Evidence map›Paper›PMID 30814857›Full record

ArticleTurkish journal of biology = Turk biyoloji dergisi2017

Determining expression of miRNAs that potentially regulate STAT5A and 5B in dasatinib-sensitive K562 cells.

Asu Fergün Yilmaz, Burçin Kaymaz, Çağdaş Aktan, Nur Soyer, Buket Kosova, Ajda Güneş, Fahri Şahin, Melda Cömert, Güray Saydam, Filiz Vural

Open access · bronzeAbstract read
In one paragraph

Article in Turkish journal of biology = Turk biyoloji dergisi, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 80% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

10 authors at 5 institutions in 1 country.

Asu Fergün YilmazDepartment of Hematology, İzmir Kâtip Çelebi University Atatürk Training and Research Hospital , İzmir , Turkey.
Burçin KaymazDepartment of Medical Biology, Ege University Hospital , İzmir , Turkey.
Çağdaş AktanDepartment of Medical Biology, School of Medicine, Beykent University , İstanbul , Turkey.
Nur SoyerDepartment of Hematology, Internal Medicine, Ege University Hospital , İzmir , Turkey.
Buket KosovaDepartment of Medical Biology, Ege University Hospital , İzmir , Turkey.
Ajda GüneşDepartment of Hematology, Sivas Numune Hospital , Sivas , Turkey.
Fahri ŞahinDepartment of Hematology, Internal Medicine, Ege University Hospital , İzmir , Turkey.
Melda CömertDepartment of Hematology, Internal Medicine, İnönü University Hospital , Malatya , Turkey.
Güray SaydamDepartment of Hematology, Internal Medicine, Ege University Hospital , İzmir , Turkey.
Filiz VuralDepartment of Hematology, Internal Medicine, Ege University Hospital , İzmir , Turkey.
Ege University · TRBeykent University · TRInonu University · TRIzmir Kâtip Çelebi University · TRSivas State Hospital · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the era of tyrosine kinase inhibitors, resistance still constitutes a problem in chronic myeloid leukemia (CML) patients; thus, new pathway-specific inhibitors like miRNAs have become important in the treatment of refractory patients. There are no satisfying data regarding the miRNAs and anti-miRNA treatment targeting STAT5A and 5B. In this study, we first researched the effect of dasatinib on apoptosis in the CML cell line K562. The expressions of miRNAs possibly targeting both STAT5A and 5B were then determined. The down- and upregulation of the miRNAs were compared using the ΔΔCT method. At the last stage of the study, we used a new primer probe in order to validate the results. The level of hsa-miR-940 was decreased 4.4 times and the levels of hsa-miR-527 and hsa-miR-518a-5p were increased 12.1 and 8 times, respectively, in the dasatinib-treated group when compared to the control group. We detected similar results in the validation step. As a conclusion, we determined the expression profiles of miRNAs targeting STAT5A and 5B that had an important role in the pathogenesis of CML. The data obtained could lead to determining new therapeutic targets for CML patients.

Indexed as

chronic myeloid leukemiadasatinibK562 cellsmiRNA expressionsSTAT5ASTAT5B

Identifiers

PMID30814857
PMCPMC6353289
OpenAlexW2776782596

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.