Abstract：
:The invasive transformation of A-459 lung epithelial carcinoma cells has been linked to the autocrine regulation of malignant phenotypic changes by transforming growth factor beta (TGF-beta). Here we demonstrate, using stable 13C glucose isotopes, that the transformed phenotype is characterized by decreased CO2 production via direct glucose oxidation but increased nucleic acid ribose synthesis through the nonoxidative reactions of the pentose cycle. Increased nucleic acid synthesis through the nonoxidative pentose cycle imparts the metabolic adaptation of nontransformed cells to the invasive phenotype that potentially explains the fundamental metabolic disturbance in tumor cells: highly increased nucleic acid synthesis despite hypoxia and decreased glucose oxidation.
journal_name
Cancer Resjournal_title
Cancer researchauthors
Boros LG,Torday JS,Lim S,Bassilian S,Cascante M,Lee WNsubject
Has Abstractpub_date
2000-03-01 00:00:00pages
1183-5issue
5eissn
0008-5472issn
1538-7445journal_volume
60pub_type
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