Evidence map›Paper›PMID 30603114›Full record

ArticleSignal transduction and targeted therapy

miR-23a promotes invasion of glioblastoma

Kazuhiro Yachi, Masumi Tsuda, Shinji Kohsaka, Lei Wang, Yoshitaka Oda, Satoshi Tanikawa, Yusuke Ohba, Shinya Tanaka

Open access · goldAbstract read
In one paragraph

Article in Signal transduction and targeted therapy. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

43 citing papers in PubMed, 65 citations in OpenAlex.

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  17. The Role of MiRNA in Cancer: Pathogenesis, Diagnosis, and Treatment.Methods in molecular biology (Clifton, N.J.) · 2022
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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

8 authors at 2 institutions in 2 countries.

Kazuhiro Yachi *1Department of Cancer Pathology, Faculty of Medicine, Hokkaido University, Sapporo, Japan.
Masumi Tsuda *1Department of Cancer Pathology, Faculty of Medicine, Hokkaido University, Sapporo, Japan.
Shinji Kohsaka1Department of Cancer Pathology, Faculty of Medicine, Hokkaido University, Sapporo, Japan.
Lei Wang1Department of Cancer Pathology, Faculty of Medicine, Hokkaido University, Sapporo, Japan.
Yoshitaka Oda1Department of Cancer Pathology, Faculty of Medicine, Hokkaido University, Sapporo, Japan.
Satoshi Tanikawa1Department of Cancer Pathology, Faculty of Medicine, Hokkaido University, Sapporo, Japan.
Yusuke Ohba4Department of Cell Physiology, Faculty of Medicine, Hokkaido University, Sapporo, Japan.ORCID 0000-0003-2461-8289
Shinya Tanaka1Department of Cancer Pathology, Faculty of Medicine, Hokkaido University, Sapporo, Japan.
Sapporo University · JPHokkaido University of Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma is the most aggressive and invasive brain tumor and has a poor prognosis; elucidating the underlying molecular mechanisms is essential to select molecular targeted therapies. Here, we investigated the effect of microRNAs on the marked invasiveness of glioblastoma. U373 glioblastoma cells were infected with 140 different microRNAs from an OncomiR library, and the effects of the invasion-related microRNAs and targeted molecules were investigated after repeated Matrigel invasion assays. Screening of the OncomiR library identified miR-23a as a key regulator of glioblastoma invasion. In six glioblastoma cell lines, a positive correlation was detected between the expression levels of miR-23a and invasiveness. A luciferase reporter assay demonstrated that homeobox D10 (HOXD10) was a miR-23a-target molecule, which was verified by high scores from both the PicTar and miRanda algorithms. Forced expression of miR-23a induced expression of invasion-related molecules, including

Identifiers

PMID30603114
PMCPMC6308238
OpenAlexW2906362794

What OpenQuestion holds

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LicenceCC BY
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.