Evidence map›Paper›PMID 33255664›Full record

ArticleInternational journal of molecular sciences2020

Microfluidic-Based Detection of AML-Specific Biomarkers Using the Example of Promyelocyte Leukemia.

Benedikt Emde, Heike Kreher, Nicole Bäumer, Sebastian Bäumer, Dominique Bouwes, Lara Tickenbrock

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 45% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
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  5. 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

6 authors at 2 institutions in 1 country.

Benedikt EmdeDepartment Hamm 1, Hamm-Lippstadt University of Applied Science, 59063 Hamm, Germany.
Heike KreherMicronit GmbH, 44263 Dortmund, Germany.
Nicole BäumerDepartment of Medicine A, Hematology and Oncology, University of Muenster, 48149 Muenster, Germany.
Sebastian BäumerDepartment of Medicine A, Hematology and Oncology, University of Muenster, 48149 Muenster, Germany.
Dominique BouwesMicronit GmbH, 44263 Dortmund, Germany.
Lara TickenbrockDepartment Hamm 1, Hamm-Lippstadt University of Applied Science, 59063 Hamm, Germany.
Hamm-Lippstadt University of Applied Sciences · DEUniversity of Münster · DE

Funding

Research funded by "Zentrales Innovationsprogramm Mittelstand (ZIM)" by the "Bundesministerium für Wirtschaft und Energie" ZF4147102SB6
6 · The paper itself

Abstract

A microfluidic assay for the detection of promyelocytic leukemia (PML)-retinoic acid receptor α (RARα) fusion protein was developed. This microfluidic-based system can be used for rapid personalized differential diagnosis of acute promyelocyte leukemia (APL) with the aim of early initiation of individualized therapy. The fusion protein PML-RARα occurs in 95% of acute promyelocytic leukemia cases and is considered as diagnostically relevant. The fusion protein is formed as a result of translocation t(15,17) and is detected in the laboratory by fluorescence in situ hybridization (FISH) or reverse transcriptase polymerase chain reaction (RT-PCR). Diagnostic methods require many laboratory steps with specialized staff. The developed microfluidic assay includes a sandwich enzyme-linked immunosorbent assay (ELISA) system for PML-RARα on surface of magnetic microparticles in a microfluidic chip. A rapid detection of PML-RARα in cell lysates is achieved in less than one hour. A biotinylated PML-antibody on the surface of magnetic streptavidin coated microparticles is used as capture antibody. The bound translocation product is detected by a RARα antibody conjugated with horseradish peroxidase and the substrate QuantaRed. The analysis is performed in microfluidic channels which involves automated liquid processing with stringent washing and short incubation times. The results of the developed assay show that cell lysates of PML-RARα-positive cells (NB-4) can be clearly distinguished from PML-RARα-negative cells (HL-60, MV4-11).

Indexed as

Biomarkers, TumorGranulocyte Precursor CellsHumansIn Situ Hybridization, FluorescenceLeukemia, Promyelocytic, AcuteMicrofluidicsOncogene Proteins, FusionPrecision MedicinePromyelocytic Leukemia ProteinRetinoic Acid Receptor alphaTranslocation, GeneticBiomarkers, TumorOncogene Proteins, FusionPML protein, humanPromyelocytic Leukemia Proteinpromyelocytic leukemia-retinoic acid receptor alpha fusion oncoproteinRARA protein, humanRetinoic Acid Receptor alphaacute myeloid leukemiabio-microfluidicslab-on-a-chipmagnetic bead-based immunoassaypersonalized diagnostics and medicine

Identifiers

PMID33255664
PMCPMC7728129
OpenAlexW3109759089

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.