Evidence map›Paper›PMID 34779995›Full record

ArticleNeurochemical research2022

MiR-674-5p Suppresses the Proliferation and Migration of Glioma Cells by Targeting Cul4b.

Wen Li, Juan Liu, Li Ji, Yi Tang, Jianbing Qin, Heyan Zhao, Xiang Cheng, Meiling Tian, Guohua Jin, Hui He

Abstract read
PubMed Publisher
In one paragraph

Article in Neurochemical research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 56% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
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

10 authors at 1 institution in 1 country.

Wen LiDepartment of Human Anatomy, Medical School, Nantong University, Nantong, Jiangsu, People's Republic of China.ORCID http://orcid.org/0000-0003-2402-6769
Juan LiuDepartment of Human Anatomy, Medical School, Nantong University, Nantong, Jiangsu, People's Republic of China.
Li JiDepartment of Human Anatomy, Medical School, Nantong University, Nantong, Jiangsu, People's Republic of China.
Yi TangDepartment 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.
Heyan ZhaoDepartment of Human Anatomy, Medical School, Nantong University, Nantong, Jiangsu, People's Republic of China.
Xiang ChengDepartment of Human Anatomy, Medical School, Nantong University, Nantong, Jiangsu, People's Republic of China.
Meiling TianDepartment 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
Hui HeDepartment of Human Anatomy, Medical School, Nantong University, Nantong, Jiangsu, People's Republic of China. hehui87@ntu.edu.cn.ORCID http://orcid.org/0000-0001-8164-4382
Nantong University · CN

Funding

the Priority Academic Program Development (PAPD) of Jiangsu Higher Education Institutions 03081023the Science and Technology Program of Nantong City JC2020024
6 · The paper itself

Abstract

Glioma multiforme (GBM) is the most common malignant primary brain tumors. Despite the considerable advances in GBM treatment, it is still one of the most lethal forms of brain tumor. New clinical biomarkers and therapeutic targets are immediately required. MicroRNAs (miRNAs) are a class of small, evolutionarily conserved noncoding RNAs and have emerged as the key regulators of many cancers. Here in this study, we showed that miR-674-5p was probably an important regulator of glioma cell growth. After the transfection with miR-674-5p mimic or inhibitor, we found that the expression level of miR-674-5p was negatively related with cell proliferation and migration in C6 cells. Based on the prediction of the target genes of miR-674-5p on the website, we chose Cullin 4B (Cul4b), a gene upregulated in GBM, and proved that it was a target of miR-674-5p. In addition, we explored the role of miR-674-5p in glioma growth in vivo. Taken together, the present study indicated that miR-674-5p suppressed glioma cell proliferation and migration by targeting Cul4b.

Indexed as

Brain NeoplasmsCullin ProteinsGliomaMicroRNAsAnimalsCell Line, TumorCell MovementCell ProliferationGene Expression Regulation, NeoplasticRatsCullin ProteinsMicroRNAsCul4bGliomaMigrationmiR-674-5pProliferation

Identifiers

PMID34779995
OpenAlexW3211550624

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.