Evidence map›Paper›PMID 39807103›Full record

ArticleOncology letters2025

Analysis of endometrial liquid‑based cytology samples to detect somatic mutations and classify ovarian cancer.

Michiko Kubo-Kaneda, Eiji Kondo, Ryo Nimura, Kota Okamoto, Tsuyoshi Matsumoto, Kenta Yoshida, Makoto Ikejiri, Maki Nakamura, Hiroshi Imai, Yoshinaga Okugawa and 2 more

Abstract read
In one paragraph

Article in Oncology letters, 2025. 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
–field-weighted citation impact
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.

  1. Review
  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.

Michiko Kubo-KanedaDepartment of Obstetrics and Gynecology, Mie University School of Medicine, Tsu, Mie 514-8507, Japan.
Eiji KondoDepartment of Obstetrics and Gynecology, Mie University School of Medicine, Tsu, Mie 514-8507, Japan.
Ryo NimuraDepartment of Gynecologic Oncology, Cancer Institute Hospital, Tokyo 135-8550, Japan.
Kota OkamotoDepartment of Obstetrics and Gynecology, Mie University School of Medicine, Tsu, Mie 514-8507, Japan.
Tsuyoshi MatsumotoDepartment of Obstetrics and Gynecology, Mie University School of Medicine, Tsu, Mie 514-8507, Japan.
Kenta YoshidaDepartment of Obstetrics and Gynecology, Mie University School of Medicine, Tsu, Mie 514-8507, Japan.
Makoto IkejiriDepartment of Genomic Medicine, Mie University School of Medicine, Tsu, Mie 514-8507, Japan.
Maki NakamuraDepartment of Genomic Medicine, Mie University School of Medicine, Tsu, Mie 514-8507, Japan.
Hiroshi ImaiDepartment of Oncologic Pathology, Mie University School of Medicine, Tsu, Mie 514-8507, Japan.
Yoshinaga OkugawaDepartment of Genomic Medicine, Mie University School of Medicine, Tsu, Mie 514-8507, Japan.
Kaname NakataniDepartment of Genomic Medicine, Mie University School of Medicine, Tsu, Mie 514-8507, Japan.
Tomoaki IkedaDepartment of Obstetrics and Gynecology, Mie University School of Medicine, Tsu, Mie 514-8507, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ovarian cancer has a poor prognosis, and screening methods have not been established. Biomarkers based on molecular genetic characteristics must be identified to develop diagnostic and therapeutic strategies for all cancer types, particularly ovarian cancer. The present study aimed to evaluate the usefulness of genetic analysis of cervical and endometrial liquid-based cytology (LBC) specimens for detecting somatic mutations in patients with ovarian cancer. The data of 19 patients with ovarian cancer treated between August 2019 and July 2022 were analyzed. LBC specimens from the cervix and endometrium of patients with preoperatively suspected ovarian cancer were collected, and genomic DNA was extracted from these LBC specimens and surgically removed cancer tissue sections for genetic analysis. Next-generation sequencing (NGS) analysis of cervical and endometrial LBC revealed genetic mutations similar to those in formalin-fixed, paraffin-embedded (FFPE) tissues in 42% of ovarian cancer cases, including negative cervical and endometrial cytology cases and early-stage cases. The pathogenic variants detected were

Indexed as

cytologymutationnext-generation sequencingovarian cancer

Identifiers

PMID39807103
PMCPMC11726286

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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.