TY  - JOUR
AU  - Koch, Katharina
AU  - Hartmann, Rudolf
AU  - Schröter, Friederike
AU  - Kora Suwala, Abigail
AU  - Maciaczyk, Donata
AU  - Caroline Krüger, Andrea
AU  - Willbold, Dieter
AU  - Dietrich Kahlert, Ulf
AU  - Maciaczyk, Jaroslaw
TI  - Reciprocal regulation of the cholinic phenotype and epithelial-mesenchymal transition in glioblastoma cells
JO  - OncoTarget
VL  - 7
IS  - 45
SN  - 1949-2553
CY  - [S.l.]
PB  - Impact Journals LLC
M1  - FZJ-2016-05400
SP  - 73414-73431
PY  - 2016
AB  - Glioblastoma (GBM) is the most malignant brain tumor with very limited therapeutic options. Standard multimodal treatments, including surgical resection and combined radio-chemotherapy do not target the most aggressive subtype of glioma cells, brain tumor stem cells (BTSCs). BTSCs are thought to be responsible for tumor initiation, progression, and relapse. Furthermore, they have been associated with the expression of mesenchymal features as a result of epithelial-mesenchymal transition (EMT) thereby inducing tumor dissemination and chemo resistance. Using high resolution proton nuclear magnetic resonance spectroscopy (1H NMR) on GBM cell cultures we provide evidence that the expression of well-known EMT activators of the ZEB, TWIST and SNAI families and EMT target genes N-cadherin and VIMENTIN is associated with aberrant choline metabolism. The cholinic phenotype is characterized by high intracellular levels of phosphocholine and total choline derivatives and was associated with malignancy in various cancers. Both genetic and pharmacological inhibition of the cardinal choline metabolism regulator choline kinase alpha (CHKα) significantly reduces the cell viability, invasiveness, clonogenicity, and expression of EMT associated genes in GBM cells. Moreover, in some cell lines synergetic cytotoxic effects were observed when combining the standard of care chemotherapeutic temozolomide with the CHKα inhibitor V-11-0711. Taken together, specific inhibition of the enzymatic activity of CHKα is a powerful strategy to suppress EMT which opens the possibility to target chemo-resistant BTSCs through impairing their mesenchymal transdifferentiation. Moreover, the newly identified EMT-oncometabolic network may be helpful to monitor the invasive properties of glioblastomas and the success of anti-EMT therapy.
LB  - PUB:(DE-HGF)16
UR  - <Go to ISI:>//WOS:000387452100075
DO  - DOI:10.18632/oncotarget.12337
UR  - https://juser.fz-juelich.de/record/819805
ER  -