This proposal describes a five-year training program for the development of an academic career in CancerBiology. I have seven years experience as a molecular biologist working in cancer research and I amnowplanning to expand my skills by utilizing mouse models of solid tumors and leukemias. In the first part of theprogram, I will be mentored by Dr. Pier Paolo Pandolfi, a leading cancer biologist who has great experiencein modeling cancer in vivo and who has trained numerous independent investigators. The program will beenriched by the collaboration of Dr. C. Cordon-Cardo, Dr. S. Rafii and Dr. C. Simon. The first part of theaward will be completed at Memorial Sloan-Kettering Cancer Center, a scientific environment ofexcellencethat will provide all the resources necessary to promote the success of this Career Development Award, Research will focus on the study of the regulation of HIF-1 and tumor angiogenesis by the promyelocyticleukemia gene PML, and the fusion protein of acute promyelocytyc leukemia (API), PML-RARa. The transcription factor HIF-1 is the main regulator of cellular responses to hypoxia. HIF-1 is frequentlyupregulated in solid tumors and fosters tumor progression by promoting neoangiogenesis. Conversely, PMLis frequently lost in solid tumors. My preliminary observations indicate that PML is a negative regulator ofHIF-1. Accordingly, Pml-/- cells have higher HIF-1 activity than wild-type cells when subjected to hypoxicstimuli and Pml-/- mice have increased neoangiogenesis in response to ischemia. Finally, I have found thatPML-RARa acts as a constitutive transcriptional co-activator of HIF-1. This observation supports the novelconcept that neoangiogenesis in the bone marrow is an important process in leukemogenesis. In this proposal, I aim at answering the following questions: What is the molecular mechanism by which PML regulates HIF-1? What is the effect of PML loss in the process of neoangiogenesis in solid tumors?And, finally, is HIF activity important in the development of APL? I will address these questions in the following specific aims: 1. Elucidate the molecular mechanisms of HIF-1a regulation by PML; 2. Study the effect of PML loss on tumor angiogenesis and tumor progression invivo; 3. Study the role of HIF-1a overexpression in leukemia in mouse models of APL.The Training Program outlined in this proposal will launch my independent research career.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Scientist Development Award - Research & Training (K01)
Project #
7K01CA118259-02
Application #
7493279
Study Section
Special Emphasis Panel (ZCA1-RTRB-A (M1))
Program Officer
Lohrey, Nancy
Project Start
2006-07-01
Project End
2008-06-30
Budget Start
2007-07-01
Budget End
2008-06-30
Support Year
2
Fiscal Year
2007
Total Cost
$132,030
Indirect Cost
Name
Beth Israel Deaconess Medical Center
Department
Type
DUNS #
071723621
City
Boston
State
MA
Country
United States
Zip Code
02215
Scaglioni, Pier Paolo; Rabellino, Andrea; Yung, Thomas M et al. (2012) Translation-dependent mechanisms lead to PML upregulation and mediate oncogenic K-RAS-induced cellular senescence. EMBO Mol Med 4:594-602