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New biomarkers in T-cell lymphomas.
Bisig B., Gaulard P., De Leval L.
Best Practice and Research: Clinical Haematology 25, 1 (2012) 13-28 - http://www.hal.inserm.fr/inserm-00693167
(22409820)
New biomarkers in T-cell lymphomas.
Bettina Bisig1, 2, Philippe Gaulard3, 4, Laurence De Leval () 1, 2, 5
1 :  Department of Pathology
Centre Hospitalier Universitaire Sart Tilman
Liège
Belgique
2 :  Laboratory of Experimental Pathology
Université de Liège
Groupe Interdisciplinaire de Génoprotéomique Appliquée (GIGA) - Research
Belgique
3 :  Institut Mondor de Recherche Biomédicale
INSERM : U955 – Université Paris-Est Créteil Val-de-Marne (UPEC) – IFR10
8 rue du Général Sarrail, 94010 Créteil
France
4 :  Service d'anatomie et cytologie pathologiques [Mondor]
Assistance publique - Hôpitaux de Paris (AP-HP) – Hôpital Henri Mondor – Université Paris-Est Créteil Val-de-Marne (UPEC)
51 Av Maréchal de Lattre de Tassigny, 94000 Créteil
France
5 :  Institute de Pathologie
Centre Hospitalier Universitaire Vaudois – Université de Lausanne
1011 Lausanne
Suisse
Peripheral T-cell lymphomas (PTCLs) are heterogeneous and uncommon malignancies characterized by an aggressive clinical course and a mostly poor outcome with current treatment strategies. The recent genome-wide molecular characterization of several entities has provided novel insights into their pathobiology and led to the identification of new biomarkers with diagnostic, prognostic or therapeutic implications for PTCL patients. Cell lineage and differentiation antigens (markers of γδ or NK lineage, of cytotoxicity, of follicular helper T cells) reflect the tumour's biological behaviour, and their detection in tissue samples may refine the diagnostic and prognostic stratification of the patients. Previously unrecognized gene rearrangements are being discovered (ITK-SYK translocation, IRF4/MUM1 and DUSP22 rearrangements), and may serve as diagnostic genetic markers. Deregulated molecules within oncogenic pathways (NF-κB, Syk, PDGFRα) and immunoreactive cell-surface antigens (CD30, CD52) have been brought to the fore as potential targets for guiding the development of novel therapies.
Sciences du Vivant/Biochimie, Biologie Moléculaire
Anglais
1532-1924

Articles dans des revues avec comité de lecture
10.1016/j.beha.2012.01.004
Best Practice and Research: Clinical Haematology (Best Pract Res Clin Haematol)
Publisher Elsevier
ISSN 1521-6926 
internationale
03/2012
07/02/2012
25
1
13-28

peripheral T-cell lymphomas – biomarkers – translocations – gene expression profiling – targeted therapy – prognosis
This work was supported by the Belgian National Fund for Scientific Research (Fonds de la Recherche Scientifique, FNRS), the Belgian Cancer Plan, and the French Foundation for Medical Research (Fondation pour la Recherche Médicale, FRM). Bettina Bisig and Laurence de Leval are a Scientific Research Worker-Télévie and a Senior Research Associate of the FNRS, respectively.
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Bisig-Gaulard-deLeval_BestPractResClinHaematol2012_Review_T-cell_lymphomas.doc(850.5 KB)
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