Evidence map›Paper›PMID 28469953›Full record

ArticleAmerican journal of cancer research2017

MicroRNA-1468-5p inhibits glioma cell proliferation and induces cell cycle arrest by targeting RRM1.

Kuan Jiang, Tongle Zhi, Wenhui Xu, Xiupeng Xu, Weining Wu, Tianfu Yu, Er Nie, Xu Zhou, Zhongyuan Bao, Xin Jin and 3 more

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

20 citing papers in PubMed, 26 citations in OpenAlex.

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  13. LncRNA MALAT1/miR-129 axis promotes glioma tumorigenesis by targeting SOX2.Journal of cellular and molecular medicine · 2018
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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

13 authors at 2 institutions in 1 country.

Kuan JiangDepartment of Neurosurgery, The First Affiliated Hospital of Nanjing Medical UniversityNanjing 210000, Jiangsu Province, China.
Tongle ZhiDepartment of Neurosurgery, The First Affiliated Hospital of Nanjing Medical UniversityNanjing 210000, Jiangsu Province, China.
Wenhui XuDepartment of Neurosurgery, Yixing People's HospitalYixing 214200, Jiangsu Province, China.
Xiupeng XuDepartment of Neurosurgery, The First Affiliated Hospital of Nanjing Medical UniversityNanjing 210000, Jiangsu Province, China.
Weining WuDepartment of Neurosurgery, The First Affiliated Hospital of Nanjing Medical UniversityNanjing 210000, Jiangsu Province, China.
Tianfu YuDepartment of Neurosurgery, The First Affiliated Hospital of Nanjing Medical UniversityNanjing 210000, Jiangsu Province, China.
Er NieDepartment of Neurosurgery, The First Affiliated Hospital of Nanjing Medical UniversityNanjing 210000, Jiangsu Province, China.
Xu ZhouDepartment of Neurosurgery, The First Affiliated Hospital of Nanjing Medical UniversityNanjing 210000, Jiangsu Province, China.
Zhongyuan BaoDepartment of Neurosurgery, The First Affiliated Hospital of Nanjing Medical UniversityNanjing 210000, Jiangsu Province, China.
Xin JinDepartment of Neurosurgery, The First Affiliated Hospital of Nanjing Medical UniversityNanjing 210000, Jiangsu Province, China.
Junxia ZhangDepartment of Neurosurgery, The First Affiliated Hospital of Nanjing Medical UniversityNanjing 210000, Jiangsu Province, China.
Yingyi WangDepartment of Neurosurgery, The First Affiliated Hospital of Nanjing Medical UniversityNanjing 210000, Jiangsu Province, China.
Ning LiuDepartment of Neurosurgery, The First Affiliated Hospital of Nanjing Medical UniversityNanjing 210000, Jiangsu Province, China.
Nanjing Medical University · CNJiangsu University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs are associated with different types of cancers. In this study, we found that miR-1468-5p could inhibit growth and cell cycle progression in glioma by targeting ribonucleotide reductase large subunit M1 (RRM1). First, we analyzed miR-1468-5p expression in different glioma grades and the prognostic significance of its expression in glioblastoma multiform patients from the Chinese Glioma Genome Atlas. Then, we expressed miR-1468-5p in U87 and U251 cells and assessed the effects on proliferation and cell cycle progression using cell counting kit-8, colony formation, EdU and flow cytometry assays. Western blotting and luciferase reporter assays identified RRM1 as a novel direct target of miR-1468-5p. Experiments to determine the role of RRM1 in glioma showed that RRM1 expression was significantly higher in glioma than in normal brain tissues, and silencing RRM1 with small-interfering RNAs decreased proliferation and suppressed cell cycle progression, which indicated that RRM1 had pro-tumor functions. miR-1468-5p overexpression suppressed RRM1 expression, reduced glioma cell proliferation and induced cell cycle arrest, which was partially rescued by forced RRM1 expression. In summary, our study revealed that the regulatory mechanism of miR-1468-5p in glioma cell cycle progression involved direct regulation of RRM1 expression, suggesting that RRM1 may be a potential therapeutic target for glioma.

Indexed as

cell cyclegliomamiR-1468-5pproliferationRRM1

Identifiers

PMID28469953
PMCPMC5411788
OpenAlexW3023043413

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.