Evidence map›Paper›PMID 32490318›Full record

ArticleHepatology communications2020

ASS1 Overexpression: A Hallmark of Sonic Hedgehog Hepatocellular Adenomas; Recommendations for Clinical Practice.

Margaux Sala, Delphine Gonzales, Thierry Leste-Lasserre, Nathalie Dugot-Senant, Valérie Paradis, Sylvaine Di Tommaso, Jean-William Dupuy, Vincent Pitard, Cyril Dourthe, Amedeo Sciarra and 26 more

Open access · goldAbstract read
In one paragraph

Article in Hepatology communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.6field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Molecular diagnostics of hepatobiliary and pancreatic neoplasias.Virchows Archiv : an international journal of pathology · 2024
    Review
  9. The Liver and Glycogen: In Sickness and in Health.International journal of molecular sciences · 2023
    Review
  10. Review
  11. Hepatocellular adenoma: Where are we now?World journal of gastroenterology · 2022
    Article
  12. Article
  13. Hepatocellular adenoma in men: A nationwide assessment of pathology and correlation with clinical course.Liver international : official journal of the International Association for the Study of the Liver · 2021
    Article
  14. Article
  15. Hepatocellular adenomas: recent updates.Journal of pathology and translational medicine · 2021
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

36 authors at 15 institutions in 8 countries.

Margaux SalaBaRITOn Bordeaux Research in Translational Oncology University of Bordeaux INSERM UMR1053 Bordeaux France.ORCID https://orcid.org/0000-0003-3483-361X
Delphine GonzalesNeurocentre Magendie INSERM U1215 Bordeaux France.ORCID https://orcid.org/0000-0002-6307-4280
Thierry Leste-LasserreNeurocentre Magendie INSERM U1215 Bordeaux France.ORCID https://orcid.org/0000-0001-8328-3816
Nathalie Dugot-SenantPlateforme d'histopathologie, TBM-Core US 005 Bordeaux France.
Valérie ParadisINSERM; APHP, Pathology Department Beaujon Hospital Université de Paris Hopital Beaujon Clichy France.ORCID https://orcid.org/0000-0003-3142-3762
Sylvaine Di TommasoBaRITOn Bordeaux Research in Translational Oncology University of Bordeaux INSERM UMR1053 Bordeaux France.ORCID https://orcid.org/0000-0003-4507-2844
Jean-William DupuyPlateforme Protéome Centre de Génomique Fonctionnelle University of Bordeaux Bordeaux France.ORCID https://orcid.org/0000-0002-2448-4797
Vincent PitardImmunoConcept CNRS UMR 5164 University of Bordeaux Bordeaux France.ORCID https://orcid.org/0000-0001-6380-2308
Cyril DourtheBaRITOn Bordeaux Research in Translational Oncology University of Bordeaux INSERM UMR1053 Bordeaux France.ORCID https://orcid.org/0000-0002-0941-1303
Amedeo SciarraService of Clinical Pathology Institute of Pathology Lausanne University Hospital University of Lausanne Lausanne Switzerland.ORCID https://orcid.org/0000-0002-7550-0312
Christine SempouxService of Clinical Pathology Institute of Pathology Lausanne University Hospital University of Lausanne Lausanne Switzerland.
Linda D FerrellDepartment of Pathology University of California San Francisco CA.
Andrew D CloustonCentre for Liver Disease Research School of Medicine University of Queensland Brisbane QLD Australia.
Gregory MillerCentre for Liver Disease Research School of Medicine University of Queensland Brisbane QLD Australia.
Mathew M YehUniversity of Washington School of Medicine Seattle WA.
Swan ThungIcahn School of Medicine at Mount Sinai New York NY.
Annette S H GouwDepartment of Pathology University of Groningen University Medical Center Groningen Groningen the Netherlands.
Alberto QuagliaDepartment of Cellular Pathology Royal Free London NHS Foundation Trust London United Kingdom.
Jing HanDepartment of Pathology Zhongshan Hospital Fudan University Shanghai China.
Ji HuanDepartment of Pathology Zhongshan Hospital Fudan University Shanghai China.
Cathy FanDepartment of Pathology and Laboratory Medicine Hofstra/Northwell Hempstead NY.
James CrawfordDepartment of Pathology and Laboratory Medicine Hofstra/Northwell Hempstead NY.
Yasuni NakanumaPathology Division Shizuoka Cancer Center Sunto-gun Japan.
Kenichi HaradaDepartment of Human Pathology Kanazawa University Graduate School of Medical Sciences Kanazawa Japan.
Brigitte le BailBaRITOn Bordeaux Research in Translational Oncology University of Bordeaux INSERM UMR1053 Bordeaux France.ORCID https://orcid.org/0000-0002-2607-1734
Claire CastainDepartment of Pathology CHU Bordeaux Bordeaux France.ORCID https://orcid.org/0000-0001-8474-4805
Nora FrulioDepartment of Diagnostic and Interventional Radiology CHU Bordeaux Bordeaux France.ORCID https://orcid.org/0000-0003-1374-7624
Hervé TrillaudDepartment of Diagnostic and Interventional Radiology CHU Bordeaux Bordeaux France.ORCID https://orcid.org/0000-0001-8607-6716
Laurent PossentiDepartment of Hepatology and Oncology INSERM CIC1401 CHU Bordeaux Bordeaux France.
Jean-Frédéric BlancBaRITOn Bordeaux Research in Translational Oncology University of Bordeaux INSERM UMR1053 Bordeaux France.ORCID https://orcid.org/0000-0001-6172-9485
Laurence ChicheDepartment of Digestive Surgery CHU Bordeaux Bordeaux France.ORCID https://orcid.org/0000-0002-7580-2476
Christophe LaurentDepartment of Digestive Surgery CHU Bordeaux Bordeaux France.
Charles BalabaudBaRITOn Bordeaux Research in Translational Oncology University of Bordeaux INSERM UMR1053 Bordeaux France.ORCID https://orcid.org/0000-0003-0081-8112
Paulette Bioulac-SageBaRITOn Bordeaux Research in Translational Oncology University of Bordeaux INSERM UMR1053 Bordeaux France.ORCID https://orcid.org/0000-0001-5952-0623
Anne Aurélie RaymondBaRITOn Bordeaux Research in Translational Oncology University of Bordeaux INSERM UMR1053 Bordeaux France.ORCID https://orcid.org/0000-0003-2697-9352
Frédéric SaltelBaRITOn Bordeaux Research in Translational Oncology University of Bordeaux INSERM UMR1053 Bordeaux France.ORCID https://orcid.org/0000-0002-0724-9680
Université de Bordeaux · FRCentre Hospitalier Universitaire de Bordeaux · FRInserm · FRHofstra University · USSun Yat-sen University · CNThe University of Queensland · AUUniversity of Lausanne · CHCentre National de la Recherche Scientifique · FRIcahn School of Medicine at Mount Sinai · USKanazawa University · JPRoyal Free London NHS Foundation Trust · GBShizuoka Cancer Center · JPUniversity Medical Center Groningen · NLUniversity of California, San Francisco · USUniversity of Washington · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Identifiers

PMID32490318
PMCPMC7262286
OpenAlexW3015521066

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.