High-fructose corn syrup enhances intestinal tumor growth in mice.

TitleHigh-fructose corn syrup enhances intestinal tumor growth in mice.
Publication TypeJournal Article
Year of Publication2019
AuthorsGoncalves MD, Lu C, Tutnauer J, Hartman TE, Hwang S-K, Murphy CJ, Pauli C, Morris R, Taylor S, Bosch K, Yang S, Wang Y, Van Riper J, H Lekaye C, Roper J, Kim Y, Chen Q, Gross SS, Rhee KY, Cantley LC, Yun J
JournalScience
Volume363
Issue6433
Pagination1345-1349
Date Published2019 03 22
ISSN1095-9203
KeywordsAdenomatous Polyposis Coli Protein, Animals, Carcinogenesis, Diet, High Fructose Corn Syrup, Intestinal Neoplasms, Mice, Mice, Mutant Strains, Neoplasm Grading, Tumor Burden
Abstract

Excessive consumption of beverages sweetened with high-fructose corn syrup (HFCS) is associated with obesity and with an increased risk of colorectal cancer. Whether HFCS contributes directly to tumorigenesis is unclear. We investigated the effects of daily oral administration of HFCS in adenomatous polyposis coli (APC) mutant mice, which are predisposed to develop intestinal tumors. The HFCS-treated mice showed a substantial increase in tumor size and tumor grade in the absence of obesity and metabolic syndrome. HFCS increased the concentrations of fructose and glucose in the intestinal lumen and serum, respectively, and the tumors transported both sugars. Within the tumors, fructose was converted to fructose-1-phosphate, leading to activation of glycolysis and increased synthesis of fatty acids that support tumor growth. These mouse studies support the hypothesis that the combination of dietary glucose and fructose, even at a moderate dose, can enhance tumorigenesis.

DOI10.1126/science.aat8515
Alternate JournalScience
PubMed ID30898933
PubMed Central IDPMC6487857
Grant ListK22 CA216036 / CA / NCI NIH HHS / United States
T32 AI007640 / AI / NIAID NIH HHS / United States
R01 NS093872 / NS / NINDS NIH HHS / United States
K08 CA230318 / CA / NCI NIH HHS / United States
P30 CA008748 / CA / NCI NIH HHS / United States
R35 CA197588 / CA / NCI NIH HHS / United States
P01 HD067244 / HD / NICHD NIH HHS / United States