Nattawan Suwannakul, Napat Armartmuntree, Raynoo Thanan, et al. Targeting fructose metabolism by glucose transporter 5 regulation in human cholangiocarcinoma. [J]. Genes & Diseases 9(6).(2022)
DOI:
Nattawan Suwannakul, Napat Armartmuntree, Raynoo Thanan, et al. Targeting fructose metabolism by glucose transporter 5 regulation in human cholangiocarcinoma. [J]. Genes & Diseases 9(6).(2022) DOI: 10.1016/j.gendis.2021.09.002.
Targeting fructose metabolism by glucose transporter 5 regulation in human cholangiocarcinoma
摘要
Abstract
lterations in cellular metabolism may contribute to tumor proliferation and survival. Upregulation of the facilitative glucose transporter (GLUT) plays a key role in promoting cancer. GLUT5 mediates modulation of fructose utilization
and its overexpression has been associated with poor prognosis in several cancers. However
its metabolic regulation remains poorly understood. Here
we demonstrated elevated GLUT5 expression in human cholangiocarcinoma (CCA)
using RNA sequencing data from samples of human tissues and cell lines
as compared to normal liver tissues or a cholangiocyte cell line. Cells exhibiting high-expression of GLUT5 showed increased rates of cell proliferation and ATP production
particularly in a fructose-supplemented medium. In contrast
GLUT5 silencing attenuated cell proliferation
ATP production
cell migration/invasion
and improved epithelial–mesenchymal transition (EMT) balance. Correspondingly
fructose consumption increased tumor growth in a nude mouse xenograft model
and GLUT5 silencing suppressed growth
supporting the tumor-inhibitory effect of GLUT5 downregulation. Furthermore
in the metabolic pathways of fructolysis-Warburg effect
the expression levels of relative downstream genes
including ketohexokinase (KHK)
aldolase B (ALDOB)
lactate dehydrogenase A (LDHA)
and monocarboxylate transporter 4 (MCT4)
as well as hypoxia-inducible factor 1 alpha (HIF1A)
were altered in a GLUT5 expression-dependent manner. Taken together
these findings indicate that GLUT5 could be a potential target for CCA therapeutic approach via metabolic regulation.