Awarded Grants

Awarded Grants

Jumpstart, 2025, Grant Assistance Program, Bloom Syndrome Million Dollar Bike Ride Jumpstart, 2025, Grant Assistance Program, Bloom Syndrome Million Dollar Bike Ride

An Evaluation of Gene Modification Strategies for Bloom Syndrome

Caroline Kuo

University of California, Los Angeles

$50,000

Awardee: Caroline Kuo

Institution: University of California, Los Angeles

Awarded: $50,000

Funding Period: April 1, 2025 – March 31, 2026

Summary: To date, no studies have assessed the feasibility of gene modification as a potential treatment for Bloom syndrome. This project outlines specific aims that include proof-of-concept experiments essential for evaluating the viability of gene therapy as a therapeutic option for this condition

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Jumpstart, 2025, Grant Assistance Program, Bloom Syndrome Million Dollar Bike Ride Jumpstart, 2025, Grant Assistance Program, Bloom Syndrome Million Dollar Bike Ride

The Somatic Mutational Landscape Of Blm-Deficient Tumors: Finding Clues for Future Therapeutic Opportunities

Richarda de Voer

Radboud University Medical Center (Stichting Radboud Fonds)

$150,000

Awardee: Richarda de Voer

Institution: Radboud University Medical Center (Stichting Radboud Fonds)

Awarded: $150,000

Funding Period: April 1, 2025 – March 31, 2027

Summary: Despite cancer surveillance strategies >80% of individuals with Bloom syndrome (BSyn) will have developed a malignancy by the age of 40 years. Treatment of malignancies in individuals with BS is still mostly based on standard-of-care treatments. With this proposal we aim to unravel the (mutational) mechanisms responsible for tumor initiation and progression in individuals with BSyn. We expect to gain insights into the processes relevant for tumor development in individuals with BSyn, leading to clues for future therapeutic opportunities. We will repurpose archived tumors from individuals with BSyn to:

1. Perform whole-exome or whole-genome sequencing to determine the somatic single base and small indel mutation landscape, investigate mutational signatures of defective DNA repair, mutated driver genes and identify potential signs of homologous recombination deficiency (HRD);

2. Explore the immune landscape of tumors using multiplex immunohistochemistry.

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