Evidence map›Paper›PMID 28423357›Full record

ArticleOncotarget2017

MiR-29b inhibits the growth of glioma via MYCN dependent way.

Guan Sun, Jingmin Lu, Chuang Zhang, Ran You, Lei Shi, Nan Jiang, Dekang Nie, Jian Zhu, Min Li, Jun Guo

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 34% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
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  8. Serum miR-29b as a novel biomarker for glioblastoma diagnosis and prognosis.International journal of clinical and experimental pathology · 2019
    Article
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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 7 institutions in 1 country.

Guan SunDepartment of Neurosurgery, First People's Hospital of Yancheng, Fourth Affiliated Hospital of Nantong University, Yancheng, 224001, PR China.
Jingmin LuDepartment of Neurology, The Affiliated Huai'an Hospital of Xuzhou Medical University and The Second People's Hospital of Huai'an, Huai'an, 223001, PR China.
Chuang ZhangDepartment of Medical Oncology, The 81st Hospital of People's Liberation Army, Nanjing, 210002, PR China.
Ran YouDepartment of Interventional Radiology, Nantong University Affiliated Hospital, Nantong, 226000, PR China.
Lei ShiDepartment of Neurosurgery, The First People's Hospital of Kunshan Affiliated with Jiangsu University, Suzhou, 215300, PR China.
Nan JiangDepartment of Neurosurgery, First People's Hospital of Yancheng, Fourth Affiliated Hospital of Nantong University, Yancheng, 224001, PR China.
Dekang NieDepartment of Neurosurgery, First People's Hospital of Yancheng, Fourth Affiliated Hospital of Nantong University, Yancheng, 224001, PR China.
Jian ZhuDepartment of Neurosurgery, First People's Hospital of Yancheng, Fourth Affiliated Hospital of Nantong University, Yancheng, 224001, PR China.
Min LiDepartment of Neurosurgery, Jiangning Hospital Affiliated with Nanjing Medical University, Nanjing, 211100, PR China.
Jun GuoDepartment of Neurosurgery, First People's Hospital of Yancheng, Fourth Affiliated Hospital of Nantong University, Yancheng, 224001, PR China.
Affiliated Hospital of Nantong University · CNNantong University · CN181st Hospital of Chinese People's Liberation Army · CNFirst People's Hospital of Kunshan · CNNanjing Medical University · CNSecond People’s Hospital of Huai’an · CNYancheng First People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MiR-29b is widely involved in diverse cancers. We plan to study its role in glioma. The expression of miR-29b was detected by real-time polymerase chain reaction (PCR) and we found the expression of miR-29b was decreased in glioma. Cell proliferation was evaluated by cell counting kit (CCK8) and 5-Ethynyl-2'- deoxyuridine (EdU) and cell apoptosis was assayed with flow cytometry assay (FCA), which indicated miR-29b can inhibit the proliferation and promote the apoptosis of glioma cells. The target of miR-29b was predicted using miRanda, TargetScan and PicTar sofeware and we also found MYCN was a direct target of miR-29b in glioma cells and miR-29b inhibited the proliferation of glioma cells via MYCN dependent way. Subcutaneous xenotransplantation model was designed to investigate the affection of miR-29b on glioma growth. The effectiveness of miR-29b for glioma prediction was also performed and we determined miR-29b can stably exist and may act as a biomarker for the diagnosis of glioma. As a conclusion, miR-29b inhibits the growth of glioma via MYCN dependent way and can be a biomarker for the diagnosis of glioma.

Indexed as

AnimalsBrain NeoplasmsCell Growth ProcessesCell Line, TumorFemaleGliomaHeterograftsHumansMaleMice, Inbred BALB CMice, NudeMicroRNAsMiddle AgedN-Myc Proto-Oncogene ProteinMicroRNAsMIRN29a microRNA, humanMYCN protein, humanN-Myc Proto-Oncogene ProteingliomamiR-29bMYCN

Identifiers

PMID28423357
PMCPMC5542180
OpenAlexW2598763231

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.