Understanding how a protein complex affects gene silencing related to sickle cell disease

The role of the MBD2-NuRD complex in gamma-globin gene silencing

NIH-funded research Virginia Commonwealth University · NIH-10442549

This study is looking at a special protein complex that helps control blood gene activity, with the hope of finding new ways to boost healthy hemoglobin levels in adults with sickle cell disease and beta-thalassemia, ultimately aiming to create safer treatments for these conditions.

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionVirginia Commonwealth University NIH-funded
Lab location1 site (Richmond, United States)
Project IDNIH-10442549 on NIH RePORTER

What this research studies

This research investigates the MBD2-NuRD complex, which plays a crucial role in regulating the expression of globin genes, particularly in the context of sickle cell disease and beta-thalassemia. By examining how this protein complex interacts with specific genes, the researchers aim to identify potential therapeutic targets that could activate fetal hemoglobin expression in adults. The study employs advanced techniques such as genome editing and structural analysis to explore these interactions in adult human erythroid cells. The ultimate goal is to develop safe therapies that could improve outcomes for patients with these blood disorders.

Who could benefit from this research

Good fit: Ideal candidates for this research are adults diagnosed with sickle cell disease or beta-thalassemia.

Not a fit: Patients with other forms of anemia or blood disorders unrelated to sickle cell disease or beta-thalassemia may not benefit from this research.

Why it matters

Potential benefit: If successful, this research could lead to new treatments that increase fetal hemoglobin levels in patients with sickle cell disease and beta-thalassemia, potentially alleviating symptoms and complications.

How similar studies have performed: Previous research has shown promise in targeting similar epigenetic mechanisms to treat blood disorders, indicating that this approach could be viable.

Where this research is happening

Richmond, United States

Researchers

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page below.
Conditions Hb SS diseaseHbSS diseaseHemoglobin S DiseaseHemoglobin sickle cell diseaseHemoglobin sickle cell disorder
Last reviewed 2026-06-13 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.