Evidence map›Paper›PMID 25895125›Full record

ArticleOncotarget2015

A novel role for microRNA-129-5p in inhibiting ovarian cancer cell proliferation and survival via direct suppression of transcriptional co-activators YAP and TAZ.

Guosheng Tan, Xinping Cao, Qiangsheng Dai, Bing Zhang, Jianwen Huang, Shiqiu Xiong, Yong yu Zhang, Wei Chen, Jianyong Yang, Heping Li

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
6.8field-weighted citation impact, top 2% 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

43 citing papers in PubMed, 73 citations in OpenAlex.

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  11. Role of microRNA-129 in cancer and non-cancerous diseases (Review).Experimental and therapeutic medicine · 2021
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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

10 authors at 4 institutions in 2 countries.

Guosheng TanDepartment of Interventional Radiology, the First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Xinping CaoDepartment of Radiotherapy, Sun Yat-sen University Cancer Center, Guangzhou, China.
Qiangsheng DaiDepartment of Medical Oncology, the First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Bing ZhangDepartment of Nuclear Medicine, the First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Jianwen HuangDepartment of Radiation Oncology, the First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Shiqiu XiongDepartment of Biochemistry, University of Leicester, Leicester, UK.
Yong yu ZhangDepartment of Interventional Radiology, the First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Wei ChenDepartment of Interventional Radiology, the First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Jianyong YangDepartment of Interventional Radiology, the First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Heping LiDepartment of Interventional Radiology, the First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Sun Yat-sen University · CNThe First Affiliated Hospital, Sun Yat-sen University · CNSun Yat-sen University Cancer Center · CNUniversity of Leicester · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transcriptional co-activator Yes-associated protein (YAP) and transcriptional co-activator with PDZ-binding motif (TAZ) are key oncogenes in mammalian cells. Activities of YAP and TAZ are largely restricted by the Hippo tumor suppressor pathway through phosphorylation-ubiquitination mechanisms. The involvement of microRNA in cancer progression has recently been reported, though whether they have a role in activating YAP and TAZ in human cancer cells remains unclear. Here, we report a microRNA, miR-129-5p, directly represses YAP and TAZ expression, leading to the inactivation of TEA domain (TEAD) transcription, and the downregulation of Hippo downstream genes, connective tissue growth factor (CTGF) and Cyclin A. Furthermore, we reveal miR-129-5p inhibits ovarian cancer cell proliferation, survival and tumorigenicity, and that downregulation of miR-129-5p in ovarian cancer cells highly correlates with malignant progression and poor survival. Hence, we demonstrate a novel mechanism for YAP and TAZ activation in cancers, indicating not only a potentially pivotal role for miR-129-5p in the progression of ovarian cancer, but also offering new therapeutic strategies to circumvent the disease.

Indexed as

Adaptor Proteins, Signal TransducingAdultAgedAnimalsCell Line, TumorConnective Tissue Growth FactorCyclin ADisease ProgressionDown-RegulationFemaleGene Expression Regulation, NeoplasticHeterograftsHippo Signaling PathwayHumansIntracellular Signaling Peptides and ProteinsMiceAdaptor Proteins, Signal TransducingCCN2 protein, humanConnective Tissue Growth FactorCyclin AIntracellular Signaling Peptides and ProteinsMicroRNAsMirn129 microRNA, humanOligonucleotidesPhosphoproteinsProtein Serine-Threonine KinasesRNA, MessengerRNA, NeoplasmRNA, Small InterferingTrans-ActivatorsTranscriptional Coactivator with PDZ-Binding Motif ProteinsTranscription FactorsWWTR1 protein, humanYAP1 protein, humanYAP-Signaling Proteinscell proliferationmiR-129-5psurvivalTAZYAP

Identifiers

PMID25895125
PMCPMC4496175
OpenAlexW2096125864

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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.