Biosketch

Dr. Alitalo discovered vascular growth factors that regulate growth of lymphatic vessels (lymphangiogenesis), and characterized the involved receptors and signalling mechanisms. He isolated and characterized the arterial endothelial tyrosine kinase Bmx and endothelial receptor tyrosine kinase Tie1, which together with Tie2 forms the receptor complex for angiopoietins involved regulation of vascular permeability, inflammation, angiogenesis and lymphangiogenesis. He also isolated and cloned the vascular endothelial growth factor (VEGF) receptor-3, purified and cloned its ligand, the first lymphangiogenic growth factor, VEGF-C. He was central in the characterization of VEGF-D, another VEGFR3 ligand, and VEGF-B, a growth factor for coronary and adipose vasculature. Studies in his laboratory have demonstrated VEGF-C induced tumor angiogenesis and lymphangiogenesis, intralymphatic tumor growth, VEGF-C association with tumor metastasis and its inhibition by blocking the VEGFR-3 signal transduction pathway. Inhibitors of this pathway from his laboratory are phase 2 clinical trial in age-related macular degeneration and diabetic macular edema. He demonstrated mechanisms of lymphedema, and developed growth factor therapy for lymphedema, which has now undergone a phase 2 clinical trial. His recent findings include the discovery of meningeal lymphatic vessels, a molecular model of angiopoietin-Tie receptor complex at endothelial cell-cell junctions, and characterization of angiopoietin-2 mutations in human lymphedema.

Research Interests

Dr. Alitalo is best known for his work on oncogenes and mechanisms of angiogenesis. He discovered lymphangiogenesis its regulation by growth factors, receptors and signaling mechanisms. He has isolated and characterized several tyrosine kinases including the endothelial receptor tyrosine kinase Tie1, which is related to the Tie2 receptor for angiopoietins and implicated in tumor angiogenesis. He cloned the vascular endothelial growth factor (VEGF) receptor-3, purified and cloned its ligand VEGF-C, and showed that the VEGF-C/VEGFR-3 pathway is required for angiogenesis and lymphangiogenesis. He was also central in the cloning and characterization of the VEGF-B. His laboratory is curerntly studying its function as a coronary vascular growth factor and metabolic regulator in the heart. Studies in his laboratory have demonstrated VEGF-C induced tumor angiogenesis and lymphangiogenesis, intralymphatic tumor growth, and VEGF-C association with tumor metastasis and its inhibition by blocking the VEGFR-3 signal transduction pathway. The inhibitors of these pathways from his laboratory have now entered phase I clinical trials. He is also interested in molecular therapies for lymphedema, which are entering clinical trials. Recent work in his laboratory heve also led to studies of the homeobox transcription factor Prox1 in colon carcinoma stem cells and tumor progression.

Membership Type

International Member

Election Year

2013

Primary Section

Section 41: Medical Genetics, Hematology, and Oncology

Secondary Section

Section 22: Cellular and Developmental Biology