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Young Investigator Grants

Young Investigator grants are designed to fill the critical need for startup funds for less experienced researchers to pursue promising research ideas. Eligible applicants may apply during their fellowship training or early in their research careers but must not have achieved an appointment higher than Instructor. These grants encourage and cultivate the best and brightest researchers of the future and lead to long-term research projects. The Young Investigator grant offers up to $60,000 per year for three years.

Massachusetts General Hospital

Infant acute leukemias (arising in children less than one year old) makes up a unique subset of leukemias that are particularly lethal and that are characterized by recurrent mutations in one gene. This gene has been termed the mixed lineage leukemia (or MLL) gene, and mutations in MLL are found in the majority of infant leukemias as well as in smaller proportions of childhood and adult leukemias. The mutations in MLL are intriguing, because they are the result of chromosomal breakage which abnormally joins the MLL gene to a variety of partner genes.

Principal Investigator Name: 

David Sykes

Project Title: 

Targeting the Mechanism of Differentiation Arrest in a Novel Model of Acute Leukemia

Year Awarded: 

2011

Cancer Research Category: 

Category of Grant: 

Medical, Nurse Researcher, Quality of LIfe: 

Institution: 

Files: 

Vanderbilt University Medical Center

T cell acute lymphoblastic leukemia (T-ALL) is an aggressive cancer of white blood cells which affects both children and adults. Many children with T-ALL can be cured with very intensive chemotherapy, but there are significant long term health problems associated with this therapy. A major goal for T-ALL is to develop new therapies that can help reduce the burden of treatment and offer cures to the approximately 20% of pediatric patients who succumb to the disease.

Principal Investigator Name: 

Emmanuel Volanakis

Project Title: 

Targeting polycomb-mediated epigenetic silencing in T cell acute lymphoblastic leukemia

Year Awarded: 

2011

Cancer Research Category: 

Category of Grant: 

Medical, Nurse Researcher, Quality of LIfe: 

Institution: 

Baylor College of Medicine

Delay in blood cell count recovery after chemotherapy is the most commonly observed toxicity in pediatric acute myeloid leukemia (AML), and 80% of patients develop severe toxicities during treatment.  Delay in therapy due to a low white blood cell (WBC) count places individuals at risk for severe infections, and is associated with an increased mortality.  We are investigating genetic markers for risk for AML treatment-related toxicities, such as unexpectedly prolonged periods of low WBC count after chemotherapy.  The genetic marker we are studying is an enzyme called telomerase, which maint

Principal Investigator Name: 

Maria Gramatges

Project Title: 

Telomeres and Telomerase in Pediatric Acute Myeloid Leukemia

Year Awarded: 

2011

Cancer Research Category: 

Category of Grant: 

Medical, Nurse Researcher, Quality of LIfe: 

Institution: 

University of California San Francisco

Second malignant neoplasms (SMNs) are late complications arising after exposure to chemotherapy and radiotherapy, accounting for most of the ~90,000 new cancers that are diagnosed annually in the United States in persons who previously had a histologically distinct malignancy.

Principal Investigator Name: 

Jean Nakamura

Project Title: 

Investigation of Genetic and Molecular Mechanisms of Second Malignant Neoplasms in a Mouse Model

Year Awarded: 

2011

Cancer Research Category: 

Category of Grant: 

Medical, Nurse Researcher, Quality of LIfe: 

Institution: 

Fred Hutchinson Cancer Research Center

Pediatric acute lymphoblastic leukemia (ALL) is the most common childhood cancer, with approximately 2400 new cases/year in the United States.  Patients are put into remission using chemotherapy, and over 70% stay in remission.  If a patient relapses, it is hard to achieve a long-term cure, and they often succumb to their disease.  The best chance for maintaining a remission after relapse is often through a stem cell transplant (SCT), in which the patient's bone marrow is replaced with hematopoietic stem cells (HSC) from either a donor or cord blood unit.  Part of the reason a cure is achie

Principal Investigator Name: 

Rebecca Gardner

Project Title: 

Engineering A Graft Versus Leukemia Effect into Cord Blood Transplant for Acute Lymphoblastic Leukemia

Year Awarded: 

2011

Cancer Research Category: 

Category of Grant: 

Medical, Nurse Researcher, Quality of LIfe: 

Institution: 

Massachusetts General Hospital

It has been shown that metabolism, which comprises a range of biochemical processes essential for cell functioning, can play a role in the causation of cancer including leukemias. Certain leukemia cells have been shown to have cancer initiating or 'stem cell' potential.  There is little knowledge about the role that metabolism plays in the maintenance of leukemia stem cells.
 

Principal Investigator Name: 

Rushdia Yusuf

Project Title: 

The Role of Metabolism in MLL-AF9 Leukemia Initiation

Year Awarded: 

2010

Cancer Research Category: 

Category of Grant: 

Institution: 

St. Jude Children's Research Hospital

Cure rates of childhood acute lymphoblastic leukemia (ALL) have improved dramatically in the past decades. However, in 15-20% of children with ALL, the leukemia comes back after therapy and most children who relapse eventually succumb to the disease. Relapsed ALL is in fact one of the leading cause of death in children with cancer. Most importantly, ALL relapse is significantly more frequent in Hispanic children compared to Caucasians, and the underlying causes are largely unknown.

Principal Investigator Name: 

Jun Yang

Project Title: 

The role of PDE4B in Racial Disparities in Outcome of Childhood Acute Lymphoblastic Leukemia

Year Awarded: 

2010

Cancer Research Category: 

Category of Grant: 

Medical, Nurse Researcher, Quality of LIfe: 

Institution: 

Stanford University

Traditional approach targeting only genetic factors and non-cancer stem cells for drug discovery appears insufficient to combat cancer diseases especially in the category of childhood leukemia caused by MLL gene mutation which occurs frequently in infants and children and associates with poor survival rate. It is becoming clear that cancer cells transformation is initiated and maintained by both genetic and epigenetic mechanisms.

Principal Investigator Name: 

Hon-Kit Wong

Project Title: 

Identification and Characterization of an Epigenetic Program that Maintains the Self-Renewal of MLL Myeloid Leukemia Stem Cells

Year Awarded: 

2010

Cancer Research Category: 

Category of Grant: 

Institution: 

Cincinnati Children's Hospital Medical Center

After brain cancer, the most common solid tumor in children is neuroblastoma. Some versions of neuroblastoma are highly deadly, with fewer than half of patients cured despite surgery, radiation, high dose chemotherapy, bone marrow transplantation, and treatment with vitamin A forms that cause cells to mature and stop dividing. It is widely believed by most pediatric hematologists/oncologists that we have reached a plateau in our use of these treatments, and further refinements will only bring minimal improvements in increasing patient survival.

Principal Investigator Name: 

Pin-Yi Wang

Project Title: 

Virotherapy on Primary Neuroblastoma Cells

Year Awarded: 

2010

Cancer Research Category: 

Category of Grant: 

Institution: 

The Children's Hospital of Philadelphia

Low-grade glioma is one of the most common types of brain tumor that occur in children. Until recently, little was known about the molecular events that led to glioma formation. As a direct result of this paucity of information, low-grade glioma directed treatment has significantly lagged behind advances made in other childhood malignancies. Children with unresectable or recurrent/disseminated low-grade gliomas have been left with few treatment options. Their event free and overall survival rates have been dismal.

Principal Investigator Name: 

Angela Waanders, MD, MPH

Project Title: 

Characterization and Targeting of Novel Activating BRAF Mutations in Pediatric Brain Tumors

Year Awarded: 

2010

Cancer Research Category: 

Category of Grant: 

Institution: 

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