Evidence map›Paper›PMID 29736797›Full record

ArticleVirchows Archiv : an international journal of pathology2018

β-catenin (CTNNB1) mutation and LEF1 expression in sinonasal glomangiopericytoma (sinonasal-type hemangiopericytoma).

Yuka Suzuki, Shu Ichihara, Tomonori Kawasaki, Hiroyuki Yanai, Satoshi Kitagawa, Yoshie Shimoyama, Shigeo Nakamura, Masato Nakaguro

Abstract read
PubMed Publisher
In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

11 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Article
  3. Utility of LEF1 to differentiate desmoid fibromatosis from its histologic mimics.Virchows Archiv : an international journal of pathology · 2024
    Article
  4. Review
  5. Review
  6. Glomangiopericytoma withBMJ case reports · 2023
    Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. 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

8 authors at 4 institutions in 1 country.

Yuka SuzukiDepartment of Pathology and Clinical Laboratories, Nagoya University Hospital, 65 Tsurumai-cho, Showa-ku, Nagoya, 466-8560, Japan.
Shu IchiharaDepartment of Pathology, Nagoya Medical Center, Nagoya, Japan.
Tomonori KawasakiDepartment of Pathology, Nagoya Medical Center, Nagoya, Japan.
Hiroyuki YanaiDepartment of Pathology, Okayama University Hospital, Okayama, Japan.
Satoshi KitagawaDepartment of Pathology, Toyota Memorial Hospital, Toyota, Japan.
Yoshie ShimoyamaDepartment of Pathology and Clinical Laboratories, Nagoya University Hospital, 65 Tsurumai-cho, Showa-ku, Nagoya, 466-8560, Japan.
Shigeo NakamuraDepartment of Pathology and Clinical Laboratories, Nagoya University Hospital, 65 Tsurumai-cho, Showa-ku, Nagoya, 466-8560, Japan.
Masato NakaguroDepartment of Pathology and Clinical Laboratories, Nagoya University Hospital, 65 Tsurumai-cho, Showa-ku, Nagoya, 466-8560, Japan. mnakaguro@med.nagoya-u.ac.jp.ORCID http://orcid.org/0000-0001-6987-3043
Nagoya University Hospital · JPNagoya Medical Center · JPOkayama University Hospital · JPToyota Memorial Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sinonasal glomangiopericytoma (SN-GPC) is an uncommon mesenchymal tumor with myoid differentiation. Recently, mutations in exon 3 of the gene coding for β-catenin (CTNNB1) and its nuclear expression were discovered in SN-GPC. β-catenin protein is a key regulatory molecule of the canonical Wnt signaling pathway. The expression of β-catenin target proteins is not well characterized in SN-GPC. We examined three SN-GPCs by immunohistochemistry and CTNNB1 mutation analysis. All cases expressed nuclear β-catenin. We identified CTNNB1 exon 3 mutations in two analyzable cases. Lymphoid enhancer-binding factor 1 (LEF1), a protein downstream from β-catenin, was also expressed in all cases. Our results further characterized the activation of the Wnt signaling pathway caused by CTNNB1 exon 3 mutation and suggest the utility of LEF1 immunohistochemistry in the differential diagnosis of SN-GPC.

Indexed as

Biomarkers, TumorMutationAged, 80 and overbeta CateninDiagnosis, DifferentialDNA Mutational AnalysisFemaleGlomus TumorHemangiopericytomaHumansImmunohistochemistryLymphoid Enhancer-Binding Factor 1MaleMiddle AgedNose NeoplasmsPredictive Value of Testsbeta CateninBiomarkers, TumorCTNNB1 protein, humanLEF1 protein, humanLymphoid Enhancer-Binding Factor 1CTNNB1LEF1Sinonasal glomangiopericytomaβ-catenin

Identifiers

PMID29736797
OpenAlexW2801508105

What OpenQuestion holds

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Registered trials

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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.