Evidence map›Paper›PMID 31068580›Full record

ArticleCell death & disease2019

miR-340-FHL2 axis inhibits cell growth and metastasis in ovarian cancer.

Zheng Huang, Qiuxia Li, Kaili Luo, Qinkai Zhang, Jingwen Geng, Xunzhu Zhou, Yesha Xu, Mengyao Qian, Jian-An Zhang, Liying Ji and 1 more

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in Cell death & disease, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.6field-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

30 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
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  8. The roles of FHL2 in cancer.Clinical and experimental medicine · 2023
    Review
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  11. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Zheng HuangInstitute of Genomic Medicine, Wenzhou Medical University, 325000, Wenzhou, Zhejiang, P. R. China.
Qiuxia LiInstitute of Genomic Medicine, Wenzhou Medical University, 325000, Wenzhou, Zhejiang, P. R. China.
Kaili LuoInstitute of Genomic Medicine, Wenzhou Medical University, 325000, Wenzhou, Zhejiang, P. R. China.
Qinkai ZhangInstitute of Genomic Medicine, Wenzhou Medical University, 325000, Wenzhou, Zhejiang, P. R. China.
Jingwen GengInstitute of Genomic Medicine, Wenzhou Medical University, 325000, Wenzhou, Zhejiang, P. R. China.
Xunzhu ZhouInstitute of Genomic Medicine, Wenzhou Medical University, 325000, Wenzhou, Zhejiang, P. R. China.
Yesha XuInstitute of Genomic Medicine, Wenzhou Medical University, 325000, Wenzhou, Zhejiang, P. R. China.
Mengyao QianInstitute of Genomic Medicine, Wenzhou Medical University, 325000, Wenzhou, Zhejiang, P. R. China.
Jian-An ZhangDepartment of Obstetrics and Gynecology, The Second Affiliated Hospital and Yuying Children of Wenzhou Medical University, 325027, Wenzhou, Zhejiang, P. R. China.
Liying JiInstitute of Genomic Medicine, Wenzhou Medical University, 325000, Wenzhou, Zhejiang, P. R. China.
Jianmin WuInstitute of Genomic Medicine, Wenzhou Medical University, 325000, Wenzhou, Zhejiang, P. R. China. Jianminwu81@hotmail.com.
Wenzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although increasing evidence indicated that deregulation of microRNAs (miRNAs) contributed to tumor initiation and progression, but little is known about the biological role of miR-340 in ovarian cancer (OC). In this study, we found that miR-340 expression was downregulated in OC tissues compared with its expression in normal ovarian epithelium and endometrium, and treatment with 5-aza-2'-deoxycytidine (5-Aza-dC) or trichostatin A (TSA) increased miR-340 expression in OC cells. In addition, ectopic miR-340 expression inhibited OC cell growth and metastasis in vitro and in vivo. Four and a half LIM domains protein 2 (FHL2) was confirmed as a direct target of miR-340 and silencing FHL2 mimicked the effects of miR-340 in OC cells. Further mechanistic study showed that miR-340 inhibited the Wnt/β-catenin pathway by targeting FHL2, as well as downstream cell cycle and epithelial-to-mesenchymal transition (EMT) signals in OC cells. Moreover, the greatest association between miR-340 and FHL2 was found in 481 ovarian serous cystadenocarcinoma tissues via pan-cancer analysis. Finally, we revealed that lower miR-340 or higher FHL2 was associated with poor OC patient outcomes. Our findings indicate that the miR-340-FHL2 axis regulates Wnt/β-catenin signaling and is involved in tumorigenesis in OC. Therefore, manipulating the expression of miR-340 or its target genes is a potential strategy in OC therapy.

Indexed as

Cell Proliferation3' Untranslated RegionsAnimalsCell Line, TumorCell MovementCystadenocarcinomaDown-RegulationEpithelial-Mesenchymal TransitionFemaleHumansLIM-Homeodomain ProteinsMiceMice, NudeMicroRNAsMuscle ProteinsOvarian Neoplasms3' Untranslated RegionsFHL2 protein, humanLIM-Homeodomain ProteinsMicroRNAsMIRN340 microRNA, humanMuscle ProteinsRNA, Small InterferingTranscription Factors

Identifiers

PMID31068580
PMCPMC6506554
OpenAlexW2944383857

What OpenQuestion 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 OpenQuestion graph.