Evidence map›Paper›PMID 35676859›Full record

ArticleCancer medicine2023

Characterization of rare histological subtypes of ovarian cancer based on molecular profiling.

Nobutaka Takahashi, Keiichi Hatakeyama, Takeshi Nagashima, Keiichi Ohshima, Kenichi Urakami, Ken Yamaguchi, Yasuyuki Hirashima

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Nobutaka TakahashiDivision of Gynecology, Shizuoka Cancer Center, Sunto-gun, Shizuoka, Japan.ORCID 0000-0002-4194-4388
Keiichi HatakeyamaMedical Genetics Division, Shizuoka Cancer Center Research Institute, Sunto-gun, Shizuoka, Japan.ORCID 0000-0001-6000-5899
Takeshi NagashimaCancer Diagnostics Research Division, Shizuoka Cancer Center Research Institute, Sunto-gun, Shizuoka, Japan.
Keiichi OhshimaMedical Genetics Division, Shizuoka Cancer Center Research Institute, Sunto-gun, Shizuoka, Japan.ORCID 0000-0002-2882-7566
Kenichi UrakamiCancer Diagnostics Research Division, Shizuoka Cancer Center Research Institute, Sunto-gun, Shizuoka, Japan.
Ken YamaguchiShizuoka Cancer Center, Sunto-gun, Shizuoka, Japan.
Yasuyuki HirashimaDivision of Gynecology, Shizuoka Cancer Center, Sunto-gun, Shizuoka, Japan.
Shizuoka Cancer Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivePan-cancer analysis across The Cancer Genome Atlas has revealed the molecular profiles of major types of carcinomas. High-grade serous carcinomas (HGSCs) have been characterized; however, in ovarian cancer, the profile of carcinoma with minor histopathological changes remains unclear. This study aimed to perform the molecular profiling of rare malignant ovarian tumors, including non-epithelial tumors (NETs; germ cell tumors and sex cord tumors) and clear cell carcinoma (CCC), to determine how they differ from the major HGSCs.

methodsSixty-nine malignant ovarian tumors surgically resected at the Shizuoka Cancer Center between January 2014 and March 2019 were classified based on their histopathological types. The germline and somatic mutations in these carcinomas, including NETs, were determined using next-generation sequencing. Gene expression analysis was performed to investigate the major pathways of drug resistance, which is a characteristic of CCC.

resultsNETs harbored copy-neutral loss of heterozygosity, accompanied by a high homologous recombination deficiency score; germline mutations of PALB2 and BARD1 were identified in two patients with NET. In chemoresistant CCC, the epithelial-mesenchymal transition pathway was activated regardless of ABC transporter expression.

conclusionThis study revealed some genomic characteristics of rare malignant ovarian tumors, including NETs and CCC.

Indexed as

CarcinomaOvarian NeoplasmsBRCA1 ProteinFemaleGerm-Line MutationHumansBRCA1 Proteinclear cell carcinomamolecular profilingnon-epithelial tumorovarian tumor

Identifiers

PMID35676859
PMCPMC9844652
OpenAlexW4282030249

What OpenQuestion holds

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LicenceCC BY
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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.