Evidence map›Paper›PMID 32388695›Full record

ArticleNeurochemical research2020

MiR-210-3p Inhibits Proliferation and Migration of C6 Cells by Targeting Iscu.

Hui He, Juan Liu, Wen Li, Xiang Yao, Qiqi Ren, Beilei Shen, Cheng Xue, Linqing Zou, Heyan Zhao, Jianbing Qin and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Neurochemical research, 2020. 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
0.4field-weighted citation impact, top 47% 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, 10 citations in OpenAlex.

  1. Pooled it
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  5. 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

11 authors at 1 institution in 1 country.

Hui HeDepartment of Human Anatomy, Medical School, Nantong University, Nantong, Jiangsu, People's Republic of China.ORCID http://orcid.org/0000-0001-8164-4382
Juan LiuDepartment of Human Anatomy, Medical School, Nantong University, Nantong, Jiangsu, People's Republic of China.
Wen LiDepartment of Human Anatomy, Medical School, Nantong University, Nantong, Jiangsu, People's Republic of China.
Xiang YaoDepartment of Human Anatomy, Medical School, Nantong University, Nantong, Jiangsu, People's Republic of China.
Qiqi RenDepartment of Human Anatomy, Medical School, Nantong University, Nantong, Jiangsu, People's Republic of China.
Beilei ShenDepartment of Human Anatomy, Medical School, Nantong University, Nantong, Jiangsu, People's Republic of China.
Cheng XueDepartment of Human Anatomy, Medical School, Nantong University, Nantong, Jiangsu, People's Republic of China.
Linqing ZouDepartment of Human Anatomy, Medical School, Nantong University, Nantong, Jiangsu, People's Republic of China.
Heyan ZhaoDepartment of Human Anatomy, Medical School, Nantong University, Nantong, Jiangsu, People's Republic of China.
Jianbing QinDepartment of Human Anatomy, Medical School, Nantong University, Nantong, Jiangsu, People's Republic of China.
Guohua JinDepartment of Human Anatomy, Medical School, Nantong University, Nantong, Jiangsu, People's Republic of China. jguohua@ntu.edu.cn.ORCID http://orcid.org/0000-0001-7853-2574
Nantong University · CN

Funding

Natural Science Foundation of Jiangsu Province BK20170447Undergraduate Innovation Training Program of Nantong University 2019141
6 · The paper itself

Abstract

Glioma is the most common primary brain tumor and the most malignant type of glioma is glioblastoma with the character of high mortality, high recurrence rate and poor prognosis. MicroRNAs act as an important component in glioma development and thus may be a potential target for the treatment of glioma. There were some researches indicated that miR-210-3p played a role in glioma development, but if it can inhibit glioma growth, as well as the underlying mechanism, is still uncertain. In the present study, we investigated the effects of miR-210-3p and its potential target gene Iscu on glioma (C6) cells proliferation and migration in vitro as well as the influence of miR-210-3p on glioma growth in vivo. The results showed that miR-210-3p inhibited the proliferation and migration of C6 cells by regulating the expression of its target gene Iscu in vitro. We also demonstrated that glioma growth was suppressed in immunodeficient mice when they were implanted with C6 cells overexpressing miR-210-3p. Our data indicated that miR-210-3p played an important role in the prevention of glioma growth by targeting Iscu and so miR-210-3p/Iscu axis might be a potential target for the treatment of glioma.

Indexed as

AnimalsCell Line, TumorCell MovementCell ProliferationGene Expression Regulation, NeoplasticGene Knockdown TechniquesGliomaIron-Sulfur ProteinsMice, Inbred BALB CMice, NudeMicroRNAsRatsIron-Sulfur ProteinsIscu protein, ratMicroRNAsMIRN210 microRNA, ratGliomaIscuMigrationmiR-210-3pProliferation

Identifiers

PMID32388695
OpenAlexW3023889570

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.