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BCL2 expression in CD105 positive neoangiogenic cells and tumor progression in angioimmunoblastic T-cell lymphoma.
Ratajczak P., Leboeuf C., Wang L., Brière J., Loisel-Ferreira I., Thiéblemont C., Zhao W.-L., Janin A.
Modern Pathology 25, 6 (2012) 805-14 - http://www.hal.inserm.fr/inserm-00682931
 (22322190) 
BCL2 expression in CD105 positive neoangiogenic cells and tumor progression in angioimmunoblastic T-cell lymphoma.
Philippe Ratajczak () 1, Christophe Leboeuf1, Li Wang1, 2, Josette Brière1, 3, Irmine Loisel-Ferreira1, Catherine Thiéblemont1, 4, Wei-Li Zhao1, 2, Anne Janin1, 3
1 :  Gvh et Gvl : Physiopathologie Chez l'Homme et Chez l'Animal, Incidence et Role Therapeutique
INSERM : U728 – Université Paris VII - Paris Diderot
Hopital Saint-Louis - Centre Hayem PARIS VII 1, Avenue Claude Vellefaux 75475 PARIS CEDEX 10
France
2 :  Laboratory of Pathogenesis of Leukemia
Shanghai Rui Jin Hospital – Shanghai Jiao Tong University School of Medicine – Shanghai Institute for Biological Sciences Chinese Academy of Sciences
225 South Chongqing Road - Shanghai 200025
Chine
3 :  Service d'anatomo-pathologie
Assistance publique - Hôpitaux de Paris (AP-HP) – Hôpital Saint-Louis – Université Paris VII - Paris Diderot
1 avenue Claude Vellefaux 75475 Paris cedex 10
France
4 :  Service d'hématologie-oncologie adultes
Assistance publique - Hôpitaux de Paris (AP-HP) – Hôpital Saint-Louis – Université Paris VII - Paris Diderot
1, avenue Claude-Vellefaux 75475 PARIS Cedex 10
France
The angiogenic microenvironment has been known to be a component of angioimmunoblastic T-cell lymphoma since its initial characterization. We have shown that angioimmunoblastic T-cell lymphoma endothelial cells produce vascular endothelial growth factor-A (VEGFA), and participate in lymphoma progression. In squamous cell carcinoma, endothelial BCL2 expression induces a crosstalk with tumor cells through VEGFA, a major mediator of tumoral angiogenesis. In the present study, we analyzed BCL2 and VEGFA in 30 angioimmunoblastic T-cell lymphomas, using triple immunofluorescence to identify protein coexpression in well-characterized lymphoma cells and microenvironment neoangiogenic endothelial cells. Using quantitative real-time PCR, we assessed mRNA expression levels in laser-microdissected endothelial and lymphoma cells. In lymphoma cells, as in endothelial cells, BCL2 and VEGFA proteins were coexpressed. BCL2 was expressed only in neoangiogenic CD34(+)CD105(+) endothelial cells. In laser-microdissected cells, mRNA studies showed a significant relationship between BCL2 and VEGFA levels in CD34(+) endothelial cells, but not in CD3(+)CD10(+)lymphoma cells, or in CD34(+) endothelial cells from lymph node hyperplasia. Further study showed that, in AITL, BCL2 mRNA levels in CD34(+)CD105(+) neoangiogenic endothelial cells also correlated with microvessel density, International Prognostic Index, Ann Arbor stage, bone marrow involvement and elevated LDH. BCL2 expression by CD105(+) neoangiogenic endothelial cells is related to tumor progression in angioimmunoblastic T-cell lymphoma.
Sciences du Vivant/Cancérologie
Anglais
0893-3952

Articles dans des revues avec comité de lecture
10.1038/modpathol.2012.1
Modern Pathology (Mod Pathol)
Publisher Nature Publishing Group: Open Access Hybrid Model Option B
ISSN 0893-3952 (eISSN : 1530-0285)
internationale
06/2012
10/02/2012
25
6
805-14

Angioimmunolbastic T-Cell Lyphoma – BCL2 – CD105 – endothelial cell – neoangiogenesis – VEGF
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