NIH-funded research R01 grant

Understanding the differences between two types of mutations in a protein linked to blood cancers.

Official title: The Pathophysiology of Type 1 Versus Type 2 Mutant Calreticulin-Drivenmyeloproliferative Neoplasms

Funded at University of Utah · NIH-11158469 · Data updated 2026-11-12

This study is looking at how different mutations in a protein called calreticulin affect the progression of myeloproliferative neoplasms (MPNs) and aims to find new treatments, inviting patients with MPNs to help by participating in genetic testing and check-ups.

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionUniversity of Utah
NIH-funded
Lab location1 site (Salt Lake City, United States)
Project startAugust 1, 2024
Project endAugust 31, 2027
Funding year2024
Award (this year)$422,510
NIH project number7R01HL165119-03
Project IDNIH-11158469 on NIH RePORTER

Who could benefit from this research

Could help

Ideal candidates for participation are individuals diagnosed with myeloproliferative neoplasms, particularly those with calreticulin mutations.

Less likely to help

Patients without myeloproliferative neoplasms or those with different underlying genetic causes may not benefit from this research.

What this research studies

This research investigates the pathophysiology of myeloproliferative neoplasms (MPNs), specifically focusing on the differences between type 1 and type 2 mutations in the calreticulin protein. By examining how these mutations affect disease progression and patient outcomes, the study aims to identify potential new therapies that could more effectively treat these conditions. The approach includes analyzing the genetic and molecular mechanisms behind these mutations and their impact on signaling pathways involved in blood cell production. Patients with MPNs may have the opportunity to contribute to this research through genetic testing and clinical assessments.

Why it matters

Potential benefit: If successful, this research could lead to the development of targeted therapies that improve treatment outcomes for patients with myeloproliferative neoplasms.

How similar studies have gone: Previous research has shown promising results in understanding the role of genetic mutations in blood cancers, suggesting that this approach could yield valuable insights.

Where this research is happening

  • University of Utah
    Salt Lake City, United States
    Active

Researchers

  • Principal investigator: Elf, Shannon Elisabeth — University of Utah
  • Study coordinator: Elf, Shannon Elisabeth

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.