Evidence map›Paper›PMID 42573695›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Reporter Gene Assay for Monitoring BCL6 Reactivation.

Catherine L Ingram, Radosław P Nowak, Thomas M Geiger

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2026. 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

3 authors.

Catherine L IngramInstitute of Structural Biology, University of Bonn, Bonn, Germany.
Radosław P NowakInstitute of Structural Biology, University of Bonn, Bonn, Germany. radoslaw.nowak@uni-bonn.de.
Thomas M GeigerInstitute of Structural Biology, University of Bonn, Bonn, Germany. tgeiger@uni-bonn.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transcription factors are an exciting class of drug targets. Recent developments in small molecule-induced proximity allow for small molecule control of their activity by recruitment of epigenetic proteins. In this chapter, we describe the development of a transcriptional activity assay for the transcription factor BCL6 with a small molecule activator, TCIP1, in HEK293T cells [1]. The assay is based on the Bio-Glo Luciferase assay system and uses transient transfection of a BCL6-expressing plasmid, as well as a reporter plasmid where a BCL6 DNA-binding sequence controls expression of a luciferase protein. The method described here is specific to BCL6 but can easily be optimized to monitor the activity of other transcription factors by altering the DNA-binding sequence of the reporter.

Indexed as

Genes, ReporterProto-Oncogene Proteins c-bcl-6Transcriptional ActivationHEK293 CellsHumansLuciferasesPlasmidsTransfectionBCL6 protein, humanLuciferasesProto-Oncogene Proteins c-bcl-6BCL6Induced proximityReporter gene assayTCIPTranscription activation

Identifiers

PMID42573695

What OpenQuestion holds

Textmetadata
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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.