Investigating how SIN3a affects a key receptor in pulmonary arterial hypertension

Who could benefit from this research

What this research studies

This research focuses on understanding the role of SIN3a in regulating the Bone Morphogenetic Protein Receptor Type 2 (BMPR2), which is crucial for maintaining healthy blood vessels in the lungs. By exploring the molecular mechanisms that lead to changes in BMPR2 expression, the study aims to uncover how these changes contribute to pulmonary arterial hypertension (PAH), a serious condition characterized by high blood pressure in the lungs. The research involves examining the epigenetic modifications that affect BMPR2 in pulmonary artery endothelial cells, which may provide insights into potential therapeutic targets for PAH. Patients may benefit from a better understanding of the disease mechanisms, potentially leading to new treatment strategies.

Why it matters

Where this research is happening

• New York Medical College
  Valhalla, United States Active

Researchers

• Principal investigator: Bisserier, Malik — New York Medical College
• Study coordinator: Bisserier, Malik

Related research

Other NIH-funded projects on the same topics.

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• Asporin as a double-targeted therapy and biomarker for a serious artery disease

  This project tests a protein called asporin as both a treatment and a biomarker for pulmonary arterial hypertension (PAH) to help people with this life-threatening condition.

  NIH research University of California Los Angeles · Los Angeles, United States · NIH-11450594

• Platelets and fibroblasts linked to energy use in a hard-to-treat blood vessel disease

  A research team at the University of Pittsburgh is studying how platelet energy metabolism and fibroblast glutamine use interact in systemic sclerosis-related pulmonary arterial hypertension to improve diagnosis and treatment.

  NIH research University of Pittsburgh at Pittsburgh · Pittsburgh, United States · NIH-11419895

• A biatrial dual‑lumen catheter to help the heart and lungs in pulmonary arterial hypertension

  A new double‑lumen catheter is being developed to unload the right side of the heart and protect the lungs for people with pulmonary arterial hypertension.

  NIH research Icahn School of Medicine at Mount Sinai · New York, United States · NIH-11418121

• Endothelial inflammation and Src kinase in early pulmonary arterial hypertension

  Researchers are studying how inflammation in the lining of blood vessels and a protein called Src kinase contribute to early lung artery remodeling in people with mild PAH.

  NIH research Brigham and Women's Hospital · Boston, United States · NIH-11411210

• Cardiopulmonary chip model to study right heart disease from high blood pressure in the lungs

  A tiny heart-lung chip is being developed to understand why the right side of the heart enlarges in people with pulmonary arterial hypertension and to test targeted treatments.

  NIH research Medluidics LLC · Elk Grove, United States · NIH-11410451

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.