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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.

Dana-Farber Cancer Institute

Background
New treatments are urgently needed to combat relapsed and refractory pediatric cancers. A specialized group of proteins, called the BCL-2 family, regulates the natural balance between cellular life and death, ensuring that essential cells are preserved and damaged cells eliminated.

Principal Investigator Name: 

Loren Walensky, MD, PhD

Project Title: 

Reactivating Apoptosis in Refractory Pediatric Cancer by Molecular Inhibition of MCL-1

Year Awarded: 

2013

Cancer Research Category: 

Category of Grant: 

Medical, Nurse Researcher, Quality of LIfe: 

Institution: 

Therapeutically Targeting a Tumor Suppressor Complex in Aggressive Pediatric Cancers

Background

Principal Investigator Name: 

Charles Roberts, MD, PhD

Project Title: 

Therapeutically Targeting a Tumor Suppressor Complex in Aggressive Pediatric Cancers

Year Awarded: 

2013

Cancer Research Category: 

Category of Grant: 

Medical, Nurse Researcher, Quality of LIfe: 

Institution: 

The Children's Hospital of Philadelphia

Background
Cancers arise because of mutations (or mistakes) in their genes. For many cancers, the identification of their most important cancer genes, and an improved understanding of how these effect the cancer cells, has led to new treatments. Neuroblastoma is a childhood tumor that is often difficult to cure.

Principal Investigator Name: 

Michael Hogarty, MD

Project Title: 

Epigenetic Characterization of the Neuroblastoma Driver Genes ARID1A and ARID1B

Year Awarded: 

2013

Cancer Research Category: 

Category of Grant: 

Medical, Nurse Researcher, Quality of LIfe: 

Institution: 

Lucile Packard Children's Hospital at Stanford University School of Medicine

Background
Inappropriate activation of the Hedgehog signaling pathway can promote the onset and/or progression of several pediatric cancers, including medulloblastoma, rhabdomyosarcoma, diffuse intrinsic pontine glioma, and Ewing's sarcoma. Hedgehog pathway inhibitors therefore provide new hope to children afflicted with these diseases, and drugs that target the transmembrane signaling protein Smoothened have induced dramatic tumor regressions in the clinic.

Principal Investigator Name: 

James Chen, PhD

Project Title: 

Next-Generation Therapies for Hedgehog Pathway-Dependent Tumors

Year Awarded: 

2013

Cancer Research Category: 

Category of Grant: 

Medical, Nurse Researcher, Quality of LIfe: 

Institution: 

Massachusetts General Hospital

Background
The aggressive and unpredictable behavior of relapsed T-cell acute lymphoblastic leukemia (T-ALL) presents a major clinical challenge, as relapsed disease continues to have a dismal prognosis in both children and adults. A major hurdle in the development of new chemotherapies is identifying drugs that specifically kill malignant T cells, while leaving normal cells untouched.

Principal Investigator Name: 

David Langenau, PhD

Project Title: 

Novel Therapeutic Targets in Relapse T-cell Acute Lymphoblastic Leukemia

Year Awarded: 

2013

Cancer Research Category: 

Category of Grant: 

Medical, Nurse Researcher, Quality of LIfe: 

Institution: 

Cincinnati Children's Hospital Medical Center

Background
The overall outcome of acute myeloid leukemia (AML) remains unacceptable. AML1-ETO (AE), the product of chromosome translocation 8;21, is the most frequently observed fusion gene in childhood acute myeloid leukemia. As a transcription factor, AML1-ETO interferes with normal blood production by disturbing gene expression normally regulated by the AML1 protein. There are currently no targeted therapies available for AML1-ETO-expressing AML.

Principal Investigator Name: 

Yi Zheng, PhD

Project Title: 

Therapeutic Targeting of LARG-RhoA Signaling Axis in Childhood Leukemia

Year Awarded: 

2013

Cancer Research Category: 

Category of Grant: 

Medical, Nurse Researcher, Quality of LIfe: 

Institution: 

Research Institute of the McGill University Health Centre

Background
miRNAs are small molecules involved in almost every aspect of normal cellular function throughout the human body. The DICER1 protein is one of the proteins responsible for fabricating the right size, type and quantity of miRNAs in our cells. We know from recent studies that inherited mutations in the DICER1 gene predispose someone to cancer. These mutations are rare but cause tumors that occur early in life, affecting children and young adults (one example is malignant lung cysts in infants, named pleuropulmonary blastoma, which can be lethal).

Principal Investigator Name: 

William Foulkes, MD, PhD

Project Title: 

DICER1, MicroRNAs and Pediatric Cancer: An Emerging Story

Year Awarded: 

2013

Cancer Research Category: 

Category of Grant: 

Medical, Nurse Researcher, Quality of LIfe: 

Institution: 

Files: 

Northwestern University Medical School

Background
Neuroblastoma is the third most common cancer in children and the most common malignancy in infants. Although treatment options are improving, survival rates for newly diagnosed patients remain at around 70%. Metastatic disease at the time of diagnosis confers a poorer prognosis, and the 3-year survival rate for patients with recurrent disease is only around 30%.

Principal Investigator Name: 

Richard Longnecker, PhD

Project Title: 

An Oncolytic Herpes Simplex Virus Restricted in Entry to Neuroblastoma Cells

Year Awarded: 

2013

Cancer Research Category: 

Category of Grant: 

Medical, Nurse Researcher, Quality of LIfe: 

Institution: 

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