Evidence map›Paper›PMID 30787326›Full record

ArticleScientific reports2019

Clinicopathological correlation of ARID1A status with HDAC6 and its related factors in ovarian clear cell carcinoma.

Mitsutake Yano, Tomomi Katoh, Mariko Miyazawa, Masaki Miyazawa, Naoki Ogane, Maiko Miwa, Kosei Hasegawa, Hisashi Narahara, Masanori Yasuda

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

19 citing papers in PubMed, 37 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

9 authors at 4 institutions in 1 country.

Mitsutake YanoDepartment of Pathology, Saitama Medical University International Medical Centre, Saitama, Japan. yano1210@oita-u.ac.jp.
Tomomi KatohDepartment of Pathology, Saitama Medical University International Medical Centre, Saitama, Japan.
Mariko MiyazawaDepartment of Obstetrics and Gynaecology, Tokai University School of Medicine, Kanagawa, Japan.
Masaki MiyazawaDepartment of Obstetrics and Gynaecology, Tokai University School of Medicine, Kanagawa, Japan.
Naoki OganeDivision of Pathology, Ashigarakami Hospital, Kanagawa, Japan.
Maiko MiwaDepartment of Gynaecologic Oncology, Saitama Medical University International Medical Centre, Saitama, Japan.
Kosei HasegawaDepartment of Gynaecologic Oncology, Saitama Medical University International Medical Centre, Saitama, Japan.ORCID 0000-0002-1903-7001
Hisashi NaraharaDepartments of Obstetrics and Gynaecology, Oita University Faculty of Medicine, Oita, Japan.
Masanori YasudaDepartment of Pathology, Saitama Medical University International Medical Centre, Saitama, Japan. m_yasuda@saitama-med.ac.jp.
Saitama Medical University · JPOita University · JPTokai University · JPSaitama International Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ovarian clear cell carcinoma (OCCC) is associated with a frequent loss in ARID1A function. ARID1A reportedly suppresses histone deacetylase (HDAC)6 in OCCC directly. Here, we evaluated the clinical significance of HDAC6 expression and its related factors in terms of ARID1A status. Immunohistochemical expression of HDAC6, hypoxia inducible factors-1α (HIF-1α), programmed death-1 ligand (PD-L1), CD44 (cancer stem cell marker), and ARID1A was analysed for 106 OCCC patients. High nuclear HDAC6 expression correlated with patient death (p = 0.038). In the multivariate analysis of overall survival, surgical status (complete or incomplete resection) (hazard ratio (HR) = 17.5; p = <0.001), HDAC6 nuclear expression (HR = 1.68; p = 0.034), and PD-L1 expression (HR = 1.95; p = 0.022) were the independent prognostic factors. HDAC6 upregulation and ARID1A loss did not necessarily occur simultaneously. High HDAC6 expression was associated with poor prognosis in OCCC with ARID1A loss; this was not observed without ARID1A loss. HDAC6 expression showed a significant positive correlation with HIF-1α, PD-L1, and CD44. In OCCC, HDAC6 involvement in prognosis depended on ARID1A status. HDAC6 also led to immuno- and hypoxia- tolerance and cancer stem cell phenotype. HDAC6 is a promising therapeutic target for OCCC with loss of ARID1A.

Indexed as

AdultAgedB7-H1 AntigenCarcinomaCell NucleusDisease-Free SurvivalDNA-Binding ProteinsEpitheliumFemaleGene Expression Regulation, NeoplasticHistone Deacetylase 6HumansKaplan-Meier EstimateMiddle AgedOvarian NeoplasmsOvaryARID1A protein, humanB7-H1 AntigenCD274 protein, humanDNA-Binding ProteinsHDAC6 protein, humanHistone Deacetylase 6Transcription Factors

Identifiers

PMID30787326
PMCPMC6382831
OpenAlexW2916880279

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.