TY - JOUR
T1 - Metabolic effects of antiangiogenic drugs in tumors
T2 - Therapeutic implications
AU - Quintieri, Luigi
AU - Selmy, Mohamed
AU - Indraccolo, Stefano
PY - 2014/5/15
Y1 - 2014/5/15
N2 - Antiangiogenic therapy has become a mainstay of cancer therapeutics, but clinical responses are generally short-term owing to the development of secondary resistance. Tumor starvation by antiangiogenic drugs is largely attributed to increased hypoxia and impaired nutrients supply, suggesting that angiogenesis inhibition causes remarkable metabolic perturbations in the tumor microenvironment. We review here recent acquisitions concerning metabolic effects of angiogenesis blockade in tumors and discuss the possibility that some metabolic features of tumor cells - i.e. their dependency from glucose as primary energy substrate - might affect tumor responses to anti-vascular endothelial growth factor treatment. Moreover, we discuss the hypothesis that anti-angiogenic therapy might foster metabolic evolution of tumors. The therapeutic implications of this hypothesis will be discussed further here.
AB - Antiangiogenic therapy has become a mainstay of cancer therapeutics, but clinical responses are generally short-term owing to the development of secondary resistance. Tumor starvation by antiangiogenic drugs is largely attributed to increased hypoxia and impaired nutrients supply, suggesting that angiogenesis inhibition causes remarkable metabolic perturbations in the tumor microenvironment. We review here recent acquisitions concerning metabolic effects of angiogenesis blockade in tumors and discuss the possibility that some metabolic features of tumor cells - i.e. their dependency from glucose as primary energy substrate - might affect tumor responses to anti-vascular endothelial growth factor treatment. Moreover, we discuss the hypothesis that anti-angiogenic therapy might foster metabolic evolution of tumors. The therapeutic implications of this hypothesis will be discussed further here.
KW - Angiogenesis
KW - Antiangiogenic therapy
KW - Glycolysis
KW - Metabolism
KW - VEGF
UR - http://www.scopus.com/inward/record.url?scp=84899416850&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84899416850&partnerID=8YFLogxK
U2 - 10.1016/j.bcp.2014.02.018
DO - 10.1016/j.bcp.2014.02.018
M3 - Article
C2 - 24607274
AN - SCOPUS:84899416850
VL - 89
SP - 162
EP - 170
JO - Biochemical Pharmacology
JF - Biochemical Pharmacology
SN - 0006-2952
IS - 2
ER -