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Innovation Grants

These grants are designed to provide critical and significant seed funding for experienced investigators with a novel and promising approach to finding causes and cures for childhood cancers. A Letter of Intent is required. The Innovation Award amount totals $250,000 over two years. The Award may not be renewed, however, one no cost extensions are allowable.

In Situ CD19.CAR-T Generation Using TRIDENT System for Pediatric B Cell Malignancies

Cancer is the leading cause of death by disease for children in the United States, and B cell malignancy is the most common form of childhood cancer, accounting for more than 30% of all childhood cancers. Although outcomes in pediatric patients with B cell lymphoma have improved in recent decades, with survival rates of >80%, relapse or progression are nearly universally fatal for children and young adults with relapsed and refractory mature B cell lymphoma.

Principal Investigator Name: 

Masataka Suzuki, PhD

Project Title: 

In Situ CD19.CAR-T Generation Using TRIDENT System for Pediatric B Cell Malignancies

Year Awarded: 

2023

Cancer Research Category: 

Category of Grant: 

Medical, Nurse Researcher, Quality of LIfe: 

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Inhibition of translation initiation as a novel therapeutic strategy against MYCN-amplified neuroblastoma

The goal of this project is to test a novel strategy for disrupting the effects of MYCN amplification, which is seen in over 50% of high risk neuroblastoma patients. Although the association of MYCN amplification with a poor outcome is well established, attempts to directly target MYCN have been challenging. Therefore, we propose to tackle one of the consequences of amplified MYCN that enables abnormal cell growth, that of increased protein expression (translation). Proteins are the “doers” in the cell and originate from RNA.

Principal Investigator Name: 

Rani George, MD, PhD

Project Title: 

Inhibition of translation initiation as a novel therapeutic strategy against MYCN-amplified neuroblastoma

Year Awarded: 

2022

Cancer Research Category: 

Category of Grant: 

Medical, Nurse Researcher, Quality of LIfe: 

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Developing Novel Transcription Factor PROTACs to Disrupt the HMGA1 Epigenome in Relapsed Leukemia

Acute lymphoblastic leukemia (ALL) is the most common form of childhood leukemia and the leading cause of death in children with cancer. While therapy is often curative, ~10% of children will relapse with recurrent disease and abysmal outcomes. Unfortunately, recent efforts to increase the dose or frequency of standard therapy have failed to prevent relapse. Thus, we have reached the ceiling of efficacy for current therapy and new strategies are needed. Here, we take a novel approach by focusing on HMGA1 proteins as drivers of relapse in leukemia.

Principal Investigator Name: 

Linda Resar, MD and Jian Jin, PhD

Project Title: 

Developing Novel Transcription Factor PROTACs to Disrupt the HMGA1 Epigenome in Relapsed Leukemia

Year Awarded: 

2022

Cancer Research Category: 

Category of Grant: 

Medical, Nurse Researcher, Quality of LIfe: 

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Epigenetic Enhancement of MHCI to Augment Neuroblastoma Immunotherapy

Half of all neuroblastoma patients are diagnosed with high-risk neuroblastoma. Even with the recent addition of immunotherapy, which has been proven to help, only ~ 50% of children with high-risk disease are cured. Laboratory studies have identified three characteristics that make high-risk-neuroblastoma harder to cure using the current clinical regimen of chemotherapy, surgery, radiation and immunotherapy.

Principal Investigator Name: 

Paul Sondel, MD, PhD and Amy Erbe-Gurel, PhD

Project Title: 

Epigenetic Enhancement of MHCI to Augment Neuroblastoma Immunotherapy

Year Awarded: 

2022

Cancer Research Category: 

Category of Grant: 

Medical, Nurse Researcher, Quality of LIfe: 

Institution: 

Molecular circuitry of fibrolamellar carcinoma

Fibrolamellar carcinoma is an liver cancer of adolescents and young adults. Currently the only effective treatment is surgery, but this is only possible in a subset of cases. Chemotherapy and targeted therapies have not been successful to date. Important features of this cancer include the presence of an abnormal gene in virtually every patient. This abnormal gene, referred to as DNAJB1-PRKACA, is found in virtually all patients.

Principal Investigator Name: 

Nabeel Bardeesy, PhD

Project Title: 

Molecular circuitry of fibrolamellar carcinoma

Year Awarded: 

2022

Cancer Research Category: 

Category of Grant: 

Medical, Nurse Researcher, Quality of LIfe: 

Institution: 

Developmental origins of leukemia in Down Syndrome

A third of babies with Down Syndrome are born with an abnormal blood production called TAM (transient abnormal myelopoiesis), which is an expansion of immature, leukemia-like, blood cells that carry a mutation called Gata1s. TAM is associated with a significant increase in death shortly after birth, and roughly 1 in 4 babies that survive the neonatal period develops leukemia before the age of 4. It is not well understood how or when TAM arises during fetal life.

Principal Investigator Name: 

James Palis, MD & Laurie Steiner, MD

Project Title: 

Developmental origins of leukemia in Down Syndrome

Year Awarded: 

2022

Cancer Research Category: 

Category of Grant: 

Medical, Nurse Researcher, Quality of LIfe: 

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Blocking the Evil Messenger in MYCN-driven High-risk Neuroblastoma

MYCN is a potent cancer-causing gene, and its elevated activity drives the initiation, progression, and treatment resistance of a broad spectrum of childhood cancers. Neuroblastoma is the most common extracranial solid tumor among children, with approximately half of them characterized as high-risk, which spread to distant organs rapidly and result in less than 50% survival rates.

Principal Investigator Name: 

Hui Feng, Md, PhD

Project Title: 

Blocking the Evil Messenger in MYCN-driven High-risk Neuroblastoma

Year Awarded: 

2022

Category of Grant: 

Medical, Nurse Researcher, Quality of LIfe: 

Institution: 

Targeted nanoparticle-mediated “cold”-to-“hot” reprogramming of the tumor microenvironment of high-risk neuroblastoma

This project seeks to develop a targeted nanoparticle therapy that harnesses proinflammatory innate immune cells to reprogram TME immunity in high-risk NB. Currently, survival for high-risk metastatic NB remains ~50% at 5 years, even with chemotherapy given at maximal tolerated dosing, which itself imparts debilitating long-term sequelae in >90% of survivors.

Principal Investigator Name: 

Prabhani Atukorale, PhD & Jason Shohet, MD, PhD

Project Title: 

Targeted nanoparticle-mediated “cold”-to-“hot” reprogramming of the tumor microenvironment of high-risk neuroblastoma

Year Awarded: 

2022

Cancer Research Category: 

Category of Grant: 

Medical, Nurse Researcher, Quality of LIfe: 

Institution: 

Impact of STAG2 loss on DNA Damage and Immunobiology in Ewing sarcoma

Ewing sarcoma is a cancer most often diagnosed in teenagers. We know that some changes in the make-up of Ewing tumors make them more likely to be aggressive and spread to other parts of the body. When Ewing sarcoma spreads to other parts of the body, like the lung, it is very hard to cure. Radiation is one therapy used to treat Ewing sarcoma in the lungs. Radiation can directly damage tumor cells and can also "call" immune cells into the tumor to help attack cancer cells.

Principal Investigator Name: 

Kelly Bailey, MD, PhD

Project Title: 

Impact of STAG2 loss on DNA Damage and Immunobiology in Ewing sarcoma

Year Awarded: 

2022

Cancer Research Category: 

Category of Grant: 

Medical, Nurse Researcher, Quality of LIfe: 

Institution: 

Isoform-specific TNC-redirected T cell Therapy for DIPG

DIPG remains an incurable brain tumor since current therapies, including radiation and chemotherapy, cannot destroy all DIPGs cells. Immunotherapy holds the promise to improve outcomes for children with DIPG since immune cells kill tumor cells through different mechanisms than radiation and chemotherapy. Among different forms of immunotherapy, an immunotherapy consisting of immune cells known as T cells as garnered significant excitement.

Principal Investigator Name: 

Stephen Gottschalk, MD and Giedre Krenciute, PhD

Project Title: 

Isoform-specific TNC-redirected T cell Therapy for DIPG

Year Awarded: 

2022

Cancer Research Category: 

Category of Grant: 

Medical, Nurse Researcher, Quality of LIfe: 

Institution: 

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