Toward an effective strategy in glioblastoma treatment. Part I: resistance mechanisms and strategies to overcome resistance of glioblastoma to temozolomide.


Autoria(s): Messaoudi, Khaled; Clavreul, Anne; Lagarce, Frédéric
Contribuinte(s)

Micro et nanomédecines biomimétiques (MINT) ; Université d'Angers (UA) - Institut National de la Santé et de la Recherche Médicale (INSERM)

Centre Hospitalier Universitaire d'Angers (CHU Angers) ; PRES Université Nantes Angers Le Mans [UNAM]

Data(s)

2015

Resumo

International audience

<p>Glioblastoma multiforme (GBM) is a devastating disease and the most lethal of adult brain tumors. Treatment is based on surgery, radiotherapy and chemotherapy by oral temozolomide (TMZ), which is the most potent chemotherapy agent for the treatment of GBM. Despite TMZ efficiency, the prognosis of these tumors remains poor. This is because of inherent or acquired resistance of glioma tumor cells to TMZ. This resistance is caused by DNA repair enzyme activity, overexpression of epidermal growth factor receptor (EGFR), galectin-1, murine double minute 2 (Mdm2), p53 and phosphatase and tensin homolog (PTEN) mutations. Many strategies to overcome this resistance have been developed. In this review, we will describe the main mechanisms of GBM resistance to TMZ and different strategies developed to reverse the phenotype of these tumor cells. Finally, we will discuss the drawbacks and limitations of these strategies.</p>

Identificador

hal-01392441

https://hal.archives-ouvertes.fr/hal-01392441

DOI : 10.1016/j.drudis.2015.02.011

OKINA : ua10638

Idioma(s)

en

Publicador

HAL CCSD

Relação

info:eu-repo/semantics/altIdentifier/doi/10.1016/j.drudis.2015.02.011

Fonte

ISSN: 1878-5832

Drug Discov Today

https://hal.archives-ouvertes.fr/hal-01392441

Drug Discov Today, 2015, 20 (7), pp.899-905. <10.1016/j.drudis.2015.02.011>

Palavras-Chave #[SDV] Life Sciences [q-bio]
Tipo

info:eu-repo/semantics/article

Journal articles