Eyes Toward the Clinic: Selective Inhibition and Degradation Approaches to Bromodomain‐Containing Proteins

Bromodomain-containing proteins serve as epigenetic regulators, where bromodomains recognize acetylated proteins and histones to drive changes in gene expression. Due to their regulatory role in gene expression, bromodomain-containing proteins have served as important targets for drug-discovery efforts, in particular the bromodomain and extra-terminal (BET) family proteins. The selective targeting of these proteins through both inhibition and targeted protein degradation has revealed diverse biological mechanisms. For BET bromodomain-containing proteins, we discuss the unique biological effects of selective inhibition and degradation for efficacy and clinical safety concerns for both BET inhibitors that have entered Phase III clinical trials and recent BET degrader clinical candidates. We also describe the current inhibitory and targeted protein degradation approaches of non-BET bromodomain-containing proteins. This review summarizes current approaches of bromodomain-targeting inhibition and degradation to provide insight on molecular mechanisms and updates the clinical progress of these modalities as the field awaits the approval of the first bromodomain-targeted therapeutic.

Authors

Institutions

Publication Details

Journal
ChemBioChem
Published
2026-06-30
DOI
https://doi.org/10.1002/cbic.70443
Primary Topic
Protein Degradation and Inhibitors
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Eyes Toward the Clinic: Selective Inhibition and Degradation Approaches to Bromodomain‐Containing Proteins

William C. K. Pomerantz, Cole R. Scholtz
ChemBioChem
Protein Degradation and Inhibitors
article

Eyes Toward the Clinic: Selective Inhibition and Degradation Approaches to Bromodomain‐Containing Proteins

William C. K. Pomerantz, Cole R. Scholtz
article en

Abstract

Bromodomain-containing proteins serve as epigenetic regulators, where bromodomains recognize acetylated proteins and histones to drive changes in gene expression. Due to their regulatory role in gene expression, bromodomain-containing proteins have served as important targets for drug-discovery efforts, in particular the bromodomain and extra-terminal (BET) family proteins. The selective targeting of these proteins through both inhibition and targeted protein degradation has revealed diverse biological mechanisms. For BET bromodomain-containing proteins, we discuss the unique biological effects of selective inhibition and degradation for efficacy and clinical safety concerns for both BET inhibitors that have entered Phase III clinical trials and recent BET degrader clinical candidates. We also describe the current inhibitory and targeted protein degradation approaches of non-BET bromodomain-containing proteins. This review summarizes current approaches of bromodomain-targeting inhibition and degradation to provide insight on molecular mechanisms and updates the clinical progress of these modalities as the field awaits the approval of the first bromodomain-targeted therapeutic.

ChemBioChemVol. 27(13)
University of Minnesota (US), University of Minnesota System (US), Twin Cities Orthopedics (US)
National Institute of General Medical Sciences
Good health and well-being
Openalex Percentile: Top 11%
Protein Degradation and Inhibitors
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.