Evidence map›Paper›PMID 31025148›Full record

ArticleMolecular biology reports2019

ABL1 tyrosine kinase domain mutations in chronic myeloid leukemia treatment resistance.

Irina Cezara Vacarean-Trandafir, Iuliu Cristian Ivanov, Loredana Mihaiela Dragos, Angela Smaranda Dascalescu, Amalia Andrea Titieanu, Dumitru Cojocaru

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Article in Molecular biology reports, 2019. 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
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.

  1. Trial
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

6 authors.

Irina Cezara Vacarean-TrandafirDepartment of Molecular Genetics, Research Center Transcend, Regional Institute of Oncology, General Henri Mathias Berthelot Street, No. 2-4, 700483, Iasi, Romania. trandafirina.bi@gmail.com.ORCID http://orcid.org/0000-0002-7329-5431
Iuliu Cristian IvanovDepartment of Molecular Genetics, Research Center Transcend, Regional Institute of Oncology, General Henri Mathias Berthelot Street, No. 2-4, 700483, Iasi, Romania.
Loredana Mihaiela DragosDepartment of Molecular Genetics, Research Center Transcend, Regional Institute of Oncology, General Henri Mathias Berthelot Street, No. 2-4, 700483, Iasi, Romania.
Angela Smaranda DascalescuDepartment of Hematology, Regional Institute of Oncology, General Henri Mathias Berthelot Street, No. 2-4, 700483, Iasi, Romania.
Amalia Andrea TitieanuDepartment of Hematology, Regional Institute of Oncology, General Henri Mathias Berthelot Street, No. 2-4, 700483, Iasi, Romania.
Dumitru CojocaruDepartment of Molecular Genetics and Biochemistry, "Alexandru Ioan Cuza" University, Carol I Bd., No. 11, 700506, Iasi, Romania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of mutations in the BCR-ABL1 fusion gene transcript causes resistance to tyrosine kinase inhibitors (TKIs) based therapy in chronic myeloid leukemia (CML). Thereby, screening for BCR-ABL1 mutations is advised especially in patients undergoing poor response to treatment. In the current study the authors investigated 43 patients with CML that failed or had suboptimal response to TKIs treatment. Blood samples were collected from patients that were treated with TKIs. The analysis of genetic mutations was performed using a semi-nested PCR assay, followed by Sanger sequencing. The analysis revealed 15 mutations (32.55%): 14 point mutations and an exon 7 deletion. In roughly 30% of cases, mutations in the BCR-ABL1 fusion gene are common causes for treatment resistance.

Indexed as

AdultAgedAged, 80 and overDrug Resistance, NeoplasmFemaleFusion Proteins, bcr-ablHumansLeukemia, Myelogenous, Chronic, BCR-ABL PositiveMaleMiddle AgedMutationSequence Analysis, DNAYoung AdultFusion Proteins, bcr-ablBCR-ABL1Chronic myeloid leukemiaSanger sequencingSemi-nested PCRTyrosine kinase inhibitors

Identifiers

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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.