Proteomics

Dataset Information

0

Human glioma cell-line proteomics upon treatment with different drugs


ABSTRACT: Increasing evidence suggests that induction of lethal autophagy carries potential significance for the treatment of glioblastoma (GBM). In continuation of our previous work, we investigated if autophagy-inducing compunds can trigger ATG-dependent cell death in human MZ-54 GBM cells and which pathways may be affected using TMT10-based quantitative proteomics as one of the tools.

INSTRUMENT(S): Q Exactive

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Brain

SUBMITTER: Georg Tascher  

LAB HEAD: Christian Münch

PROVIDER: PXD015074 | Pride | 2021-02-26

REPOSITORIES: Pride

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Publications

Autophagy activation, lipotoxicity and lysosomal membrane permeabilization synergize to promote pimozide- and loperamide-induced glioma cell death.

Meyer Nina N   Henkel Lisa L   Linder Benedikt B   Zielke Svenja S   Tascher Georg G   Trautmann Sandra S   Geisslinger Gerd G   Münch Christian C   Fulda Simone S   Tegeder Irmgard I   Kögel Donat D  

Autophagy 20210119 11


Increasing evidence suggests that induction of lethal macroautophagy/autophagy carries potential significance for the treatment of glioblastoma (GBM). In continuation of previous work, we demonstrate that pimozide and loperamide trigger an ATG5- and ATG7 (autophagy related 5 and 7)-dependent type of cell death that is significantly reduced with cathepsin inhibitors and the lipid reactive oxygen species (ROS) scavenger α-tocopherol in MZ-54 GBM cells. Global proteomic analysis after treatment wit  ...[more]

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