Target intelligence / Profile preview

Mediator complex subunit 24 (MED24)

Target
MED24
Molecular classification
Transcription factor (Mediator complex subunit), Nuclear receptor-associated coactivator, Tail module component of the Mediator complex
01

Overview

Mediator complex subunit 24 (MED24) is a component of the multi-protein Mediator complex, which enables the transcription of protein-coding genes by bridging regulatory elements and the RNA polymerase II enzyme. MED24 is classified as part of the "tail" module of the complex, and is essential for integration of cell signaling pathways (such as FGF/ERK) and nuclear receptor signaling (e.g. estrogen receptor, vitamin D receptor) in embryonic stem cells and other cell types. Loss of MED24 disrupts differentiation and cell fate decisions by impairing the transcriptional response to signaling cues. MED24 is highly conserved across eukaryotes and functions as a coactivator in a range of tissues and developmental processes. It is implicated in cancer and developmental disorders associated with abnormal gene regulation.

Other names
ARC100CRSP4DRIP100KIAA0130THRAP4TRAP100CRSP complex subunit 4Trap100hTRAP100CRSP100MED5Activator-recruited cofactor 100 kDa componentCofactor required for Sp1 transcriptional activation subunit 4Thyroid hormone receptor-associated protein 4Vitamin D3 receptor-interacting protein complex 100 kDa component
02

Mechanism of action

Drugs (e.g. hormone analogs) acting upstream on nuclear receptors can modulate the gene expression by influencing Mediator complex recruitment, including MED24’s involvement.

03

Biological functions

Transcriptional regulation by RNA polymerase IIMediator of enhancer-promoter communicationSignal transduction (links FGF/ERK signaling to nuclear receptor engagement in stem cells)Regulation of cell differentiation, particularly primitive endoderm formation in embryonic stem cells
04

Disease associations

Cancer (implicated via Mediator complex in transcriptional misregulation)Developmental diseases (linked to defective differentiation in stem cell models)Other (potential roles in neurodevelopment and hormone response via nuclear receptor interaction)
05

Safety considerations

Targeting core transcription machinery, such as Mediator subunits, may pose risks of broad transcriptional dysregulation, leading to potential cytotoxicity or off-target gene expression effects
06

Interacting drugs

Drugs acting on nuclear hormone receptors (such as estrogen, thyroid hormone, and vitamin D3 analogs) may indirectly impact MED24-mediated transcriptional regulation, but no drugs directly targeting MED24 are described in the search results
07

Biomarkers

MED24 expression may serve as a biomarker of cell pluripotency and differentiation status in stem cell applications

Beyond the preview

Go deeper on Mediator complex subunit 24 (MED24).

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Drug pipeline

Full profile access

Explore the programs pursuing this target and their development progress.

  • Drug candidates
  • Developers
  • Development stage

Clinical trials

Full profile access

Follow the clinical studies evaluating therapies directed at this target.

  • Trial design
  • Status
  • Readouts

Competitive landscape

Full profile access

Compare approaches across drug candidates, modalities, and indications.

  • Programs
  • Modalities
  • Indications

Literature & evidence

Full profile access

Investigate the research and source evidence behind target biology and development.

  • Publications
  • Sources
  • Analysis

Patents

Full profile access

Explore patent activity around therapies and technologies addressing this target.

  • Patents
  • Assignees
  • Technologies

Research & analysis

Full profile access

Connect target biology, drug development, and emerging evidence in your research.

  • Biology
  • Development news
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on Mediator complex subunit 24 (MED24).

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call