Evidence map›Paper›PMID 40565048›Full record

ArticleInternational journal of molecular sciences2025

Improvement in Transient Agarose Spot (TAS) Cell Migration Assay: Microplate-Based Detection and Evaluation.

Apor Veres-Székely, Csenge Szász, Domonkos Pap, Péter Bokrossy, Dorina Lenzinger, Tamás Visnovitz, Judith Mihály, Marcell Pálmai, Zoltán Varga, László Őrfi and 3 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. 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. Anti-fibrotic effect ofFrontiers in bioengineering and biotechnology · 2026
    Article
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

13 authors.

Apor Veres-SzékelyPediatric Center, Semmelweis University, 1083 Budapest, Hungary.ORCID 0000-0002-6830-8779
Csenge SzászPediatric Center, Semmelweis University, 1083 Budapest, Hungary.
Domonkos PapPediatric Center, Semmelweis University, 1083 Budapest, Hungary.
Péter BokrossyPediatric Center, Semmelweis University, 1083 Budapest, Hungary.
Dorina LenzingerInstitute of Genetics, Cell and Immunobiology, Semmelweis University, 1089 Budapest, Hungary.ORCID 0000-0003-0270-7985
Tamás VisnovitzInstitute of Genetics, Cell and Immunobiology, Semmelweis University, 1089 Budapest, Hungary.
Judith MihályTTK Biological Nanochemistry Research Group, Institute of Materials and Environmental Chemistry, Research Centre for Natural Sciences, 1117 Budapest, Hungary.
Marcell PálmaiTTK Biological Nanochemistry Research Group, Institute of Materials and Environmental Chemistry, Research Centre for Natural Sciences, 1117 Budapest, Hungary.ORCID 0000-0001-9348-0733
Zoltán VargaTTK Biological Nanochemistry Research Group, Institute of Materials and Environmental Chemistry, Research Centre for Natural Sciences, 1117 Budapest, Hungary.
László ŐrfiVichem Chemie Research Ltd., 1022 Budapest, Hungary.
Attila J SzabóPediatric Center, Semmelweis University, 1083 Budapest, Hungary.
Ádám VannayPediatric Center, Semmelweis University, 1083 Budapest, Hungary.
Beáta SzebeniPediatric Center, Semmelweis University, 1083 Budapest, Hungary.

Funding

National Research, Development and Innovation Office EKÖP-2024-160National Research, Development and Innovation Office EKÖP-2024-162National Research, Development and Innovation Office EKÖP-2024-53National Research, Development and Innovation Office K-142728National Research, Development and Innovation Office RRF-2.3.121-2022-00003National Research, Development and Innovation Office TKP2021-EGA-23National Research, Development and Innovation Office TKP2021-EGA-24National Research, Development and Innovation Office VEKOP-2.3.3-15-2017-00016
6 · The paper itself

Abstract

Collective cell migration is crucial in various biological processes, including tumor progression and metastasis. The widely used scratch assay (wound healing assay) has limitations in throughput, reproducibility, and data analysis. To overcome these challenges, we previously developed the Transient Agarose Spot (TAS) assay, which enhanced assay precision and reproducibility. In this study, we present an improved microplate-based TAS assay. By using a microplate reader, we automated data acquisition, enabling the detection of cell migration in a 96-well plate format with greater throughput and accuracy. The new method applies Hoechst staining to label viable cells, providing a stable signal for kinetic analysis without compromising cell viability. We validated this approach with fluorophore-expressing cancer cells and demonstrated its ability to monitor dose-dependent effects of fetal bovine serum on cell migration. Additionally, we applied the microplate-based TAS assay to assess the anti-migratory effects of kinase inhibitors and mesenchymal stem cell-derived extracellular vesicles (EVs) on lung cancer cells. The assay accurately quantified migration inhibition and revealed the concentration-dependent effects of EVs, highlighting their potential as therapeutic agents. This microplate-based TAS assay provides a scalable, efficient, and cost-effective platform for high-throughput screening of cell migration and drug discovery, offering a robust alternative to traditional microscopy-based methods.

Indexed as

Cell Migration AssaysCell MovementSepharoseCell Line, TumorCell SurvivalExtracellular VesiclesHigh-Throughput Screening AssaysHumansMesenchymal Stem CellsProtein Kinase InhibitorsReproducibility of ResultsProtein Kinase InhibitorsSepharosecell migrationHoechstmicroplate readerTAS assay

Identifiers

PMID40565048
PMCPMC12192967

What OpenQuestion holds

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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.