Evidence map›Paper›PMID 42482410›Full record

ArticlePathology international2026

Prevalence and Independence of p53 Signatures and β-Catenin Signatures in Risk-Reducing Salpingo-Oophorectomy Specimens.

Kei Koyama, Hikaru Tsukita, Takahiro Ishinari, Ayana Takahashi, Ken Miyabe, Makoto Yoshida, Yukitsugu Kudo-Asabe, Hiroshi Nanjo, Masato Waga, Enami Kaneko and 5 more

Abstract read
In one paragraph

Article in Pathology international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Kei KoyamaDepartment of Quantitative Pathology, Graduate School of Medicine, Akita University, Akita, Akita, Japan.ORCID https://orcid.org/0009-0004-1859-094X
Hikaru TsukitaDepartment of Quantitative Pathology, Graduate School of Medicine, Akita University, Akita, Akita, Japan.
Takahiro IshinariDepartment of Quantitative Pathology, Graduate School of Medicine, Akita University, Akita, Akita, Japan.
Ayana TakahashiDepartment of Quantitative Pathology, Graduate School of Medicine, Akita University, Akita, Akita, Japan.
Ken MiyabeDepartment of Quantitative Pathology, Graduate School of Medicine, Akita University, Akita, Akita, Japan.
Makoto YoshidaDepartment of Quantitative Pathology, Graduate School of Medicine, Akita University, Akita, Akita, Japan.
Yukitsugu Kudo-AsabeDepartment of Quantitative Pathology, Graduate School of Medicine, Akita University, Akita, Akita, Japan.
Hiroshi NanjoDepartment of Pathology, Akita University Hospital, Akita, Akita, Japan.
Masato WagaDepartment of Obstetrics and Gynecology, Graduate School of Medicine, Akita University, Akita, Akita, Japan.
Enami KanekoDepartment of Obstetrics and Gynecology, Graduate School of Medicine, Akita University, Akita, Akita, Japan.
Takeo HirakawaDepartment of Obstetrics and Gynecology, Graduate School of Medicine, Akita University, Akita, Akita, Japan.
Tae SugawaraDepartment of Obstetrics and Gynecology, Graduate School of Medicine, Akita University, Akita, Akita, Japan.
Kenichi MakinoDepartment of Obstetrics and Gynecology, Graduate School of Medicine, Akita University, Akita, Akita, Japan.
Yukihiro TeradaDepartment of Obstetrics and Gynecology, Graduate School of Medicine, Akita University, Akita, Akita, Japan.
Akiteru GotoDepartment of Quantitative Pathology, Graduate School of Medicine, Akita University, Akita, Akita, Japan.ORCID https://orcid.org/0000-0001-8776-9004

Funding

Japan Society for the Promotion of Science JP 25K18737
6 · The paper itself

Abstract

Clusters of epithelial cells of the fallopian tube exhibiting aberrant p53 expression, termed "p53 signatures," are detected at a relatively high frequency and have been regarded as putative precursors of high-grade serous carcinoma (HGSC). In contrast, the recently proposed "β-catenin signature" represents a distinct tubal epithelial alteration characterized by the aberrant expression of β-catenin, the biological significance of which remains unclear. To clarify the frequency and spatial relationship between the two lesions, we analyzed 30 consecutive risk-reducing salpingo-oophorectomy specimens from BRCA1/2 mutation carriers using the sectioning and extensively examining the fimbriated end protocol and performed immunohistochemical evaluation for p53, β-catenin, and Ki-67. p53 signatures and β-catenin signatures were each identified in seven cases (23%). Two cases (6.7%) harbored both lesions; however, no spatial overlap or histological continuity was observed. Neither lesion demonstrated significant associations with BRCA mutation subtype, age, body mass index, or parity. Furthermore, no cases showed serous tubal intraepithelial lesion, serous tubal intraepithelial carcinoma, or HGSC. These findings suggest that p53 signatures and β-catenin signatures may represent distinct localized epithelial alterations in the fallopian tube, although further molecular and spatial analyses are required to clarify their biological relationship.

Indexed as

beta CateninFallopian Tube NeoplasmsOvarian NeoplasmsTumor Suppressor Protein p53AdultBiomarkers, TumorBRCA1 ProteinBRCA2 ProteinCystadenocarcinoma, SerousFallopian TubesFemaleHumansImmunohistochemistryMiddle AgedMutationPrevalencebeta CateninBiomarkers, TumorBRCA1 ProteinBRCA2 ProteinCTNNB1 protein, humanTP53 protein, humanTumor Suppressor Protein p53BRCA mutationfallopian tubep53β‐catenin

Identifiers

PMID42482410
PMCPMC13389328

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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.