학술논문

A ketogenic diet in combination with gemcitabine increases survival in pancreatic cancer KPC mice
Document Type
article
Source
Cancer Research Communications. 2(9)
Subject
Biomedical and Clinical Sciences
Oncology and Carcinogenesis
Rare Diseases
Complementary and Integrative Health
Digestive Diseases
Pancreatic Cancer
Cancer
Nutrition
Mice
Male
Female
Animals
Gemcitabine
Diet
Ketogenic
Pancreatic Neoplasms
Carcinoma
Pancreatic Ductal
ERK and AKT signaling pathways
Ketogenic diet
Lipid metabolism
gemcitabine
microbiome
pancreatic cancer
pancreatic ductal adenocarcinoma
Language
Abstract
Pancreatic ductal adenocarcinoma (PDAC) continues to be a major health problem. A ketogenic diet (KD), characterized by a very low carbohydrate and high fat composition, has gained attention for its anti-tumor potential. We evaluated the effect and mechanisms of feeding a strict KD alone or in combination with gemcitabine in the autochthonous LSL-KrasG12D/+; LSL-Trp53 R172H/+; Pdx1-Cre (KPC) mouse model. For this purpose, both male and female pancreatic tumor-bearing KPC mice were allocated to a control diet (CD; %kcal: 70% carb, 14% protein, 16% fat), a KD (%kcal: 14% protein, 1% carb, 85% fat), a CD + gemcitabine (CG), or a KD + gemcitabine (KG) group. Mice fed a KD alone or in combination with gemcitabine showed significantly increased blood β-hydroxybutyrate levels compared to mice fed a CD or CG. KPC mice fed a KG had a significant increase in overall median survival compared to KPC mice fed a CD (increased overall median survival by 42%). Interestingly, when the data was disaggregated by sex, the effect of a KG was significant in female KPC mice (60% increase in median overall survival), but not in male KPC mice (28% increase in median overall survival). Mechanistically, the enhanced survival response to a KD combined with gemcitabine was multifactorial, including inhibition of ERK and AKT pathways, regulation of fatty acid metabolism and the modulation of the gut microbiota. In summary, a KD in combination with gemcitabine appears beneficial as a treatment strategy in PDAC in KPC mice, deserving further clinical evaluation.