Evidence map›Paper›PMID 30774377›Full record

ArticleOncoTargets and therapy2019

microRNA-628 inhibits the proliferation of acute myeloid leukemia cells by directly targeting IGF-1R.

Lu Chen, Xin Jiang, Haoyue Chen, Qiaoyan Han, Chunhua Liu, Miao Sun

RetractedOpen access · goldAbstract readRetracted Publication
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. It has been retracted, and should not be counted. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 26% 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, 19 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Lu ChenDepartment of Hematology, Jingjiang People's Hospital, The Seventh Affiliated Hospital of Yangzhou University, Jiangsu 214500, P.R. China, liuyunyang6@126.com; miao_sun01@163.com.
Xin JiangDepartment of Hematology, Jingjiang People's Hospital, The Seventh Affiliated Hospital of Yangzhou University, Jiangsu 214500, P.R. China, liuyunyang6@126.com; miao_sun01@163.com.
Haoyue ChenDepartment of Hematology, Jingjiang People's Hospital, The Seventh Affiliated Hospital of Yangzhou University, Jiangsu 214500, P.R. China, liuyunyang6@126.com; miao_sun01@163.com.
Qiaoyan HanDepartment of Hematology, Jingjiang People's Hospital, The Seventh Affiliated Hospital of Yangzhou University, Jiangsu 214500, P.R. China, liuyunyang6@126.com; miao_sun01@163.com.
Chunhua LiuDepartment of Hematology, Jingjiang People's Hospital, The Seventh Affiliated Hospital of Yangzhou University, Jiangsu 214500, P.R. China, liuyunyang6@126.com; miao_sun01@163.com.
Miao SunDepartment of Hematology, Jingjiang People's Hospital, The Seventh Affiliated Hospital of Yangzhou University, Jiangsu 214500, P.R. China, liuyunyang6@126.com; miao_sun01@163.com.
Yangzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA variety of microRNAs (miRNAs) are aberrantly expressed in acute myeloid leukemia (AML), and these dysregulated miRNAs perform crucial roles in tumorigenesis and progression of AML. miR-628-3p (miR-628), one of the miRNAs dysregulated in multiple types of human cancers, exerts antitumor roles in different cancer types. However, no specific study has explored the expression pattern and role of miR-628 in AML. MATERIALS AND

methodsIn this study, RT-qPCR was performed to detect miR-628 expression in AML tissues and cell lines. CCK-8 assay, flow cytometry analysis and xenograft tumor experiment was carried out to determine the functions of miR-628 in AML cells. The possible mechanism underlying the activity of miR-628 in AML cells was also explored using a series of experiments.

resultsOur results revealed the downregulated expression of miR-628 in patients with AML and AML cell lines. Ectopic expression of miR-628 resulted in the inhibition of AML cell proliferation and induction of cell cycle arrest and apoptosis in vitro and attenuation of tumor growth in vivo. Insulin-like growth factor 1 receptor (

conclusionOur results demonstrate that miR-628 exhibits antitumor effects in AML through the direct targeting of

Indexed as

acute myeloid leukemiaapoptosiscell cycleinsulin-like growth factor 1 receptormicroRNA-628PI3K/Akt pathwayproliferation

Identifiers

PMID30774377
PMCPMC6357892
OpenAlexW2912767778

What OpenQuestion holds

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LicenceCC BY-NC
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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.