NIH-funded research Career grant

Understanding how genetic changes affect blood disorders and fibrosis progression

Official title: Investigating High-Risk Epigenetic Modifying Alterations on JAK2VF Dependency and Fibrotic Progression in Myeloproliferative Neoplasms (MPNs)

Funded at University of Tx Md Anderson Can Ctr · NIH-11096109 · Data updated 2026-11-12

This study is looking at how certain genetic changes, especially the JAK2VF mutation, affect the progression of myeloproliferative neoplasms (MPNs) and how well treatments work, with the hope of finding better ways to help patients like you.

Quick facts

Grant typeCareer grant
Study typeNIH-funded research
Funding institutionUniversity of Tx Md Anderson Can Ctr
NIH-funded
Lab location1 site (Houston, United States)
Project startJune 1, 2024
Project endSeptember 30, 2028
Funding year2024
Award (this year)$167,616
NIH project number7K08HL169905-02
Project IDNIH-11096109 on NIH RePORTER

Who could benefit from this research

Could help

Ideal candidates for this research are patients diagnosed with myeloproliferative neoplasms, particularly those with the JAK2VF mutation and associated genetic alterations.

Less likely to help

Patients without myeloproliferative neoplasms or those whose conditions are unrelated to the JAK2VF mutation may not benefit from this research.

What this research studies

This research investigates the role of specific genetic mutations in myeloproliferative neoplasms (MPNs), which are blood disorders characterized by the overproduction of blood cells and fibrosis in the bone marrow. The study focuses on the JAK2VF mutation and its interaction with other genetic alterations that may worsen the disease and hinder treatment effectiveness. By using advanced mouse models, researchers aim to uncover how these genetic changes influence disease progression and response to therapies, potentially leading to new treatment strategies for patients.

Why it matters

Potential benefit: If successful, this research could lead to improved treatment options for patients with myeloproliferative neoplasms by targeting the underlying genetic mechanisms of the disease.

How similar studies have gone: Previous research has shown promising results in targeting genetic mutations in blood disorders, indicating that this approach may lead to significant advancements in treatment.

Where this research is happening

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

Researchers

  • Principal investigator: Dunbar, Andrew Jeffrey — University of Tx Md Anderson Can Ctr
  • Study coordinator: Dunbar, Andrew Jeffrey

Related research

Other NIH-funded projects on the same topics.

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  • 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.