Evidence map›Paper›PMID 33575085›Full record

ArticleAmerican journal of cancer research2021

Degradation of BRD4 - a promising treatment approach not only for hematologic but also for solid cancer.

Karin Bauer, Anna S Berghoff, Matthias Preusser, Gerwin Heller, Christoph C Zielinski, Peter Valent, Thomas W Grunt

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 15% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
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  14. Versatile Nano-PROTAC-Induced Epigenetic Reader Degradation for Efficient Lung Cancer Therapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2022
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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

7 authors at 2 institutions in 1 country.

Karin BauerLudwig Boltzmann Institute for Hematology and Oncology, Medical University of Vienna Austria.
Anna S BerghoffDepartment of Medicine I, Division of Oncology, Medical University of Vienna Austria.
Matthias PreusserComprehensive Cancer Center, Medical University of Vienna Austria.
Gerwin HellerComprehensive Cancer Center, Medical University of Vienna Austria.
Christoph C ZielinskiComprehensive Cancer Center, Medical University of Vienna Austria.
Peter ValentLudwig Boltzmann Institute for Hematology and Oncology, Medical University of Vienna Austria.
Thomas W GruntLudwig Boltzmann Institute for Hematology and Oncology, Medical University of Vienna Austria.
Medical University of Vienna · ATComprehensive Cancer Center Vienna · AT

Funding

Austrian Science Fund FWF P 30625
6 · The paper itself

Abstract

Bromodomain (BRD) and extra-terminal (BET) proteins are epigenetic readers that regulate gene expression and promote cancer evolution. Pharmacological inactivation of BRD4 has recently been introduced as a promising anti-neoplastic approach that targets MYC oncogene expression. However, resistance against BRD4-targeting drugs has been described. We compared the efficacy of the small-molecule-type BET BRD inhibitor JQ1 with the recently developed BET protein degraders dBET1 and dBET6 in colon, breast, melanoma, ovarian, lung and prostate cancer cell lines. As determined by qPCR, all BRD4 targeting drugs dose-dependently decreased MYC expression, with dBET6 introducing the strongest downregulation of MYC. This correlated with the anti-proliferative activity of these drugs, which was at least one order of magnitude higher for dBET6 (IC

Indexed as

BET degraderdBET6MYCPD-L1solid tumor

Identifiers

PMID33575085
PMCPMC7868748
OpenAlexW3128458146

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.