NIH-funded research R01 grant

Targeting epigenetic changes in IDH‑mutant, ATRX‑loss adult astrocytoma

Official title: Targeting oncogenic epigenetic mechanisms in IDHmut/ATRXloss Astrocytoma

Funded at Hugo W. Moser Res Inst Kennedy Krieger · NIH-11290314 · Data updated 2026-11-12

Researchers are working to help the immune system better recognize and attack adult astrocytoma tumors that have IDH mutations and ATRX loss.

More Astrocytoma research and trials

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionHugo W. Moser Res Inst Kennedy Krieger
NIH-funded
Lab location1 site (Baltimore, United States)
Project startMarch 1, 2024
Project endFebruary 28, 2029
Funding year2026
Award (this year)$339,878
NIH project number5R01NS135208-03
Project IDNIH-11290314 on NIH RePORTER

Who could benefit from this research

Could help

Adults with lower‑grade (WHO II/III) astrocytoma carrying IDH mutations and ATRX loss (often with p53 mutations) would be the most relevant patient group for this work.

Less likely to help

Patients without the IDH‑mutant/ATRX‑loss molecular profile, pediatric patients, or those with unrelated brain tumor types are unlikely to directly benefit from these specific findings.

What this research studies

From a patient perspective, the team will study why adult IDH‑mutant/ATRX‑loss astrocytoma cells hide from the immune system by examining tumor tissue, 3‑D lab models, and related preclinical models. They will look at how these tumor cells lower antigen presentation, become less responsive to interferon‑gamma signals, and up‑regulate checkpoint molecules that block immune attack. Using those findings, the researchers plan to test laboratory strategies to restore antigen presentation and immune sensitivity and to combine those strategies with emerging immunotherapies. The goal is to find approaches that could be moved toward clinical testing to make these tumors more treatable and delay progression to higher‑grade glioma.

Why it matters

Potential benefit: If successful, this work could lead to new immunotherapy approaches that make IDH‑mutant/ATRX‑loss astrocytomas more responsive to immune attack and slow progression to more aggressive tumors.

How similar studies have gone: Prior studies have shown that IDH‑mutant gliomas have immune‑suppressive features and some preclinical epigenetic or immune‑modulating approaches show promise, but effective immunotherapy for this subtype remains largely unproven in patients.

Where this research is happening

  • Hugo W. Moser Res Inst Kennedy Krieger
    Baltimore, United States
    Active

Researchers

  • Principal investigator: Li, Yunqing — Hugo W. Moser Res Inst Kennedy Krieger
  • Study coordinator: Li, Yunqing

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.