| Literature DB >> 30898933 |
Marcus D Goncalves1,2, Changyuan Lu3, Jordan Tutnauer1, Travis E Hartman4, Seo-Kyoung Hwang1, Charles J Murphy1,5, Chantal Pauli6, Roxanne Morris4, Sam Taylor1, Kaitlyn Bosch7, Sukjin Yang8, Yumei Wang8, Justin Van Riper8, H Carl Lekaye9, Jatin Roper10, Young Kim11, Qiuying Chen3, Steven S Gross3, Kyu Y Rhee4, Lewis C Cantley12, Jihye Yun13.
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.Entities:
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Year: 2019 PMID: 30898933 PMCID: PMC6487857 DOI: 10.1126/science.aat8515
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728