistochemical Marker of Hilar Cholangiocarcinoma or Metastatic Pancreatic Ductal Adenocarcinoma. Single Institution Experience</title><author>Hrudka, Jan ; Prouzová, Zuzana ; Mydlíková, Katarína ; Jedličková, Kristína ; Holešta, Michal ; Whitley, Adam ; Havlůj, Lukáš</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c427t-824d2e7e6298d76321207d30adec97037003abf19192285c7845063475c34dfb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Automation</topic><topic>Bile Duct Neoplasms - metabolism</topic><topic>Bile Duct Neoplasms - pathology</topic><topic>Bile ducts</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>Biopsy</topic><topic>Cancer</topic><topic>Carcinoma, Hepatocellular - metabolism</topic><topic>Carcinoma, Hepatocellular - pathology</topic><topic>Carcinoma, Pancreatic Ductal - metabolism</topic><topic>Carcinoma, Pancreatic Ductal - secondary</topic><topic>Cholangiocarcinoma</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Forkhead Transcription Factors - metabolism</topic><topic>Gallbladder</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Klatskin Tumor - metabolism</topic><topic>Klatskin Tumor - pathology</topic><topic>Liver</topic><topic>Liver cancer</topic><topic>Liver Neoplasms - metabolism</topic><topic>Liver Neoplasms - secondary</topic><topic>Male</topic><topic>Metastasis</topic><topic>Middle Aged</topic><topic>Morphology</topic><topic>Pancreatic cancer</topic><topic>Pancreatic Neoplasms</topic><topic>Pancreatic Neoplasms - metabolism</topic><topic>Pancreatic Neoplasms - pathology</topic><topic>Prognosis</topic><topic>Society Journal Archive</topic><topic>Surgery</topic><topic>Survival Rate</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hrudka, Jan</creatorcontrib><creatorcontrib>Prouzová, Zuzana</creatorcontrib><creatorcontrib>Mydlíková, Katarína</creatorcontrib><creatorcontrib>Jedličková, Kristína</creatorcontrib><creatorcontrib>Holešta, Michal</creatorcontrib><creatorcontrib>Whitley, Adam</creatorcontrib><creatorcontrib>Havlůj, Lukáš</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Pathology oncology research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hrudka, Jan</au><au>Prouzová, Zuzana</au><au>Mydlíková, Katarína</au><au>Jedličková, Kristína</au><au>Holešta, Michal</au><au>Whitley, Adam</au><au>Havlůj, Lukáš</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>FOXF1 as an Immunohistochemical Marker of Hilar Cholangiocarcinoma or Metastatic Pancreatic Ductal Adenocarcinoma. Single Institution Experience</atitle><jtitle>Pathology oncology research</jtitle><addtitle>Pathol Oncol Res</addtitle><date>2021-04-20</date><risdate>2021</risdate><volume>27</volume><spage>1609756</spage><epage>1609756</epage><pages>1609756-1609756</pages><issn>1532-2807</issn><issn>1219-4956</issn><eissn>1532-2807</eissn><abstract>Cholangiocarcinoma (CCA) is a liver malignancy associated with a poor prognosis. Its main subtypes are peripheral/intrahepatic and hilar/extrahepatic CCA. Several molecular, morphological and clinical similarities between hilar/extrahepatic CCA and pancreatic ductal adenocarcinoma (PDAC) have been described. FOXF1 is a transcription factor which has been described to have prognostic significance in various tumors and it is involved in the development of bile ducts. The aim of this study is to determine occurrence of nuclear expression of FOXF1 in both subtypes of CCA and metastatic PDAC and assess its potential usefulness as a diagnostic marker. Secondary aims were to investigate the use of C-reactive protein (CRP) immunohistochemistry for diagnosing intrahepatic peripheral CCA and the significance of histological features in CCA subtypes. 32 archive specimens of CCA, combined hepatocellular carcinoma-CCA (HCC-CCA) and liver metastasis of PDAC were stained by FOXF1 and CRP immunohistochemistry and evaluated to determine histological pattern. The CCAs were classified radiologically into peripheral/intrahepatic and hilar subtype. Using Fisher exact test, we identified nuclear FOXF1 as a fairly specific (87%) but insensitive (65%) marker of hilar and extrahepatic CCA and metastatic PDAC (
= 0.005). CRP immunohistochemistry was characterized by a high sensitivity and specificity, of 79% and 88%, respectively (
= 0.001). We did not identify any histomorphological features associated with either types of CCA or metastatic PDAC. As a conclusion of novel finding, FOXF1 immunohistochemistry may be regarded as a specific but insensitive marker of hilar/extrahepatic CCA and metastatic PDAC and it may help distinguish them from peripheral CCA.</abstract><cop>Switzerland</cop><pub>Frontiers Media SA</pub><pmid>34257615</pmid><doi>10.3389/pore.2021.1609756</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Aged, 80 and over Automation Bile Duct Neoplasms - metabolism Bile Duct Neoplasms - pathology Bile ducts Biomarkers, Tumor - metabolism Biopsy Cancer Carcinoma, Hepatocellular - metabolism Carcinoma, Hepatocellular - pathology Carcinoma, Pancreatic Ductal - metabolism Carcinoma, Pancreatic Ductal - secondary Cholangiocarcinoma Female Follow-Up Studies Forkhead Transcription Factors - metabolism Gallbladder Humans Immunohistochemistry Klatskin Tumor - metabolism Klatskin Tumor - pathology Liver Liver cancer Liver Neoplasms - metabolism Liver Neoplasms - secondary Male Metastasis Middle Aged Morphology Pancreatic cancer Pancreatic Neoplasms Pancreatic Neoplasms - metabolism Pancreatic Neoplasms - pathology Prognosis Society Journal Archive Surgery Survival Rate Tumors |
title | FOXF1 as an Immunohistochemical Marker of Hilar Cholangiocarcinoma or Metastatic Pancreatic Ductal Adenocarcinoma. Single Institution Experience |
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