Evidence map›Paper›PMID 35485671›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2022

Hsa-miR-625 Upregulation Promotes Apoptosis in Acute Myeloid Leukemia Cell Line by Targeting Integrin-linked Kinase Pathway.

Bahareh Aliabedi, Seyed Hadi Mousavi, Marzieh Ebrahimi, Shaban Alizadeh, Amir Abbas Hedayati Asl, Monireh Mohammad, Sahar Samieyan Dehkordi

Open access · greenAbstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 52% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
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  3. Review
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

7 authors at 2 institutions in 1 country.

Bahareh AliabediDepartment of Hematology, School of Allied Medical Sciences, Tehran University of Medical Sciences, Tehran, Iran.
Seyed Hadi MousaviDepartment of Hematology, School of Allied Medical Sciences, Tehran University of Medical Sciences, Tehran, Iran.ORCID 0000-0002-0163-5839
Marzieh EbrahimiDepartment of Regenerative Biomedicine, Cell Science Research Center, Royan Institute for Stem Cell Biology & Technology, ACECR, Tehran, Iran.
Shaban AlizadehDepartment of Hematology, School of Allied Medical Sciences, Tehran University of Medical Sciences, Tehran, Iran.
Amir Abbas Hedayati AslDepartment of Regenerative Biomedicine, Cell Science Research Center, Royan Institute for Stem Cell Biology & Technology, ACECR, Tehran, Iran.
Monireh MohammadDepartment of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology & Technology, ACECR, Tehran, Iran.
Sahar Samieyan DehkordiDepartment of Hematology, School of Allied Medical Sciences, Tehran University of Medical Sciences, Tehran, Iran.
Tehran University of Medical Sciences · IRRoyan Institute · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGrowing evidence has demonstrated that microRNAs have a major effect on development of different types of cancer including AML. The overexpression of miR-625 could decrease tumorgenesis of acute myeloid leukemia cell lines through Integrin-linked kinase signaling pathway and reducing the associated oncogenes.  The aim of this study is to evaluate the effect of hsa-miR-625 upregulation on apoptosis and proliferation of KG1 cell line via ILK signaling pathway.

methodsThe KG-1 cell line was transfected with pLenti-III-premir625-GFP through viral method. Then, expression of miR-625 and genes were analyzed by quantitative PCR. Western blotting was used to evaluate for the protein level. Apoptosis was investigated by flow cytometry. Cell cycle analysis with PI and CCK-8 assay were performed to evaluate proliferation.

resultsKG-1 cells transfected with pLenti-III-pre mir625-GFP construct showed a significant increase in cell apoptosis. Gene expression of ILK and NF-κB were downregulated and AKT, c-fos, Caspase3, cyclin D1, KLF-4, OCT-4 and Nanog were upregulated but no alteration in GSK3 expression profile was observed. Downregulation of NF-κB and upregulation of Caspase 3 and p-β-catenin protein levels were indicated (p<0.05).

conclusionMiR-625 can be a promising approach to aid in the treatment of AML. However, further studies are required in this respect.

Indexed as

Leukemia, Myeloid, AcuteMicroRNAsApoptosisCell Line, TumorCell ProliferationGlycogen Synthase Kinase 3HumansNF-kappa BProtein Serine-Threonine KinasesScaffold Protein ILKUp-RegulationGlycogen Synthase Kinase 3MicroRNAsMIRN625 microRNA, humanNF-kappa BProtein Serine-Threonine KinasesScaffold Protein ILKAMLApoptosisKG-1miR-625Proliferation

Identifiers

PMID35485671
PMCPMC9375600
OpenAlexW4225125641

What OpenQuestion holds

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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.