TY - JOUR
T1 - Novel ways to target brain tumour metabolism
AU - Stieber, Daniel
AU - Abdul Rahim, Siti A.
AU - Niclou, Simone P.
N1 - Funding Information:
The authors declare no conflict of interest. The authors acknowledge the financial support of the Fonds National de la Recherche (FNR) of Luxembourg and of the Centre de la Recherche Public de la Santé (CRP-Santé) in Luxembourg.
PY - 2011/10
Y1 - 2011/10
N2 - Introduction: Glioblastoma remains a highly aggressive primary brain cancer with very poor prognosis. The detection of mutations in the metabolic enzyme isocitrate dehydrogenase in gliomas, has broadened our view of tumourigenic mechanisms. Together with renewed awareness of tumour-specific energy metabolism, research is pointed towards novel ways for targeting brain cancer. Areas covered: This paper reviews recent knowledge on the possible tumourigenic mechanism of mutant isocitrate dehydrogenase, and provides a detailed overview of cancer-specific metabolic enzymes associated with glycolysis and intracellular pH regulation. It also discusses available drugs that may serve as a basis for novel drug development to target metabolic transformation in gliomas. Expert opinion: Despite the fact that energy metabolism is a very basic cellular process, tumour specific alterations in key metabolic processes represent promising targets for glioma treatment. Novel therapies against gliomas, including those that target metabolic transformation, need to consider the genetic background of the individual tumours, to allow the correlation of treatment response with the underlying biological status, both in preclinical and clinical studies.
AB - Introduction: Glioblastoma remains a highly aggressive primary brain cancer with very poor prognosis. The detection of mutations in the metabolic enzyme isocitrate dehydrogenase in gliomas, has broadened our view of tumourigenic mechanisms. Together with renewed awareness of tumour-specific energy metabolism, research is pointed towards novel ways for targeting brain cancer. Areas covered: This paper reviews recent knowledge on the possible tumourigenic mechanism of mutant isocitrate dehydrogenase, and provides a detailed overview of cancer-specific metabolic enzymes associated with glycolysis and intracellular pH regulation. It also discusses available drugs that may serve as a basis for novel drug development to target metabolic transformation in gliomas. Expert opinion: Despite the fact that energy metabolism is a very basic cellular process, tumour specific alterations in key metabolic processes represent promising targets for glioma treatment. Novel therapies against gliomas, including those that target metabolic transformation, need to consider the genetic background of the individual tumours, to allow the correlation of treatment response with the underlying biological status, both in preclinical and clinical studies.
KW - IDH
KW - PH regulation
KW - glioblastoma
KW - gliomas
KW - glycolysis
KW - hypoxia
KW - metabolic transformation
KW - metabolism
KW - personalized medicine
UR - http://www.scopus.com/inward/record.url?scp=80052902545&partnerID=8YFLogxK
UR - https://www.ncbi.nlm.nih.gov/pubmed/21635150
U2 - 10.1517/14728222.2011.588211
DO - 10.1517/14728222.2011.588211
M3 - Review article
C2 - 21635150
AN - SCOPUS:80052902545
SN - 1472-8222
VL - 15
SP - 1227
EP - 1239
JO - Expert Opinion on Therapeutic Targets
JF - Expert Opinion on Therapeutic Targets
IS - 10
ER -