SharePoint
Aide
Faire avancer la sûreté nucléaire

La Recherchev2

Publications

Molecular and cellular response of the most extensively used rodent glioma models to radiation and/or cisplatin


Fermer

Authentification

Email :

Mot de passe :

Titre de la revue : Journal of neuro-oncology Volume : 86 N° : 1 Pagination : 13-21 Date de publication : 01/01/2008

Type de document > *Article de revue

Mots clés >

Unité de recherche > IRSN/DRPH/SDE/LMDN

Auteurs > BALOSSO Jacques, BENCOKOVA Zuzana, DEVIC Clément, FORAY Nicolas, GASTALDO Jérome, JOUBERT Aurélie, MASSART Catherine, PAURON Laurianne

Date de publication > 01/01/2008

Résumé

Purpose: Anti-glioma strategies are generally based on trials involving rodent models whose choice remains based on proliferative capacity and availability. Recently, our group obtained the most protracted survival of rats bearing F98 gliomas by combining synchrotron X-rays and intracerebral cisplatin injection (Biston et al., Cancer. Res. 2004, 64, 2317-2323). The response to such treatment was suggested to be dependent on BRCA1, a tumour suppressor known to be involved in the response to radiation and cisplatin. In order to verify the impact of BRCA1 functionality upon success of anti-glioma trials, radiobiological features and BRCA1-dependent stress signaling were investigated in the most extensively used rodent glioma models. Methods: Cell death pathways, cell cycle arrests, DNA repair and stress signaling were evaluated in response to radiation and cisplatin in C6, 9L and F98 models. Results: Rodent glioma models showed a large spectrum of cellular radiation response. Surprisingly, BRCA1 was found to be functionally impaired in C6 and F98 favouring genomic instability, tumour heterogeneity and tolerance of unrepaired DNA damage. Significance: Our findings strengthened the importance of the choice of the glioma model on genetic and radiobiological bases, inasmuch as all these rat glioma models are induced by nitrosourea-mediated mutagenesis that may favour specific gene mutations. Particularly, BRCA1 status may condition the response to anti-glioma treatments. Furthermore, since BRCA1 acts as a tumour suppressor in a number of malignancies, our findings raise also the question of the implication of BRCA1 in brain tumours formation.