NIH-funded research NIH-funded research

Refolding Mutant p53: A Strategy to Help People with Li-Fraumeni Syndrome

Official title: Refolding Mutant p53: A Strategy for Cancer Prevention in Li-Fraumeni Syndrome

Funded at Research Inst of Fox Chase Can Ctr · NIH-11415067 · Data updated 2026-11-12

Aims to develop drugs that stabilize mutant p53 in people with Li-Fraumeni syndrome to prevent cancers before they develop.

More Li-Fraumeni Syndrome research and trials

Quick facts

Grant typeNIH-funded research
Study typeNIH-funded research
Funding institutionResearch Inst of Fox Chase Can Ctr
NIH-funded
Lab location1 site (Philadelphia, United States)
Project startSeptember 1, 2022
Project endAugust 31, 2027
Funding year2026
Award (this year)$378,410
NIH project number5U54CA272686-05
Project IDNIH-11415067 on NIH RePORTER

Who could benefit from this research

Could help

Individuals with Li-Fraumeni syndrome or germline TP53 mutations who are at high risk of developing cancer might benefit in the future.

Less likely to help

People without Li-Fraumeni syndrome or TP53-related cancer risk are unlikely to benefit.

What this research studies

This project targets Li-Fraumeni syndrome, an inherited cancer-prone condition caused by TP53 mutations. Researchers are testing drugs that stabilize misfolded p53 so it can regain its cancer-fighting function before tumors form. The approach uses cancer cell lines and biochemical studies to understand how these drugs fix p53’s structure and activity. If successful, this could lead to prevention strategies for individuals at high risk due to TP53 mutations.

Why it matters

Potential benefit: If successful, the work could lead to a preventive therapy that reduces cancer risk for people with Li-Fraumeni syndrome.

How similar studies have gone: Previous efforts show that stabilizing p53 can influence cancer-related processes, but translating this to prevention in LFS is still under exploration.

Where this research is happening

  • Research Inst of Fox Chase Can Ctr
    Philadelphia, United States
    Active

Researchers

  • Principal investigator: Golemis, Erica a. — Research Inst of Fox Chase Can Ctr
  • Study coordinator: Golemis, Erica a.

Related research

Other NIH-funded projects on the same topics.

  • Cancer screening with cell-free DNA in Li-Fraumeni Syndrome

    A new, patient-friendly screening approach using blood tests to look for cancer signals in people with Li-Fraumeni Syndrome, alongside standard imaging.

    NIH research Children's Hosp of Philadelphia · Philadelphia, United States · NIH-11291983

  • Reversing mutations in a protein linked to cancer risk

    This study is exploring a new way to help people with certain genetic mutations that affect the VHL protein, which can increase cancer risk, by developing compounds that might help the protein work better and reduce the chances of cancer.

    NIH research Research Inst of Fox Chase Can Ctr · Philadelphia, United States · NIH-11174990

  • Helping mutated p53 fold correctly to lower cancer risk in Li‑Fraumeni syndrome

    This project tests drugs that help mutated p53 protein fold properly to lower cancer risk for people with Li‑Fraumeni syndrome.

    NIH research Research Inst of Fox Chase Can Ctr · Philadelphia, United States · NIH-11168825

  • Improving cancer prevention for people with Li-Fraumeni syndrome

    This study is looking at how to create new medications that can help people with Li-Fraumeni syndrome by fixing a faulty protein linked to cancer, with the goal of preventing tumors from developing.

    NIH research Research Inst of Fox Chase Can Ctr · Philadelphia, United States · NIH-10909964

  • Using video capsules to examine patients with Lynch Syndrome

    This study is testing whether video capsules can be a good alternative to regular colonoscopies for people with Lynch Syndrome to help improve cancer screening.

    Recruiting Royal Marsden NHS Foundation Trust · London, (Select) · NCT06712095

  • Understanding genetic causes of neuroendocrine tumors in Mexican patients

    This study is trying to find out the genetic changes that cause neuroendocrine tumors in Mexican patients to help develop better treatments.

    Recruiting at 3 sites Universidad Nacional Autonoma de Mexico · Mexico City, Mexico City and 2 other locations · NCT06523582

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.