Evidence map›Paper›PMID 31218100›Full record

ArticleAmerican journal of cancer research2019

Overexpression of MEF2D contributes to oncogenic malignancy and chemotherapeutic resistance in ovarian carcinoma.

Xiaoxue Li, Yongjing Zhang, Xiaoshan Chai, Shuhua Zhou, Hongbo Zhang, Jie He, Ruiqiong Zhou, Lan Cai, Lin Chen, Guangshi Tao

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

14 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Long non-coding RNAs: Key regulators of stemness in breast cancer.Frontiers in cell and developmental biology · 2025
    Review
  6. Article
  7. MEF2D Functions as a Tumor Suppressor in Breast Cancer.International journal of molecular sciences · 2024
    Article
  8. The Molecular and Biological Function of MEF2D in Leukemia.Advances in experimental medicine and biology · 2024
    Review
  9. Observational
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
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

10 authors at 3 institutions in 2 countries.

Xiaoxue LiDepartment of Obstetrics and Gynecology, The Second Xiang Ya Hospital of Central South University Changsha 410011, China.
Yongjing ZhangDepartment of Obstetrics and Gynecology, The Second Xiang Ya Hospital of Central South University Changsha 410011, China.
Xiaoshan ChaiDepartment of Obstetrics and Gynecology, The Second Xiang Ya Hospital of Central South University Changsha 410011, China.
Shuhua ZhouDepartment of Obstetrics and Gynecology, The Second Xiang Ya Hospital of Central South University Changsha 410011, China.
Hongbo ZhangDepartment of Pathology, The Second Xiang Ya Hospital of Central South University Changsha 410011, China.
Jie HeDepartment of Gynecology Oncology, The Hunan Province Cancer Hospital Changsha 410013, China.
Ruiqiong ZhouDepartment of Obstetrics and Gynecology, The Second Xiang Ya Hospital of Central South University Changsha 410011, China.
Lan CaiDepartment of Obstetrics and Gynecology, The Second Xiang Ya Hospital of Central South University Changsha 410011, China.
Lin ChenDepartment of Chemistry and Biological Sciences, University of Southern California 1050 Childs Way, RRI 204c, Los Angeles 90089, CA, USA.
Guangshi TaoDepartment of Obstetrics and Gynecology, The Second Xiang Ya Hospital of Central South University Changsha 410011, China.
Central South University · CNHunan Cancer Hospital · CNUniversity of Southern California · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The transcription factor MEF2 promotes survival in various cell types and a number of studies indicate that abnormal regulation of MEF2 is linked to oncogenicity in several carcinomas. We have found that MEF2D, a member of the MEF2 family, is upregulated in Ovarian Cancer (OC). Immunohistochemistry analysis of tumor sections of 402 OC patients revealed that MEF2D is significantly elevated at the protein level. We have also found that the expression level of MEF2D is associated with cisplatin-resistance and poor prognosis by a retrospective analysis. Furthermore, Downregulation of MEF2D by siRNA reduces proliferation and invasiveness of OC cells SKOV3 and OVCAR3, induces apoptosis in vitro, and abolishes OVCAR3 tumorigenicity in xenograft model. Mechanistic study via ChIP analysis identified two of MEF2D-targeted genes, HPSE and IKBKE, which are associated with tumor invasion and chemotherapy-resistance, in accord with MEF2D expression in OC. Remarkably, knock-down of MEF2D invariably lead to the downregulation of IKBKE and reversed cisplatin (DDP)-resistance in cisplatin-resistant cells SKOV3-DDP. Our results suggest that MEF2D promotes malignant biological behaviors and cisplatin-resistance in OC and establish MEF2D as a new therapeutic target in OC treatment.

Indexed as

cisplatin-resistantHPSEIKBKEMEF2DOvarian cancer (OC)

Identifiers

PMID31218100
PMCPMC6556600
OpenAlexW2985789331

What OpenQuestion holds

Textmetadata
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.