Evidence map›Paper›PMID 30214063›Full record

ArticleScientific reports2018

Suppression of GPR56 expression by pyrrole-imidazole polyamide represents a novel therapeutic drug for AML with high EVI1 expression.

Hasi Rani Saha, Kazuko Kaneda-Nakashima, Shunsuke Shimosaki, Akira Suekane, Bidhan Sarkar, Yusuke Saito, Honami Ogoh, Shingo Nakahata, Kentaro Inoue, Takayoshi Watanabe and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-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

12 citing papers in PubMed, 16 citations in OpenAlex.

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  6. Culturing patient-derived malignant hematopoietic stem cells in engineered and fully humanized 3D niches.Proceedings of the National Academy of Sciences of the United States of America · 2021
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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

12 authors at 2 institutions in 1 country.

Hasi Rani SahaDivision of Tumor and Cellular Biochemistry, Department of Medical Sciences, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
Kazuko Kaneda-NakashimaDivision of Tumor and Cellular Biochemistry, Department of Medical Sciences, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
Shunsuke ShimosakiDivision of Tumor and Cellular Biochemistry, Department of Medical Sciences, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
Akira SuekaneDivision of Tumor and Cellular Biochemistry, Department of Medical Sciences, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
Bidhan SarkarDivision of Tumor and Cellular Biochemistry, Department of Medical Sciences, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
Yusuke SaitoDivision of Tumor and Cellular Biochemistry, Department of Medical Sciences, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
Honami OgohDivision of Tumor and Cellular Biochemistry, Department of Medical Sciences, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
Shingo NakahataDivision of Tumor and Cellular Biochemistry, Department of Medical Sciences, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
Kentaro InoueDepartment of Computer Science and Systems Engineering, Faculty of Engineering, University of Miyazaki, Miyazaki, Japan.
Takayoshi WatanabeDivision of Innovative Cancer Therapeutics, Chiba Cancer Center Research Institute, Chiba, Japan.
Hiroki NagaseDivision of Innovative Cancer Therapeutics, Chiba Cancer Center Research Institute, Chiba, Japan.ORCID 0000-0002-3992-5399
Kazuhiro MorishitaDivision of Tumor and Cellular Biochemistry, Department of Medical Sciences, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan. kmorishi@med.miyazaki-u.ac.jp.
University of Miyazaki · JPChiba Cancer Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

G protein-coupled receptor 56 (GPR56) is highly expressed in acute myeloid leukemia (AML) cells with high EVI1 expression (EVI1

Indexed as

AnimalsCell Line, TumorCell ProliferationGene Expression Regulation, LeukemicHumansImidazolesLeukemia, Myeloid, AcuteMDS1 and EVI1 Complex Locus ProteinMiceNylonsPromoter Regions, GeneticProtein BindingPyrrolesReceptors, G-Protein-CoupledXenograft Model Antitumor AssaysADGRG1 protein, humanimidazoleImidazolesMDS1 and EVI1 Complex Locus ProteinMECOM protein, humanNylonsPyrrolesReceptors, G-Protein-Coupled

Identifiers

PMID30214063
PMCPMC6137133
OpenAlexW2889737744

What OpenQuestion holds

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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.