Evidence map›Paper›PMID 36013219›Full record

ArticleJournal of personalized medicine2022

Wnt/β-Catenin-Pathway Alterations and Homologous Recombination Deficiency in Cholangiocarcinoma Cell Lines and Clinical Samples: Towards Specific Vulnerabilities.

Alexander Scheiter, Frederik Hierl, Ingrid Winkel, Felix Keil, Margit Klier-Richter, Cédric Coulouarn, Florian Lüke, Arne Kandulski, Matthias Evert, Wolfgang Dietmaier and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of personalized medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. 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 3 institutions in 2 countries.

Alexander ScheiterInstitute of Pathology, University of Regensburg, 93053 Regensburg, Germany.ORCID 0000-0001-6734-261X
Frederik HierlInstitute of Pathology, University of Regensburg, 93053 Regensburg, Germany.
Ingrid WinkelInstitute of Pathology, University of Regensburg, 93053 Regensburg, Germany.
Felix KeilInstitute of Pathology, University of Regensburg, 93053 Regensburg, Germany.ORCID 0000-0002-0651-5916
Margit Klier-RichterInstitute of Pathology, University of Regensburg, 93053 Regensburg, Germany.
Cédric CoulouarnINSERM, Université de Rennes, F-35042 Rennes, France.
Florian LükeBavarian Center for Cancer Research/BZKF, 91054 Bavaria, Germany.
Arne KandulskiDepartment of Internal Medicine I, University Hospital Regensburg, 93053 Regensburg, Germany.
Matthias EvertInstitute of Pathology, University of Regensburg, 93053 Regensburg, Germany.
Wolfgang DietmaierInstitute of Pathology, University of Regensburg, 93053 Regensburg, Germany.
Diego F CalvisiInstitute of Pathology, University of Regensburg, 93053 Regensburg, Germany.
Kirsten UtpatelInstitute of Pathology, University of Regensburg, 93053 Regensburg, Germany.
University of Regensburg · DEUniversity Hospital Regensburg · DEInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cholangiocarcinoma (CCA) features a dismal prognosis with limited treatment options. Genomic studies have unveiled several promising targets in this disease, including fibroblast growth factor receptor (FGFR) fusions and isocitrate dehydrogenase (IDH) mutations. To fully harness the potential of genomically informed therapies in CCA, it is necessary to thoroughly characterize the available model organisms, including cell lines. One parameter to investigate in CCA is homologous recombination deficiency (HRD). While mutations in homologous recombinational repair (HRR)-related genes have been detected, their predictive value remains undetermined. Using a targeted next-generation sequencing approach, we analyzed 12 human CCA cell lines and compared them to 62 CCA samples of the molecular tumor board cohort. The AmoyDx

Indexed as

APCcholangiocarcinomaHRDintraductal papillary neoplasm of the bile ductOlaparibPARPWNTβ-catenin

Identifiers

PMID36013219
PMCPMC9410222
OpenAlexW4289344412

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.