NIH-funded research R01 grant

Understanding how RNA binding proteins drive liver scarring and how to slow it down

Official title: Post-transcriptional regulation by RNA binding proteins in liver fibrosis

Funded at Sanford Burnham Prebys Medical Discovery Institute · NIH-11449893 · Data updated 2026-11-12

A researcher team is studying how certain RNA binding proteins, especially LARP6, regulate the liver’s scar-building process in alcoholic liver disease to identify potential ways to reduce fibrosis.

More Fibrosis research and trials

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionSanford Burnham Prebys Medical Discovery Institute
NIH-funded
Lab location1 site (La Jolla, United States)
Project startAugust 10, 2026
Project endApril 30, 2030
Funding year2026
Award (this year)$910,940
NIH project number1R01DK145938-01A1
Project IDNIH-11449893 on NIH RePORTER

Who could benefit from this research

Could help

Patients with alcoholic liver disease or MASLD/MetALD who are at risk of fibrosis and may benefit from future anti-fibrotic therapies.

Less likely to help

This grant is primarily a basic science study; it does not involve direct patient treatment, and immediate benefits to individuals are not guaranteed.

What this research studies

Chronic liver injury from alcohol and related conditions can cause fibrosis, the buildup of scar tissue that can lead to cirrhosis and liver failure. This project looks at the tiny molecular players called RNA binding proteins that control how scar proteins like collagen are made in liver cells. By focusing on LARP6 and other RBPs, researchers will map which proteins influence fibrosis and how they interact with RNA and other cellular partners. The goal is to uncover targets for therapies that could dampen fibrotic processes before permanent damage occurs in patients with MASLD/MetALD-related liver disease.

Why it matters

Potential benefit: If successful, the work could point to new therapeutic strategies to reduce liver fibrosis and improve outcomes for people with alcoholic liver disease and related conditions.

How similar studies have gone: Previous studies in other organs suggest RBPs influence fibrotic processes, supporting potential relevance to liver disease, though liver-specific evidence is ongoing.

Where this research is happening

  • Sanford Burnham Prebys Medical Discovery Institute
    La Jolla, United States
    Active

Researchers

  • Principal investigator: Brenner, David a. — Sanford Burnham Prebys Medical Discovery Institute
  • Study coordinator: Brenner, David a.

Related research

Other NIH-funded projects on the same topics.

  • Role of SMAD1/5/8 signaling in liver fibrosis

    This grant explores how specific liver cell signals influence scarring (fibrosis) in the liver, with a focus on people who have alcohol-related liver disease or related conditions.

    NIH research University of Arizona · Tucson, United States · NIH-11504353

  • Targeting TGF-βRII to treat alcoholic liver fibrosis

    A study to test a new peptide that blocks a key fibrosis signal and a gene-silencing approach to help reverse liver fibrosis caused by alcohol use.

    NIH research University of Missouri Kansas City · Kansas City, United States · NIH-11466092

  • S100A9+ immune cells driving liver scarring in MASLD/MASH

    Affects people with MASLD/MASH may benefit from a better understanding of how certain immune cells contribute to liver fibrosis and how to stop it.

    NIH research Massachusetts General Hospital · Boston, United States · NIH-11429726

  • Liver fibrosis test platform using patient-derived liver tissue to speed anti-fibrosis drugs

    A patient-focused liver fibrosis test platform is being developed to help speed the creation of medicines that treat liver scarring by using human-derived liver cells and tissue signals.

    NIH research Xylyx Bio, INC. · Brooklyn, United States · NIH-11413845

  • Role of HK2 in liver scarring, fatty liver disease, and liver cancer

    A study in adults looks at how the enzyme HK2 helps drive liver scarring in NASH and may influence the development of liver cancer, with potential to point to new treatments.

    NIH research University of Illinois at Chicago · Chicago, UNITED STATES · NIH-11400510

  • Novel Paxillin-FAK Inhibitors for Liver Fibrosis

    A new program is testing Paxillin-FAK inhibitors to slow or stop liver fibrosis in adults with liver diseases like alcoholic liver disease and MASH.

    NIH research Faknostics, LLC · Phoenix, United States · NIH-11387961

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.