Effects of HIF-1 and HIF2 on Growth and Metabolism of Clear-Cell Renal Cell Carcinoma 786-0 Xenografts
Author(s) -
Swethajit Biswas,
Helen Troy,
Russell Leek,
YuenLi Chung,
Jiliang Li,
Raju R. Raval,
Helen Turley,
Kevin C. Gatter,
Francesco Pezzella,
John R. Griffiths,
Marion Stubbs,
Adrian L. Harris
Publication year - 2010
Publication title -
journal of oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.228
H-Index - 54
eISSN - 1687-8469
pISSN - 1687-8450
DOI - 10.1155/2010/757908
Subject(s) - cell growth , glycolysis , lactate dehydrogenase , cancer research , apoptosis , clear cell renal cell carcinoma , pyruvate kinase , in vivo , medicine , anaerobic glycolysis , cell , warburg effect , metabolite , metabolism , renal cell carcinoma , endocrinology , biology , biochemistry , enzyme , microbiology and biotechnology
In cultured clear-cell renal carcinoma (CCRCC) 786-0 cells transfected with HIF1 α (HIF-1+), HIF-2 α (HIF-2+), or empty vector (EV), no significant differences were observed in the growth rates in vitro , but when grown in vivo as xenografts HIF-2 α significantly increased, and HIF-1 α significantly decreased growth rates, compared to EV tumors. Factors associated with proliferation were increased and factors associated with cell death were decreased in HIF-2+ tumors. Metabolite profiles showed higher glucose and lower lactate and alanine levels in the HIF-2+ tumors whilst immunostaining demonstrated higher pyruvate dehydrogenase and lower pyruvate dehydrogenase kinase 1, compared to control tumors. Taken together, these results suggest that overexpression of HIF-2 α in CCRCC 786-0 tumors regulated growth both by maintaining a low level of glycolysis and by allowing more mitochondrial metabolism and tolerance to ROS induced DNA damage. The growth profiles observed may be mediated by adaptive changes to a more oxidative phenotype.
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