ASS1 Overexpression: A Hallmark of Sonic Hedgehog Hepatocellular Adenomas; Recommendations for Clinical Practice
Until recently, 10% of hepatocellular adenomas (HCAs) remained unclassified (UHCA). Among the UHCAs, the sonic hedgehog HCA (shHCA) was defined by focal deletions that fuse the promoter of Inhibin beta E chain with GLI1. Prostaglandin D2 synthase was proposed as immunomarker. In parallel, our previo...
Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
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Wiley
2020-06-01
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Series: | Hepatology Communications |
Online Access: | https://doi.org/10.1002/hep4.1514 |
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Article |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Margaux Sala Delphine Gonzales Thierry Leste‐Lasserre Nathalie Dugot‐Senant Valérie Paradis Sylvaine Di Tommaso Jean‐William Dupuy Vincent Pitard Cyril Dourthe Amedeo Sciarra Christine Sempoux Linda D. Ferrell Andrew D. Clouston Gregory Miller Mathew M. Yeh Swan Thung Annette S.H. Gouw Alberto Quaglia Jing Han Ji Huan Cathy Fan James Crawford Yasuni Nakanuma Kenichi Harada Brigitte leBail Claire Castain Nora Frulio Hervé Trillaud Laurent Possenti Jean‐Frédéric Blanc Laurence Chiche Christophe Laurent Charles Balabaud Paulette Bioulac‐Sage Anne Aurélie Raymond Frédéric Saltel |
spellingShingle |
Margaux Sala Delphine Gonzales Thierry Leste‐Lasserre Nathalie Dugot‐Senant Valérie Paradis Sylvaine Di Tommaso Jean‐William Dupuy Vincent Pitard Cyril Dourthe Amedeo Sciarra Christine Sempoux Linda D. Ferrell Andrew D. Clouston Gregory Miller Mathew M. Yeh Swan Thung Annette S.H. Gouw Alberto Quaglia Jing Han Ji Huan Cathy Fan James Crawford Yasuni Nakanuma Kenichi Harada Brigitte leBail Claire Castain Nora Frulio Hervé Trillaud Laurent Possenti Jean‐Frédéric Blanc Laurence Chiche Christophe Laurent Charles Balabaud Paulette Bioulac‐Sage Anne Aurélie Raymond Frédéric Saltel ASS1 Overexpression: A Hallmark of Sonic Hedgehog Hepatocellular Adenomas; Recommendations for Clinical Practice Hepatology Communications |
author_facet |
Margaux Sala Delphine Gonzales Thierry Leste‐Lasserre Nathalie Dugot‐Senant Valérie Paradis Sylvaine Di Tommaso Jean‐William Dupuy Vincent Pitard Cyril Dourthe Amedeo Sciarra Christine Sempoux Linda D. Ferrell Andrew D. Clouston Gregory Miller Mathew M. Yeh Swan Thung Annette S.H. Gouw Alberto Quaglia Jing Han Ji Huan Cathy Fan James Crawford Yasuni Nakanuma Kenichi Harada Brigitte leBail Claire Castain Nora Frulio Hervé Trillaud Laurent Possenti Jean‐Frédéric Blanc Laurence Chiche Christophe Laurent Charles Balabaud Paulette Bioulac‐Sage Anne Aurélie Raymond Frédéric Saltel |
author_sort |
Margaux Sala |
title |
ASS1 Overexpression: A Hallmark of Sonic Hedgehog Hepatocellular Adenomas; Recommendations for Clinical Practice |
title_short |
ASS1 Overexpression: A Hallmark of Sonic Hedgehog Hepatocellular Adenomas; Recommendations for Clinical Practice |
title_full |
ASS1 Overexpression: A Hallmark of Sonic Hedgehog Hepatocellular Adenomas; Recommendations for Clinical Practice |
title_fullStr |
ASS1 Overexpression: A Hallmark of Sonic Hedgehog Hepatocellular Adenomas; Recommendations for Clinical Practice |
title_full_unstemmed |
ASS1 Overexpression: A Hallmark of Sonic Hedgehog Hepatocellular Adenomas; Recommendations for Clinical Practice |
title_sort |
ass1 overexpression: a hallmark of sonic hedgehog hepatocellular adenomas; recommendations for clinical practice |
publisher |
Wiley |
series |
Hepatology Communications |
issn |
2471-254X |
publishDate |
2020-06-01 |
description |
Until recently, 10% of hepatocellular adenomas (HCAs) remained unclassified (UHCA). Among the UHCAs, the sonic hedgehog HCA (shHCA) was defined by focal deletions that fuse the promoter of Inhibin beta E chain with GLI1. Prostaglandin D2 synthase was proposed as immunomarker. In parallel, our previous work using proteomic analysis showed that most UHCAs constitute a homogeneous subtype associated with overexpression of argininosuccinate synthase (ASS1). To clarify the use of ASS1 in the HCA classification and avoid misinterpretations of the immunohistochemical staining, the aims of this work were to study (1) the link between shHCA and ASS1 overexpression and (2) the clinical relevance of ASS1 overexpression for diagnosis. Molecular, proteomic, and immunohistochemical analyses were performed in UHCA cases of the Bordeaux series. The clinico‐pathological features, including ASS1 immunohistochemical labeling, were analyzed on a large international series of 67 cases. ASS1 overexpression and the shHCA subgroup were superimposed in 15 cases studied by molecular analysis, establishing ASS1 overexpression as a hallmark of shHCA. Moreover, the ASS1 immunomarker was better than prostaglandin D2 synthase and only found positive in 7 of 22 shHCAs. Of the 67 UHCA cases, 58 (85.3%) overexpressed ASS1, four cases were ASS1 negative, and in five cases ASS1 was noncontributory. Proteomic analysis performed in the case of doubtful interpretation of ASS1 overexpression, especially on biopsies, can be a support to interpret such cases. ASS1 overexpression is a specific hallmark of shHCA known to be at high risk of bleeding. Therefore, ASS1 is an additional tool for HCA classification and clinical diagnosis. |
url |
https://doi.org/10.1002/hep4.1514 |
work_keys_str_mv |
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doaj-a964102491fb4c51a8bbff73d7a74e812020-11-25T03:17:19ZengWileyHepatology Communications2471-254X2020-06-014680982410.1002/hep4.1514ASS1 Overexpression: A Hallmark of Sonic Hedgehog Hepatocellular Adenomas; Recommendations for Clinical PracticeMargaux Sala0Delphine Gonzales1Thierry Leste‐Lasserre2Nathalie Dugot‐Senant3Valérie Paradis4Sylvaine Di Tommaso5Jean‐William Dupuy6Vincent Pitard7Cyril Dourthe8Amedeo Sciarra9Christine Sempoux10Linda D. Ferrell11Andrew D. Clouston12Gregory Miller13Mathew M. Yeh14Swan Thung15Annette S.H. Gouw16Alberto Quaglia17Jing Han18Ji Huan19Cathy Fan20James Crawford21Yasuni Nakanuma22Kenichi Harada23Brigitte leBail24Claire Castain25Nora Frulio26Hervé Trillaud27Laurent Possenti28Jean‐Frédéric Blanc29Laurence Chiche30Christophe Laurent31Charles Balabaud32Paulette Bioulac‐Sage33Anne Aurélie Raymond34Frédéric Saltel35BaRITOn Bordeaux Research in Translational Oncology University of Bordeaux INSERM UMR1053 Bordeaux FranceNeurocentre Magendie INSERM U1215 Bordeaux FranceNeurocentre Magendie INSERM U1215 Bordeaux FrancePlateforme d’histopathologie, TBM‐Core US 005 Bordeaux FranceINSERM; APHP, Pathology Department Beaujon Hospital Université de Paris Hopital Beaujon Clichy FranceBaRITOn Bordeaux Research in Translational Oncology University of Bordeaux INSERM UMR1053 Bordeaux FrancePlateforme Protéome Centre de Génomique Fonctionnelle University of Bordeaux Bordeaux FranceImmunoConcept CNRS UMR 5164 University of Bordeaux Bordeaux FranceBaRITOn Bordeaux Research in Translational Oncology University of Bordeaux INSERM UMR1053 Bordeaux FranceService of Clinical Pathology Institute of Pathology Lausanne University Hospital University of Lausanne Lausanne SwitzerlandService of Clinical Pathology Institute of Pathology Lausanne University Hospital University of Lausanne Lausanne SwitzerlandDepartment of Pathology University of California San Francisco CACentre for Liver Disease Research School of Medicine University of Queensland Brisbane QLD AustraliaCentre for Liver Disease Research School of Medicine University of Queensland Brisbane QLD AustraliaUniversity of Washington School of Medicine Seattle WAIcahn School of Medicine at Mount Sinai New York NYDepartment of Pathology University of Groningen University Medical Center Groningen Groningen the NetherlandsDepartment of Cellular Pathology Royal Free London NHS Foundation Trust London United KingdomDepartment of Pathology Zhongshan Hospital Fudan University Shanghai ChinaDepartment of Pathology Zhongshan Hospital Fudan University Shanghai ChinaDepartment of Pathology and Laboratory Medicine Hofstra/Northwell Hempstead NYDepartment of Pathology and Laboratory Medicine Hofstra/Northwell Hempstead NYPathology Division Shizuoka Cancer Center Sunto‐gun JapanDepartment of Human Pathology Kanazawa University Graduate School of Medical Sciences Kanazawa JapanBaRITOn Bordeaux Research in Translational Oncology University of Bordeaux INSERM UMR1053 Bordeaux FranceDepartment of Pathology CHU Bordeaux Bordeaux FranceDepartment of Diagnostic and Interventional Radiology CHU Bordeaux Bordeaux FranceDepartment of Diagnostic and Interventional Radiology CHU Bordeaux Bordeaux FranceDepartment of Hepatology and Oncology INSERM CIC1401 CHU Bordeaux Bordeaux FranceBaRITOn Bordeaux Research in Translational Oncology University of Bordeaux INSERM UMR1053 Bordeaux FranceDepartment of Digestive Surgery CHU Bordeaux Bordeaux FranceDepartment of Digestive Surgery CHU Bordeaux Bordeaux FranceBaRITOn Bordeaux Research in Translational Oncology University of Bordeaux INSERM UMR1053 Bordeaux FranceBaRITOn Bordeaux Research in Translational Oncology University of Bordeaux INSERM UMR1053 Bordeaux FranceBaRITOn Bordeaux Research in Translational Oncology University of Bordeaux INSERM UMR1053 Bordeaux FranceBaRITOn Bordeaux Research in Translational Oncology University of Bordeaux INSERM UMR1053 Bordeaux FranceUntil recently, 10% of hepatocellular adenomas (HCAs) remained unclassified (UHCA). Among the UHCAs, the sonic hedgehog HCA (shHCA) was defined by focal deletions that fuse the promoter of Inhibin beta E chain with GLI1. Prostaglandin D2 synthase was proposed as immunomarker. In parallel, our previous work using proteomic analysis showed that most UHCAs constitute a homogeneous subtype associated with overexpression of argininosuccinate synthase (ASS1). To clarify the use of ASS1 in the HCA classification and avoid misinterpretations of the immunohistochemical staining, the aims of this work were to study (1) the link between shHCA and ASS1 overexpression and (2) the clinical relevance of ASS1 overexpression for diagnosis. Molecular, proteomic, and immunohistochemical analyses were performed in UHCA cases of the Bordeaux series. The clinico‐pathological features, including ASS1 immunohistochemical labeling, were analyzed on a large international series of 67 cases. ASS1 overexpression and the shHCA subgroup were superimposed in 15 cases studied by molecular analysis, establishing ASS1 overexpression as a hallmark of shHCA. Moreover, the ASS1 immunomarker was better than prostaglandin D2 synthase and only found positive in 7 of 22 shHCAs. Of the 67 UHCA cases, 58 (85.3%) overexpressed ASS1, four cases were ASS1 negative, and in five cases ASS1 was noncontributory. Proteomic analysis performed in the case of doubtful interpretation of ASS1 overexpression, especially on biopsies, can be a support to interpret such cases. ASS1 overexpression is a specific hallmark of shHCA known to be at high risk of bleeding. Therefore, ASS1 is an additional tool for HCA classification and clinical diagnosis.https://doi.org/10.1002/hep4.1514 |