Evidence map›Paper›PMID 36681835›Full record

ArticleJournal of translational medicine2023

The epigenetic factor CHD4 contributes to metastasis by regulating the EZH2/β-catenin axis and acts as a therapeutic target in ovarian cancer.

Jieyu Wang, Fangfang Zhong, Jun Li, Huiran Yue, Wenzhi Li, Xin Lu

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 14 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

6 authors at 2 institutions in 1 country.

Jieyu WangDepartment of Gynecology, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, 200090, China.
Fangfang ZhongDepartment of Pathology, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, 200090, China.
Jun LiDepartment of Gynecology, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, 200090, China.
Huiran YueDepartment of Gynecology, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, 200090, China.
Wenzhi LiDepartment of Gynecology, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, 200090, China.
Xin LuDepartment of Gynecology, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, 200090, China. xinludoc@126.com.ORCID 0000-0003-1639-9549
Fudan University · CNObstetrics and Gynecology Hospital of Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe overall survival rate of patients with advanced ovarian cancer (OC) has remained static for several decades. Advanced ovarian cancer is known for its poor prognosis due to extensive metastasis. Epigenetic alterations contribute to tumour progression and therefore are of interest for potential therapeutic strategies.

methodsFollowing our previous study, we identified that CHD4, a chromatin remodelling factor, plays a strong role in ovarian cancer cell metastasis. We investigated the clinical significance of CHD4 through TCGA and GEO database analyses and explored the effect of CHD4 expression modulation and romidepsin treatment on the biological behaviour of ovarian cancer through CCK-8 and transwell assays. Bioluminescence imaging of tumours in xenografted mice was applied to determine the therapeutic effect of romidepsin. GSEA and western blotting were used to screen the regulatory mechanism of CHD4.

resultsIn ovarian cancer patient specimens, high CHD4 expression was associated with a poor prognosis. Loss of function of CHD4 in ovarian cancer cells induced suppression of migration and invasion. Mechanistically, CHD4 knockdown suppressed the expression of EZH2 and the nuclear accumulation of β-catenin. CHD4 also suppressed the metastasis of ovarian cancer cells and prevented disease progression in a mouse model. To inhibit the functions of CHD4 that are mediated by histone deacetylase, we evaluated the effect of the HDAC1/2 selective inhibitor romidepsin. Our findings indicated that treatment with romidepsin suppressed the progression of metastases in vitro and in vivo.

conclusionsCollectively, our results uncovered an oncogenic function of CHD4 in ovarian cancer and provide a rationale for clinical trials of romidepsin in ovarian cancer patients.

Indexed as

Mi-2 Nucleosome Remodeling and Deacetylase ComplexOvarian NeoplasmsAnimalsbeta CateninCell Line, TumorEnhancer of Zeste Homolog 2 ProteinEpigenesis, GeneticFemaleHumansMicebeta CateninCHD4 protein, humanEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanMi-2 Nucleosome Remodeling and Deacetylase ComplexChromodomain-helicase-DNA-binding protein 4Histone deacetylase inhibitorMetastasesOvarian cancerRomidepsin

Identifiers

PMID36681835
PMCPMC9862813
OpenAlexW4317605768

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.