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Page de résumé pour ULgetd-04012009-102915

Auteur : Henkens, Rachel
E-mail de l'auteur : R.Henkens@student.ulg.ac.be
URN : ULgetd-04012009-102915
Langue : Français/French
Titre : Étude de l'expression, de la régulation et du rôle de la phosphatase à double spécificité VHR dans le cancer du col de l'utérus.
Intitulé du diplôme : Doctorat en sciences biomédicales et pharmaceutiques
Département : Médecine - Département des sciences précliniques
Jury :
Nom : Titre :
ALONSO, André Membre du jury/Committee Member
CHARIOT, Alain Membre du jury/Committee Member
DELVENNE, Philippe Membre du jury/Committee Member
GEENEN, Vincent Membre du jury/Committee Member
GIANNINI, Sandra Membre du jury/Committee Member
PIETTE, Jacques Président du jury/Committee Chair
MOUTSCHEN, Michel Promoteur/Director
RAHMOUNI, Souad Promoteur/Director
Mots-clés :
  • phosphatase
  • DUSP
  • cancer du col de l'utérus
  • VHR
Date de soutenance : 2009-04-30
Type d'accès : Restreint/Intranet
Résumé :

The proteins tyrosine kinases (PTKs) and the proteins tyrosine phosphatases (PTPs) are very important proteins implicated in the regulation of the cell cycle and numerous human diseases including cancer. VHR is a dual-specific phosphatase whose principles substrats are the MAPKs ERK and JNK. Previous studies of our laboratory showed that this phosphatase is regulated during the cell cycle. Its level is low during the G1 phase and increases during S and G2 phases to reach a top at the G2/M phases. The low level of VHR during the G1 phase is probably due to an alteration of the protein stability demonstrated by a decreased half-life (after treatment of the cell with cycloheximide). In addition, VHR deletion by RNA interference in HeLa cells induces a cell cycle arrest during G1/S and G2/M transitions [1].

In the first part of our work, we show that the dual-specificity phosphatase VHR is overexpressed in cervix cancer cell lines compared to primary keratinocytes. These cell lines are infected (HeLa, CaSki and SiHa) or not (C33 and HT3) by HPV, suggesting that VHR overexpression is HPV independent, virus which is responsible of cervix cancer. We show that VHR overexpression is associated with a differential subcellular localization. Indeed, VHR is localized in the cytoplasm of normal keratinocytes while it localizes in both cytoplasm and nucleus of the cell lines studied. This observed overexpression is not associated with an increased expression of its mRNA but with a stabilization of the protein. CHX chase showed us that VHR half life is about 2 hours in primary keratinocytes and longer than 8 hours in cervix cancer cell lines.

The TMA technique allowed us to study a large number of preneoplasic and neoplasic cervical lesions. Interestingly, we observe that VHR is significantly overexpressed in CIN III (Cervical intraepithelial Lesions III) (n=18) and in SCCs (Squamous Cell Carcinoma) (n=12) compared to normal exocols (n=16) and although in ADCs (Adenocarcinoma) (n=12) and AISs (Adenocarcinoma in situ) (n=9) compared to normal endocols (n=19). The differential subcellular localization is also observed in CIN III and SCCs compared to normal exocols but not in ADCs and AISs compared to normal endocols.

In the second part of our work, we analyzed the effect of small selectif inhibitors of VHR developped by Dr. L. Tautz from Burnham Institute in La Jolla, CA on cervical cell lines, HeLa and CaSki. We show that these small sulfonic acids induced a decreased number and a decreased proliferation of HeLa and CaSki cells. These effects are similar to those induced by RNA interference. We also show that these inhibitors induced an increased level of ERK phosphorylation. Since ERK is a specific substrat of VHR, these results suggest that the small inhibitors developped by L. Tautz et al. are specific for VHR.

Autre version :
Fichiers :
Nom du fichier Taille Temps de chargement évalué (HH:MI:SS)
Modem 56K ADSL
[Restreint/Intranet] Henkensetal.BMCCancer.pdf 1.52 Mb 00:03:37 00:00:08
[Restreint/Intranet] Rahmounietal.Nature.pdf 4.56 Mb 00:10:52 00:00:24
[Restreint/Intranet] TheseRachelHenkens.pdf 2.68 Mb 00:06:22 00:00:14
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