NIH-funded research R01 grant

RUNX3 and changes in artery walls

Official title: RUNX3 in Vascular Wall Remodeling

Funded at University of Texas Hlth Ctr at Tyler · NIH-11258536 · Data updated 2026-11-12

This project looks at whether changing the RUNX3 protein can stop artery wall cells from turning into an overgrown, disease-causing state in adults with artery disease or after angioplasty.

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionUniversity of Texas Hlth Ctr at Tyler
NIH-funded
Lab location1 site (Tyler, United States)
Project startJanuary 5, 2024
Project endDecember 31, 2028
Funding year2026
Award (this year)$425,215
NIH project number5R01HL166906-03
Project IDNIH-11258536 on NIH RePORTER

Who could benefit from this research

Could help

Adults with atherosclerosis, coronary artery disease, hypertension, aneurysm, or patients who have had or will have angioplasty would be the most relevant candidates to contribute samples or be considered for future trials.

Less likely to help

People without vascular disease, children, or those whose conditions are not driven by smooth muscle cell remodeling are unlikely to benefit directly from this work in the near term.

What this research studies

Researchers will change RUNX3 levels in vascular smooth muscle cells in the lab and expose those cells to growth signals like PDGF-BB to see how they respond. They will measure contractile markers, cell proliferation, and signaling molecules such as myocardin/SRF and c-Myc to understand how RUNX3 controls the cell switch. The team will use cell-based experiments and may use animal models to study how RUNX3 affects artery wall remodeling. Results will be used to guide future ways to prevent restenosis after angioplasty or slow atherosclerosis progression.

Why it matters

Potential benefit: If successful, this work could point to new treatments that prevent artery narrowing and complications after angioplasty by targeting RUNX3-driven changes.

How similar studies have gone: Laboratory studies have long shown that PDGF-BB drives smooth muscle cell changes and the investigators' preliminary data link RUNX3 to that process, but targeting RUNX3 as a therapy is novel and has not yet been tested in patients.

Where this research is happening

  • University of Texas Hlth Ctr at Tyler
    Tyler, United States
    Active

Researchers

  • Principal investigator: Guo, Xia — University of Texas Hlth Ctr at Tyler
  • Study coordinator: Guo, Xia

Related research

Other NIH-funded projects on the same topics.

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.
Last reviewed 2026-11-14 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.