Evidence map›Paper›PMID 26572704›Full record

ReviewOncology reports2016

ARID1A gene mutation in ovarian and endometrial cancers (Review).

Takashi Takeda, Kouji Banno, Ryuichiro Okawa, Megumi Yanokura, Moito Iijima, Haruko Irie-Kunitomi, Kanako Nakamura, Miho Iida, Masataka Adachi, Kiyoko Umene and 5 more

Open access · hybridAbstract readReview
In one paragraph

Review in Oncology reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 106 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
106citing papers in PubMed, 1 pooled it
5.9field-weighted citation impact, top 3% 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

106 citing papers in PubMed, 1 synthesis or guideline pooled it, 189 citations in OpenAlex.

  1. Pooled it
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  7. Review
  8. Article
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  11. Review
  12. Review
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  15. Review
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  17. Article
  18. Article
  19. ARID1A and Its Impact Across the Hallmarks of Cancer.International journal of molecular sciences · 2025
    Review
  20. Article

46 more citing papers are in PubMed but not listed here.

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 at 1 institution in 1 country.

Takashi TakedaDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo 160‑8582, Japan.
Kouji BannoDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo 160‑8582, Japan.
Ryuichiro OkawaDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo 160‑8582, Japan.
Megumi YanokuraDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo 160‑8582, Japan.
Moito IijimaDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo 160‑8582, Japan.
Haruko Irie-KunitomiDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo 160‑8582, Japan.
Kanako NakamuraDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo 160‑8582, Japan.
Miho IidaDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo 160‑8582, Japan.
Masataka AdachiDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo 160‑8582, Japan.
Kiyoko UmeneDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo 160‑8582, Japan.
Yuya NogamiDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo 160‑8582, Japan.
Kenta MasudaDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo 160‑8582, Japan.
Yusuke KobayashiDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo 160‑8582, Japan.
Eiichiro TominagaDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo 160‑8582, Japan.
Daisuke AokiDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo 160‑8582, Japan.
Keio University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The AT-rich interacting domain‑containing protein 1A gene (ARID1A) encodes ARID1A, a member of the SWI/SNF chromatin remodeling complex. Mutation of ARID1A induces changes in expression of multiple genes (CDKN1A, SMAD3, MLH1 and PIK3IP1) via chromatin remodeling dysfunction, contributes to carcinogenesis, and has been shown to cause transformation of cells in association with the PI3K/AKT pathway. Information on ARID1A has emerged from comprehensive genome‑wide analyses with next‑generation sequencers. ARID1A mutations have been found in various types of cancer and occur at high frequency in endometriosis‑associated ovarian cancer, including clear cell adenocarcinoma and endometrioid adenocarcinoma, and also occur at endometrial cancer especially in endometrioid adenocarcinoma. It has also been suggested that ARID1A mutation occurs at the early stage of canceration from endometriosis to endometriosis‑associated carcinoma in ovarian cancer and also from atypical endometrial hyperplasia to endometrioid adenocarcinoma in endometrial cancer. Therefore, development of a screening method that can detect mutations of ARID1A and activation of the PI3K/AKT pathway might enable early diagnosis of endometriosis‑associated ovarian cancers and endometrial cancers. Important results may also emerge from a current clinical trial examining a multidrug regimen of temsirolimus, a small molecule inhibitor of the PI3K/AKT pathway, for treatment of advanced ovarian clear cell adenocarcinoma with ARID1A mutation and PI3K/AKT pathway activation. Also administration of sorafenib, a multikinase inhibitor, can inhibit cancer proliferation with PIK3CA mutation and resistance to mTOR inhibitors and GSK126, a molecular‑targeted drug can inhibit proliferation of ARID1A‑mutated ovarian clear cell adenocarcinoma cells by targeting and inhibiting EZH2. Further studies are needed to determine the mechanism of chromatin remodeling dysregulation initiated by ARID1A mutation, to develop methods for early diagnosis, to investigate new cancer therapy targeting ARID1A, and to examine the involvement of ARID1A mutations in development, survival and progression of cancer cells.

Indexed as

MutationDNA-Binding ProteinsEndometrial NeoplasmsFemaleHumansNuclear ProteinsOvarian NeoplasmsTranscription FactorsARID1A protein, humanDNA-Binding ProteinsNuclear ProteinsTranscription Factors

Identifiers

PMID26572704
PMCPMC4689482
OpenAlexW2174510671

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.