Evidence map›Paper›PMID 42879015›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2027

Analysis of Regulatory DNA Sequences by Dual-Luciferase Reporter Assays in Ewing Sarcoma.

Tilman L B Hölting, Maximilian M L Knott

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2027. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Tilman L B HöltingHopp Children's Cancer Center (KiTZ), Heidelberg, Germany. tilman.hoelting@med.uni-heidelberg.de.
Maximilian M L KnottHopp Children's Cancer Center (KiTZ), Heidelberg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Reporter gene assays allow for examining the influence of regulatory DNA sequences on the transcription of target genes. In Ewing sarcoma, the study of these DNA sequences is paramount because the disease's main driver mutation is a fusion transcription factor that binds distinct motifs compared with its wild-type constituents. Here, we describe a workflow for analyzing the enhancer activity of regulatory DNA sequences using transfection-based dual-luciferase reporter assays in Ewing sarcoma cell lines. To this end, we provide a protocol for cloning genomic sequences into a firefly luciferase-containing plasmid, co-transfecting Ewing sarcoma cells with firefly reporter and Renilla control plasmids and measuring luciferase expression by luminescence. The entire procedure can be completed in 14 days.

Indexed as

Genes, ReporterRegulatory Sequences, Nucleic AcidSarcoma, EwingCell Line, TumorEnhancer Elements, GeneticGene Expression Regulation, NeoplasticHumansLuciferases, FireflyPlasmidsPromoter Regions, GeneticTransfectionLuciferases, FireflyEnhancer activityFusion-driven sarcomaGene expressionLuciferase assayPromoter activityRegulatory DNARegulatory sequencesReporter assays

Identifiers

PMID42879015

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.