Glioblastoma, hypoxia and autophagy: a survival-prone ‘ménage-à-trois’

Archive ouverte

Jawhari, Soha | Ratinaud, Marie-Hélène | Verdier, Mireille

Edité par CCSD ; Nature Publishing Group -

International audience. Glioblastoma multiforme is the most common and the most aggressive primary brain tumor. It is characterized by a high degree of hypoxia and also by a remarkable resistance to therapy because of its adaptation capabilities that include autophagy. This degradation process allows the recycling of cellular components, leading to the formation of metabolic precursors and production of adenosine triphosphate. Hypoxia can induce autophagy through the activation of several autophagy-related proteins such as BNIP3, AMPK, REDD1, PML, and the unfolded protein response-related transcription factors ATF4 and CHOP. This review summarizes the most recent data about induction of autophagy under hypoxic condition and the role of autophagy in glioblastoma.

Suggestions

Du même auteur

Autophagy and TrkC/NT-3 signaling joined forces boost the hypoxic glioblastoma cell survival

Archive ouverte | Jawhari, Soha | CCSD

International audience

Autophagy takes place in mutated p53 neuroblastoma cells in response to hypoxia mimetic CoCl(2).

Archive ouverte | Naves, Thomas | CCSD

International audience. Solid tumors like neuroblastoma exhibit hypoxic areas, which can lead both to cell death or aggressiveness increase. Hypoxia is a known stress able to induce stabilization of p53, implicated ...

Autophagic subpopulation sorting by sedimentation field-flow fractionation.

Archive ouverte | Naves, Thomas | CCSD

International audience. The development of hypoxic areas often takes place in solid tumors and leads cells to undergo adaptive signalization like autophagy. This process is responsible for misfolded or aggregated pr...

Chargement des enrichissements...