NIH-funded research R01 grant

How healthy and JAK2‑mutant blood stem cells compete in myeloproliferative neoplasms

Official title: Cell Competition in Myeloproliferative Neoplasms

Funded at State University New York Stony Brook · NIH-11131232 · Data updated 2026-11-12

This work looks at whether healthy blood stem cells can keep JAK2‑mutant cells from taking over in people with myeloproliferative neoplasms.

More Neoplasms research and trials

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionState University New York Stony Brook
NIH-funded
Lab location1 site (Stony Brook, United States)
Project startAugust 1, 2022
Project endJune 30, 2027
Funding year2025
Award (this year)$362,298
NIH project number5R01CA266294-04
Project IDNIH-11131232 on NIH RePORTER

Who could benefit from this research

Could help

Ideal candidates for related clinical efforts would be people with myeloproliferative neoplasms (for example, polycythemia vera, essential thrombocythemia, or myelofibrosis) who carry the JAK2V617F mutation or have detectable clonal blood cells.

Less likely to help

People whose disease is driven by non‑JAK2 mutations or who already have transformed acute leukemia may not benefit from strategies focused on JAK2‑driven cell competition.

What this research studies

Researchers grow healthy and JAK2V617F‑mutant blood stem/progenitor cells together in lab dishes and follow which cells expand. They transplant competing cells into animal models to observe how mutant and wild‑type cells behave in a living bone marrow environment. The team measures signals such as the Notch ligand Dlk1 and examines how a mutant marrow environment influences competition. The goal is to find signals or conditions that help healthy cells outcompete mutant clones and prevent progression to frank leukemia.

Why it matters

Potential benefit: If successful, this could point to treatments that boost healthy stem cells or change the marrow environment to reduce mutant clone expansion and lower the risk of leukemia.

How similar studies have gone: Laboratory and animal studies have shown that healthy cells can sometimes suppress mutant clones, but translating these findings into effective patient treatments remains largely unproven.

Where this research is happening

  • State University New York Stony Brook
    Stony Brook, United States
    Active

Researchers

  • Principal investigator: Zhan, Huichun — State University New York Stony Brook
  • Study coordinator: Zhan, Huichun

Related research

Other NIH-funded projects on the same topics.

  • Biomarker clues to catch pancreatic cancer early in cysts

    A study from UC San Diego is testing blood and cyst-fluid markers to help tell high-risk pancreatic cysts from low-risk ones so that people with pancreatic cysts can get the right care sooner.

    NIH research University of California, San Diego · La Jolla, United States · NIH-11420592

  • Myeloproliferative Neoplasm Research Consortium

    A large research collaboration across multiple centers aims to improve survival for patients with myelofibrosis and related myeloproliferative neoplasms through coordinated laboratory, translational, and clinical work.

    NIH research Icahn School of Medicine at Mount Sinai · New York, United States · NIH-11399011

  • Understanding how different CALR mutations drive certain blood cancers

    This grant explores how two CALR mutation types cause myeloproliferative neoplasms and could lead to better treatments for people with these blood cancers.

    NIH research Utah State Higher Education System--University of Utah · Salt Lake City, United States · NIH-11393750

  • Cell Competition in Myeloproliferative Neoplasms

    This NIH grant explores how healthy and mutant blood stem cells interact in certain blood cancers to understand why some patients progress and how future therapies might help.

    NIH research State University New York Stony Brook · Stony Brook, United States · NIH-11380052

  • Targeting ERK’s brake pedals to slow cancer progression

    Aims to block the parts of ERK signaling that speed up cancer progression, by guiding drugs to the substrate-binding domains that act like accelerator pedals in myeloproliferative neoplasms and related cancers.

    NIH research Research Inst of Fox Chase Can Ctr · Philadelphia, United States · NIH-11364927

  • Biomarker work to predict pancreatic IPMN cancer risk

    A Duke University researcher is testing biomarkers to tell which pancreatic IPMN cysts are likely to become invasive cancer.

    NIH research Duke University · Durham, United States · NIH-11361607

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.