NIH-funded research R01 grant

Boosting virus-based immune therapy for childhood medulloblastoma by targeting RNF2

Official title: Targeting RNF2 to Synergize with Oncolytic Immunovirotherapy to Induce Anti-Cancer Immunity in Medulloblastoma

Funded at University of Tx Md Anderson Can Ctr · NIH-11271139 · Data updated 2026-11-12

This project will try blocking a cancer protein called RNF2 to strengthen a virus-based immune treatment for children with medulloblastoma.

More Medulloblastoma research and trials

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionUniversity of Tx Md Anderson Can Ctr
NIH-funded
Lab location1 site (Houston, United States)
Project startMay 1, 2026
Project endApril 30, 2031
Funding year2026
Award (this year)$421,361
NIH project number1R01NS146081-01
Project IDNIH-11271139 on NIH RePORTER

Who could benefit from this research

Could help

Children with medulloblastoma—especially those with recurrent disease or leptomeningeal spread—who can travel to and receive care at specialized cancer centers may be candidates for this work as it moves into clinical testing.

Less likely to help

Patients whose tumors do not rely on RNF2, who cannot tolerate viral-based therapies, or who are too medically frail for experimental treatment may not benefit from this approach.

What this research studies

From a patient's view, researchers are combining an engineered cancer-killing virus (G207) with methods to block a tumor protein called RNF2 to help the immune system stay active against medulloblastoma. Work will include lab and animal experiments to understand how RNF2 helps tumors escape immune attack and to test whether blocking it makes the virus therapy work better and longer. The team builds on prior safety results with G207 in pediatric brain tumors and will move promising combo approaches toward early clinical testing at specialized centers. The goal is to create a treatment that not only shrinks tumors but also keeps them from coming back by sustaining a strong anti-tumor immune response.

Why it matters

Potential benefit: If successful, this approach could produce safer, longer-lasting treatments that better control tumor spread and reduce the lifelong side effects children often face.

How similar studies have gone: Engineered oncolytic virus G207 has already shown safety and immune activation in pediatric brain tumor trials, but durable responses have been limited, making the RNF2 combination a newer strategy.

Where this research is happening

  • University of Tx Md Anderson Can Ctr
    Houston, United States
    Active

Researchers

  • Principal investigator: Friedman, Gregory K — University of Tx Md Anderson Can Ctr
  • Study coordinator: Friedman, Gregory K

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.