NIH-funded research Fellowship grant

Understanding how NCK1 influences blood cell production in certain blood disorders

Official title: The role of NCK1 in CSF3R-driven myeloproliferative neoplasms

Funded at Oregon Health & Science University · NIH-11000787 · Data updated 2026-11-12

This study is looking at how a protein called NCK1 works with a receptor that helps make white blood cells, and it aims to find new ways to treat people with blood disorders that cause too many of these cells to be produced.

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Quick facts

Grant typeFellowship grant
Study typeNIH-funded research
Funding institutionOregon Health & Science University
NIH-funded
Lab location1 site (Portland, United States)
Project startDecember 1, 2022
Project endNovember 30, 2025
Funding year2025
Award (this year)$48,974
NIH project number5F31HL165919-03
Project IDNIH-11000787 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 mutations in the CSF3R gene.

Less likely to help

Patients with blood disorders not related to CSF3R mutations or those with other types of blood cancers may not benefit from this research.

What this research studies

This research investigates the role of a protein called NCK1 in the signaling pathways activated by the Colony Stimulating Factor 3 Receptor (CSF3R), which is crucial for the production of neutrophils, a type of white blood cell. The study focuses on myeloproliferative neoplasms (MPNs), where mutations in CSF3R lead to excessive neutrophil production. By identifying how NCK1 interacts with CSF3R and influences the MAPK signaling pathway, the research aims to uncover new therapeutic targets that could improve treatment options for patients with these blood disorders.

Why it matters

Potential benefit: If successful, this research could lead to new treatments that better control blood cell production in patients with myeloproliferative neoplasms.

How similar studies have gone: Other research has shown promising results in targeting similar signaling pathways in blood disorders, suggesting that this approach may also yield beneficial outcomes.

Where this research is happening

  • Oregon Health & Science University
    Portland, United States
    Active

Researchers

  • Principal investigator: Maniaci, Breanna Nicole — Oregon Health & Science University
  • Study coordinator: Maniaci, Breanna Nicole

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.