Evidence map›Paper›PMID 31190859›Full record

ArticleOncoTargets and therapy2019

miR-129-5p inhibits prostate cancer proliferation via targeting ETV1.

Ge Gao, Dianhui Xiu, Bin Yang, Daju Sun, Xin Wei, Youpeng Ding, Yanan Ma, Zhixin Wang

Open access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

23 citing papers in PubMed, 38 citations in OpenAlex.

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  6. Circ_103128 is associated with the tumorigenesis of medulloblastoma.Journal of cancer research and clinical oncology · 2023
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  11. Role of microRNA-129 in cancer and non-cancerous diseases (Review).Experimental and therapeutic medicine · 2021
    Review
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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

8 authors at 2 institutions in 1 country.

Ge GaoDepartment of Pathology, China-Japan Union Hospital of Jilin University, Changchun, Jilin 130033, P.R. China.
Dianhui XiuDepartment of Radiology, China-Japan Union Hospital of Jilin University, Changchun, Jilin 130033, P.R. China.
Bin YangDepartment of Breast Surgery, China-Japan Union Hospital of Jilin University, Changchun, Jilin 130033, P.R. China.
Daju SunDepartment of Pathology, China-Japan Union Hospital of Jilin University, Changchun, Jilin 130033, P.R. China.
Xin WeiDepartment of Urology, China-Japan Union Hospital of Jilin University, Changchun, Jilin 130033, P.R. China, wangzhixin1234@aliyun.com.
Youpeng DingDepartment of Urology, China-Japan Union Hospital of Jilin University, Changchun, Jilin 130033, P.R. China, wangzhixin1234@aliyun.com.
Yanan MaDepartment of Urology, China-Japan Union Hospital of Jilin University, Changchun, Jilin 130033, P.R. China, wangzhixin1234@aliyun.com.
Zhixin WangDepartment of Urology, China-Japan Union Hospital of Jilin University, Changchun, Jilin 130033, P.R. China, wangzhixin1234@aliyun.com.
Jilin University · CNUnion Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProstate cancer is one of the most commonly diagnosed diseases in males.

methodsRT-qPCR was used to detect miR-129-5p expression in tumor tissues and adjacent normal tissues from patients with prostate cancer. The cell proliferation assay and colony forming assay were used to study the role of miR-129-5p in mediating prostate cancer cell growth. Bioinformatic analysis and dual luciferase assay were performed to predict and confirm ETV1 as a target gene of miR-129-5p.

resultsWe found that miR-129-5p levels were decreased significantly in human prostate cancer tissues compared with matched normal tissues from patients with prostate cancer. Overexpression of miR-129-5p suppressed prostate cancer cell growth while antagonist of miR-129-5p promoted cell proliferation in immortal prostate cell line RWPE-1. In addition, elevation of miR-129-5p decreased ETV1 expression in prostate cancer cells while downregulation of miR-129-5p increased ETV1 expression in RWPE-1. Mechanistically, ETV1 is confirmed a direct target of miR-129-5p in prostate cancer cells. Through repression of ETV1 expression, miR-129-5p could inactivate YAP signaling in prostate cancer cells. In addition, overexpression of ETV1 attenuated miR-129-5p induced cell proliferation in prostate cancer cells. Correlation analysis further revealed that there was a negative correlation between miR-129-5p levels and ETV1 mRNA levels in tumor tissues from patients with prostate cancer.

conclusionOur results identified miR-129-5p as a tumor suppressor in prostate cancer via repression of ETV1.

Indexed as

ETV1microRNAproliferationprostate cancer

Identifiers

PMID31190859
PMCPMC6512784
OpenAlexW2944675891

What OpenQuestion holds

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LicenceCC BY-NC
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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.