Genetic and molecular signs that predict aggressive prostate cancer

Project 1: Molecular Predictors of Prostate Cancer Progression and Mortality

NIH-funded research Fred Hutchinson Cancer Center · NIH-11181522

This project will find out whether inherited DNA changes and a combined genetic risk score can help identify men—especially men of African ancestry—who face higher risk of aggressive or deadly prostate cancer.

Quick facts

Grant typeNIH-funded research
Study typeNIH-funded research
Funding institutionFred Hutchinson Cancer Center NIH-funded
Lab location1 site (Seattle, United States)
Project IDNIH-11181522 on NIH RePORTER

What this research studies

This project will recruit men with prostate cancer from diverse ancestries, with an emphasis on non-European and African ancestry patients, to study their inherited genes and tumor tissue. Researchers will test blood and tumor samples to look for rare inherited changes in DNA repair genes like BRCA2 and combine that information with a multi-ancestry polygenic risk score (PRSm). They will build a clinical-grade paired tumor-germline assay, identify which specific genetic variants have the biggest effects, and link these genetic markers to cancer clinical features and outcomes. Finally, the team will offer a tailored prostate cancer screening clinical trial for people judged to be at highest risk based on these combined genetic markers.

Who could benefit from this research

Good fit: Men with prostate cancer—particularly those of African ancestry, those with a family history, or those known to carry DNA repair gene variants—are the best fit for participation.

Not a fit: People without prostate cancer, women, or men whose cancers are driven by non-genetic factors may not receive direct benefit from this project.

Why it matters

Potential benefit: If successful, this work could help doctors spot men at highest risk earlier and personalize screening and treatment to prevent advanced prostate cancer.

How similar studies have performed: Previous research has shown links between rare DNA repair gene variants and polygenic risk scores with prostate cancer risk, but combining them into a clinical-grade test and applying this approach in diverse populations and screening trials is relatively new.

Where this research is happening

Seattle, United States

Researchers

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 below.
Conditions Breast Cancer 2 Gene
Last reviewed 2026-06-13 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.