NIH-funded research P01 program project

Understanding how inflammation and biology drive blood cancer evolution

Official title: Intrinsic and Extrinsic FactorsDriving Clonal Evolution and Disease Progression in Myeloproliferative Neoplasms

Funded at Washington University · NIH-11348769 · Data updated 2026-11-12

A large, multi-project program at Washington University is exploring how inflammatory signals and cell-intrinsic factors work together to drive progression of myeloproliferative neoplasms in people.

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Quick facts

Grant typeP01 program project
Study typeNIH-funded research
Funding institutionWashington University
NIH-funded
Lab location1 site (Saint Louis, United States)
Project startAugust 15, 2026
Project endJuly 31, 2031
Funding year2026
Award (this year)$2,355,825
NIH project number1P01HL185367-01
Project IDNIH-11348769 on NIH RePORTER

Who could benefit from this research

Could help

Patients with myeloproliferative neoplasms, including those with JAK2 mutations, who can contribute biospecimens or participate in related clinical studies.

Less likely to help

Patients without MPN-related biology or those not eligible for any associated clinical or biospecimen studies may not benefit.

What this research studies

This Program Project Grant brings together four research projects and three cores to study why certain blood cancers called myeloproliferative neoplasms progress and spread. Researchers will look at how inflammatory cytokines interact with cellular pathways to promote clonal expansion and disease progression, using advanced molecular and bioinformatics methods. The effort emphasizes collaboration among experienced scientists and leverages shared biospecimens and pathology resources to understand disease mechanisms. The work aims to generate integrated insights that could inform new approaches to diagnosis and treatment for patients with MPNs.

Why it matters

Potential benefit: If successful, the program could identify new targets and strategies to slow or halt MPN progression and improve patient outcomes.

How similar studies have gone: The project builds on an established track record of collaboration and prior publications among the investigators, indicating a solid foundation for success.

Where this research is happening

  • Washington University
    Saint Louis, United States
    Active

Researchers

  • Principal investigator: Oh, Stephen — Washington University
  • Study coordinator: Oh, Stephen

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.