Evidence map›Paper›PMID 31497204›Full record

ArticleAmerican journal of translational research2019

MicroRNA-940 inhibits glioma cells proliferation and cell cycle progression by targeting CKS1.

Hui Luo, Ran Xu, Binglin Chen, Shiyang Dong, Fengqi Zhou, Tianfu Yu, Guanhua Xu, Junxia Zhang, Yingyi Wang, Yongping You

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

23 citing papers in PubMed, 29 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

10 authors at 2 institutions in 1 country.

Hui LuoDepartment of Neurosurgery, The First Affiliated Hospital of Nanjing Medical University Nanjing, China.
Ran XuDepartment of Neurosurgery, The First Affiliated Hospital of Nanjing Medical University Nanjing, China.
Binglin ChenDepartment of Neurosurgery, The First Affiliated Hospital of Nanjing Medical University Nanjing, China.
Shiyang DongDepartment of Anesthesiology, The First Affiliated Hospital of Nanjing Medical University Nanjing, China.
Fengqi ZhouDepartment of Neurosurgery, The First Affiliated Hospital of Nanjing Medical University Nanjing, China.
Tianfu YuDepartment of Neurosurgery, The First Affiliated Hospital of Nanjing Medical University Nanjing, China.
Guanhua XuDepartment of Neurosurgery, The First Affiliated Hospital of Nanjing Medical University Nanjing, China.
Junxia ZhangDepartment of Neurosurgery, The First Affiliated Hospital of Nanjing Medical University Nanjing, China.
Yingyi WangDepartment of Neurosurgery, The First Affiliated Hospital of Nanjing Medical University Nanjing, China.
Yongping YouDepartment of Neurosurgery, The First Affiliated Hospital of Nanjing Medical University Nanjing, China.
Jiangsu Province Hospital · CNNanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma (GBM) is the most frequently occurred malignant human tumor that arise in brain with a poor prognosis. microRNAs (miRNAs) are vital small molecules during GBM initiation and progression. However, the expression of miR-940 and its potential function in GBM remain poor. Our study demonstrated that miR-940 was dramatically decreased in GBM cells and glioma tissues. Introduction of miR-940 significantly repressed proliferative ability of GBM cells. Notably, treatment of miR-940 dramatically suppressed tumor growth in an animal model, accompanied by decreased Ki67 expression. Functional experiments showed CKS1 as a target of miR-940, knockdown of CKS1 significantly induced the cell cycle arrest and restrained GBM cells proliferation, consistent with miR-940 treatment. Furthermore, reintroduction of CKS1 into glioma cells effectively rescued the tumor suppressive effect of miR-940. Correlation analysis indicated that miR-940 expression was inversely related to CKS1 mRNA levels in NBTs and gliomas. Together, miR-940/CKS1 signaling may be required for GBM progression and provide a new insight in diagnosis and prognosis of GBM patients.

Indexed as

CKS1gliomamiR-940proliferation

Identifiers

PMID31497204
PMCPMC6731435
OpenAlexW2992283979

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.