NIH-funded research NIH-funded research

Using genetic discoveries to improve outcomes for high-risk acute leukemia

Official title: Translating genomic discoveries to improved outcomes for high risk acute leukemia

Funded at St. Jude Children's Research Hospital · NIH-11210476 · Data updated 2026-11-12

Researchers are using genetic information from people with high-risk acute leukemia to find why the cancer starts and why some treatments fail so they can create better tests and targeted therapies.

More Acute Leukemia research and trials

Quick facts

Grant typeNIH-funded research
Study typeNIH-funded research
Funding institutionSt. Jude Children's Research Hospital
NIH-funded
Lab location1 site (Memphis, United States)
Project startJanuary 19, 2017
Project endAugust 31, 2030
Funding year2025
Award (this year)$12,654
NIH project number3R35CA197695-10S1
Project IDNIH-11210476 on NIH RePORTER

Who could benefit from this research

Could help

People with high‑risk or treatment‑resistant acute leukemia, including children and adults whose cancer carries the specific genetic changes under study, would be the most relevant candidates.

Less likely to help

Patients with low‑risk leukemia types not related to the genetic alterations studied, or individuals without acute leukemia, are unlikely to see direct benefit from this program.

What this research studies

This program analyzes the genomes of leukemia samples and uses lab models to find the genetic changes that drive aggressive or treatment‑resistant disease. Scientists study how those changes alter gene control, chromatin structure, and cell behavior, including a process called liquid‑liquid phase separation. The team is testing new approaches such as targeted protein degradation aimed at cancer drivers that have been hard to treat. Work builds on previously identified leukemia subtypes and uses patient samples alongside experimental systems to move findings toward new diagnostics and therapies.

Why it matters

Potential benefit: If successful, this work could produce new tests and targeted treatments that improve cure rates for children and others with high‑risk acute leukemia.

How similar studies have gone: Previous genomic studies and the team's own work have already reclassified leukemia subtypes and shown promising early results with targeted approaches, providing a strong foundation for this program.

Where this research is happening

  • St. Jude Children's Research Hospital
    Memphis, United States
    Active

Researchers

  • Principal investigator: Mullighan, Charles G — St. Jude Children's Research Hospital
  • Study coordinator: Mullighan, Charles G

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.