Evidence map›Paper›PMID 34253194›Full record

ArticleWorld journal of surgical oncology2021

MiR-186-3p attenuates tumorigenesis of cervical cancer by targeting IGF1.

Xiurong Lu, Xiao Song, Xiaohui Hao, Xiaoyu Liu, Xianyu Zhang, Na Yuan, Huan Ma, Zhilin Zhang

Open access · goldAbstract read
In one paragraph

Article in World journal of surgical oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 18% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 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

8 authors at 1 institution in 1 country.

Xiurong LuDepartment of Radiotherapy, The First Affiliated Hospital of Hebei North University, No. 36, Changqing Road, Zhangjiakou, 075000, Hebei, China. xiurong_lu2@163.com.ORCID http://orcid.org/0000-0001-8531-1219
Xiao SongDepartment of Radiotherapy, The First Affiliated Hospital of Hebei North University, No. 36, Changqing Road, Zhangjiakou, 075000, Hebei, China.
Xiaohui HaoDepartment of Radiotherapy, The First Affiliated Hospital of Hebei North University, No. 36, Changqing Road, Zhangjiakou, 075000, Hebei, China.
Xiaoyu LiuDepartment of Radiotherapy, The First Affiliated Hospital of Hebei North University, No. 36, Changqing Road, Zhangjiakou, 075000, Hebei, China.
Xianyu ZhangDepartment of Radiotherapy, The First Affiliated Hospital of Hebei North University, No. 36, Changqing Road, Zhangjiakou, 075000, Hebei, China.
Na YuanDepartment of Radiotherapy, The First Affiliated Hospital of Hebei North University, No. 36, Changqing Road, Zhangjiakou, 075000, Hebei, China.
Huan MaDepartment of Radiotherapy, The First Affiliated Hospital of Hebei North University, No. 36, Changqing Road, Zhangjiakou, 075000, Hebei, China.
Zhilin ZhangDepartment of Radiotherapy, The First Affiliated Hospital of Hebei North University, No. 36, Changqing Road, Zhangjiakou, 075000, Hebei, China.
Hebei North University · CN

Funding

Zhangjiakou City's 2020 Municipal Science and Technology Plan Self-financing Project 2021053D
6 · The paper itself

Abstract

backgroundMounting evidence in the cancer literature suggests that microRNAs (miRNAs) influence the progression of human cancer cells by targeting protein-coding genes. How insulin-like growth factor 1(IGF1) and miR-186-3p contribute to the development of cervical cancer (CC) remains unclear. This study examined the regulatory roles of miR-186-3p and IGF1 in CC development.

methodsGene expression levels were determined by qRT-PCR. Proliferation, migration, and apoptosis of CC and normal cells were determined by MTT, Transwell, and caspase-3 activity assays, respectively. Dual-luciferase reporter activity and RNA pull-down assays were performed to identify the target gene of miR-186-3p.

resultsIGF1 was the target of miR-186-3p. The expression of miR-186-3p inhibited cell proliferation and migration abilities of CC cell lines, but induced the apoptosis rate of CC cells. IGF1 could restore the inhibitory effects of miR-186-3p on the proliferation, migration, and apoptosis abilities of CC cells. Experimental results revealed that miR-186-3p could inhibit IGF1 expression, thereby reducing the viability of CC cells.

conclusionsThe data suggest that targeting of IGF1 by miR-186-3p could be crucial in regulating the progression of CC.

Indexed as

MicroRNAsUterine Cervical NeoplasmsApoptosisCarcinogenesisCell Line, TumorCell MovementCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansInsulin-Like Growth Factor IPrognosisIGF1 protein, humanInsulin-Like Growth Factor IMicroRNAsMIRN186 microRNA, humanApoptosisCervical cancerIGF1MigrationmiR-186-3pProliferation

Identifiers

PMID34253194
PMCPMC8276452
OpenAlexW3180549123

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.