Evidence map›Paper›PMID 31897818›Full record

ArticleVirchows Archiv : an international journal of pathology2020

Histotype-specific analysis of acid ceramidase expression in ovarian cancer.

Ahmed El-Balat, Thomas Karn, Uwe Holtrich, Sven Becker, Stefan Kommoss, Balázs Győrffy, Michael S Anglesio, David G Huntsman, Zacharias Drosos, Achim Rody and 2 more

Abstract read
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In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
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

12 authors at 6 institutions in 3 countries.

Ahmed El-BalatGoethe University Frankfurt, Department of Obstetrics and Gynecology, Frankfurt, Germany. ahmed.el-balat@kgu.de.ORCID https://orcid.org/0000-0002-0560-8395
Thomas KarnGoethe University Frankfurt, Department of Obstetrics and Gynecology, Frankfurt, Germany.
Uwe HoltrichGoethe University Frankfurt, Department of Obstetrics and Gynecology, Frankfurt, Germany.
Sven BeckerGoethe University Frankfurt, Department of Obstetrics and Gynecology, Frankfurt, Germany.
Stefan KommossDepartment of Woman's Health, Tuebingen University Hospital, Tuebingen, Germany.
Balázs GyőrffyMTA TTK Lendület Cancer Biomarker Research Group & Semmelweis, University Second Department of Pediatrics, Budapest, Hungary.
Michael S AnglesioDepartment of Obstetrics and Gynecology, University of British Columbia, Vancouver, Canada.
David G HuntsmanDepartment of Obstetrics and Gynecology, University of British Columbia, Vancouver, Canada.
Zacharias DrososGynecology and Obstetrics, University Hospital Lübeck, Lübeck, Germany.
Achim RodyGynecology and Obstetrics, University Hospital Lübeck, Lübeck, Germany.
Heidrun GevenslebenInstitute of Pathology, University Hospital Bonn, Bonn, Germany.
Lars C HankerGynecology and Obstetrics, University Hospital Lübeck, Lübeck, Germany.
Goethe University Frankfurt · DEUniversity of Lübeck · DEUniversity of British Columbia · CASemmelweis University · HUUniversity Hospital Bonn · DEUniversity of Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acid ceramidase (ASAH1) is a key player in sphingolipid metabolism and signaling. It has prognostic value for several cancers, but histotype-specific analyses of ovarian cancer are not yet available. We used three retrospective TMA cohorts encompassing a total of 1106 ovarian cancers with follow-up data for immunohistochemical analysis of acid ceramidase (ASAH1) expression. Patients with sub-optimal debulking and persistent residual tumor after surgery introduced bias in the prognostic analysis and were excluded from further studies. Overall, we detected an association of ASAH1 expression with better prognosis in ovarian cancer patients. ASAH1 expression differed between histological ovarian cancer histotypes with most frequent expression in endometrioid and clear cell ovarian cancer, which are both associated with good prognosis. Stratified subgroup analyses within these histotypes did not reveal significant survival differences, but the power of the analysis may be limited by smaller sample sizes. In contrast to breast cancer, we found only a modest concordance between estrogen receptor status and ASAH1 expression within the endometrioid ovarian cancer histotype. In an exploratory analysis of estrogen receptor negative endometrioid ovarian cancer, ASAH1 expression was associated with significantly better overall survival (P = 0.007). Acid ceramidase is most frequently expressed in endometrioid and clear cell histotypes and could add independent prognostic value to estrogen receptor in endometrioid ovarian cancer. Modulating sphingolipid metabolism may lead to novel therapeutic intervention strategies for this disease.

Indexed as

Acid CeramidaseBiomarkers, TumorCarcinoma, EndometrioidCohort StudiesFemaleFollow-Up StudiesHumansMiddle AgedOvarian NeoplasmsOvaryPrognosisAcid CeramidaseASAH1 protein, humanBiomarkers, TumorOvarian cancer histotypesPrognosisSphingolipid signaling

Identifiers

PMID31897818
OpenAlexW2996854366

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.