Name : DUBREUIL Patrice, Charles
1981 : PhD thesis of Immunology : Immunology Centre of Marseille-Luminy (CIML). Director of thesis (F.Lemonnier) – Research fellowship (DGRST)
1985 : Permanent position INSERM. 2005 : DR1
Group leader at the Cancerology Research Centre of Marseille (CRCM) U1068 Marseille
Team : "Signalling, Hematopoiesis and Mechanism of Oncogenesis" AERES label A
Post doctoral training and awards
1981-1984 : Post Doctoral Position in Immunology Centre de Marseille Luminy
1984: Cellular Biology Lab (P.Mannoni). University of Edmonton, Canada. Research fellowship of UICC
1985-1988: Post Doctoral Position - Molecular Biology lab; INSERM 119 de Cancérologie et Expérimentales. Marseille
1988-1990: Visiting scientist - Division of Molecular and Developmental Biology (A. Bernstein). Mount Sinaï Hospital, Toronto, Canada (MRC Fellowship)
1997 Visiting Scientist fellowship INSERM/MRC, Ontario Cancer Institute Dr. R Rottapel, Toronto, Canada
Expert activities
Vice-president of the Club Hématopoièse et Oncogenèse (1995-97), secretary (1997-99), vice president (2005->2008)
Member of the SFH administration board (Société Française d’Hématologie) 1999-> 2002
Member of the Scientific board of AFIRMM (Mastocytosis patient consortium) since 1999
Expert of the national expertise committee of LIGUE Régionale, Ile de France, 2001-2004
Expert of the national expertise committee of ARC 2000-2005
Expert of the national expertise committee of LNCC 2001-2005 then in 2011-2013
President of the national expertise committee of ARC CN4 and member of the scientific committee
Grants
Team Label Ligue since 2001
Supported by OSEO, Inca and FRM
The laboratory is recognized by the French Health Ministry as reference center for Mastocytosis study (CEREMAST)
Other activity
Cofounder of AB Science Company (Paris) France
Member of the AB Science Scientific Committee
Team "Signalling, Hematopoiesis and Mechanism of Oncogenesis"
Hematopoiesis is a perfect model of cellular differentiation to study molecular mechanisms involved in the transition between a highly regulated system leading to differentiation programs and homeostasis to deregulated situations leading to proliferative syndromes and leukaemia. Our group contributes to the identification of mechanisms, transduction pathways and protein effectors initiated by genetic alterations affecting the c-Kit tyrosine kinase receptor. We identified these alterations in blood disorders, mastocytosis, gastrointestinal tumors and melanomas. Ultimately our goal is to generalize our strategy to study other receptors important in onco-hematology such as FLT3. Our project is based on three main approaches in which we have a recognized expertise :