Evidence map›Paper›PMID 30896817›Full record

ArticleMolecular medicine reports2019

miR‑512‑5p suppresses proliferation, migration and invasion, and induces apoptosis in non‑small cell lung cancer cells by targeting ETS1.

Bin Cao, Sheng Tan, Huijuan Tang, Yihui Chen, Peng Shu

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2019. 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
1.1field-weighted citation impact, top 28% 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, 22 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

5 authors at 3 institutions in 1 country.

Bin CaoDepartment of Cardiothoracic Surgery, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, Jiangsu 210005, P.R. China.
Sheng TanDepartment of Cardio‑Thoracic Surgery, The Affiliated Hospital of Xuzhou Medical College, Xuzhou, Jiangsu 221000, P.R. China.
Huijuan TangDepartment of Oncology, Jiangsu Provincial Hospital of Traditional Chinese Medicine, Nanjing, Jiangsu 210005, P.R. China.
Yihui ChenDepartment of Oncology, Jiangsu Provincial Hospital of Traditional Chinese Medicine, Nanjing, Jiangsu 210005, P.R. China.
Peng ShuDepartment of Oncology, Jiangsu Provincial Hospital of Traditional Chinese Medicine, Nanjing, Jiangsu 210005, P.R. China.
Jiangsu Provincial Hospital of Traditional Chinese Medicine · CNAffiliated Hospital of Xuzhou Medical College · CNNanjing Drum Tower Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An increasing number of microRNA (miRNA) have been demonstrated to serve as molecular biomarkers for tumor cell progression. miR‑512‑5p was revealed as oncogenic regulator in several types of cancer. However, whether and how miR‑512‑5p regulates non‑small cell lung cancer (NSCLC) remains unclear. In the present study, the expression of miR‑512‑5p was detected in NSCLC tissues and cell lines. Then, the proliferation, migration, invasion and apoptosis in NSCLC A549 and H1299 cell lines were detected when miR‑512‑5p was overexpressed. Furthermore, the underlying mechanism was identified. The level of miR‑512‑5p was decreased in NSCLC tissues and in NSCLC cells compared with adjacent normal tissues and normal lung tissue cell lines. miR‑512‑5p mimics inhibited the cell proliferation, migration, invasion and induced apoptosis in A549 and H1299 cells. In addition, a luciferase reporter assay suggested that overexpression of miR‑512‑5p may decrease the expression of the E26 transformation specific‑1 (ETS1) gene; it was subsequently verified that downregulation of the ETS1 gene inhibited cell proliferation and migration and induced cell apoptosis in A549 and H1299 cells, and ETS1 small interfering RNA in the presence of an miR‑512‑5p inhibitor reversed the effect. The data described in the present study suggest that miR‑512‑5p may be a tumor suppressor and a potential treatment target in NSCLC.

Indexed as

Gene Expression Regulation, NeoplasticRNA Interference3' Untranslated RegionsApoptosisCarcinoma, Non-Small-Cell LungCell Line, TumorCell MovementCell ProliferationGene Knockdown TechniquesHumansLung NeoplasmsMicroRNAsProto-Oncogene Protein c-ets-13' Untranslated RegionsETS1 protein, humanMicroRNAsMIRN512 microRNA, humanProto-Oncogene Protein c-ets-1

Identifiers

PMID30896817
PMCPMC6471623
OpenAlexW2922005956

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.