TY - JOUR
T1 - ROS homeostasis and metabolism
T2 - A critical liaison for cancer therapy
AU - Kim, Jaehong
AU - Kim, Jongdoo
AU - Bae, Jong Sup
N1 - Publisher Copyright:
© 2016 KSBMB. All rights reserved.
PY - 2016/11/4
Y1 - 2016/11/4
N2 - Evidence indicates that hypoxia and oxidative stress can control metabolic reprogramming of cancer cells and other cells in tumor microenvironments and that the reprogrammed metabolic pathways in cancer tissue can also alter the redox balance. Thus, important steps toward developing novel cancer therapy approaches would be to identify and modulate critical biochemical nodes that are deregulated in cancer metabolism and determine if the therapeutic efficiency can be influenced by changes in redox homeostasis in cancer tissues. In this review, we will explore the molecular mechanisms responsible for the metabolic reprogramming of tumor microenvironments, the functional modulation of which may disrupt the effects of or may be disrupted by redox homeostasis modulating cancer therapy.
AB - Evidence indicates that hypoxia and oxidative stress can control metabolic reprogramming of cancer cells and other cells in tumor microenvironments and that the reprogrammed metabolic pathways in cancer tissue can also alter the redox balance. Thus, important steps toward developing novel cancer therapy approaches would be to identify and modulate critical biochemical nodes that are deregulated in cancer metabolism and determine if the therapeutic efficiency can be influenced by changes in redox homeostasis in cancer tissues. In this review, we will explore the molecular mechanisms responsible for the metabolic reprogramming of tumor microenvironments, the functional modulation of which may disrupt the effects of or may be disrupted by redox homeostasis modulating cancer therapy.
UR - http://www.scopus.com/inward/record.url?scp=84994608607&partnerID=8YFLogxK
U2 - 10.1038/emm.2016.119
DO - 10.1038/emm.2016.119
M3 - Article
C2 - 27811934
AN - SCOPUS:84994608607
SN - 1226-3613
VL - 48
JO - Experimental and Molecular Medicine
JF - Experimental and Molecular Medicine
IS - 11
M1 - e269
ER -