Reference : Checkpoints modulation by the human T-lymphotropic virus type 1 (HTLV-1) Tax protein...
Scientific congresses and symposiums : Poster
Human health sciences : Oncology
http://hdl.handle.net/2268/137736
Checkpoints modulation by the human T-lymphotropic virus type 1 (HTLV-1) Tax protein : towards new therapeutic approaches
English
[en] Modulation des points de contrôle par la protéine Tax du virus T-lymphotrope humain de type 1 (HTLV-1) : vers une nouvelle approche thérapeutique
Carpentier, Alexandre mailto [Université de Liège - ULiège > Chimie et bio-industries > Biologie cell. et moléc. >]
Willems, Luc mailto []
22-Jun-2012
A0
No
No
National
GIGA Cancer Day
22/06/2012
Université de Liège (GIGA)
Liège
Belgique
[en] HTLV-1 ; Tax ; DDR
[en] HTLV-1 infects approximately 20 million people worldwide and causes several diseases. This virus is responsible for the adult T-cell leukemia (ATL) and for a chronic neuropathology (TSP/HAM). There is currently no satisfactory treatment for these diseases. Among the proteins encoded by HTLV-1, Tax appears to play an important role in the mechanisms leading to pathogenicity.
We are interested in the mechanisms of cell transformation by HTLV-1 and more particularly in the interplay between the viral Tax oncoprotein and the DNA damage response (DDR). We demonstrated that transient expression of Tax results in DNA damage, cell cycle arrest and activation of the ATM-Chk2-p53 axis of the DDR. In fibroblasts, cell cycle arrest occurs at the G1 and G2 phases depending on the p53 background. In contrast, HTLV-1 infected lymphocytes proliferate continuously and appear to be adapted to Chk2 and p53 checkpoints. This mechanism allows infected lymphocytes to proliferate despite the presence of genomic lesions. Our data shows that HTLV-1 infected cells use an alternative DNA repair pathway controlled by ATM and Chk1. This particularity may be used as novel therapeutic approach based on the principle of synthetic lethality.
Laboratoire de Biologie Moléculaire, Gembloux Agro-Bio Tech
Télévie; FNRS; Fondation contre le cancer
Thérapie de la leucémie à cellules T de l'adulte
Researchers ; Professionals ; Students
http://hdl.handle.net/2268/137736

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