A Ketogenic Diet in Combination with Gemcitabine Increases Survival in Pancreatic Cancer KPC Mice

Author:

Cortez Natalia E.1ORCID,Rodriguez Lanzi Cecilia1,Hong Brian V.1ORCID,Xu Jihao2ORCID,Wang Fangyi3ORCID,Chen Shuai4ORCID,Ramsey Jon J.5,Pontifex Matthew G.6,Müller Michael6ORCID,Vauzour David6ORCID,Vahmani Payam3ORCID,Hwang Chang-il27,Matsukuma Karen78,Mackenzie Gerardo G.17ORCID

Affiliation:

1. 1Department of Nutrition, University of California, Davis. Davis, California.

2. 2Department of Microbiology and Molecular Genetics, University of California Davis, Davis, California.

3. 3Department of Animal Science, University of California, Davis. Davis, California.

4. 4Division of Biostatistics, Department of public Health Sciences, University of California, Davis. Davis, California.

5. 5Department of Molecular Biosciences, University of California Davis, Davis, California.

6. 6Norwich Medical School, Biomedical Research Centre, University of East Anglia, Norwich, United Kingdom.

7. 7University of California, Davis Comprehensive Cancer Center, Sacramento, California.

8. 8Department of Pathology and Laboratory Medicine, Sacramento, California.

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 antitumor 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: 65% carb, 15% protein, 20% fat), a KD (%kcal: 1% carb, 15% protein, 84% 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 with mice fed a CD or CG. KPC mice fed a KG had a significant increase in overall median survival compared with KPC mice fed a CD (increased overall median survival by 42%). Interestingly, when the data were 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. Significance: This article is the first preclinical study to comprehensively evaluate the effect of a KD alongside chemotherapy using a standard autochthonous genetically modified mouse model (in both male and female KPC mice).

Funder

HHS | NIH | National Cancer Institute

USDA | National Institute of Food and Agriculture

Publisher

American Association for Cancer Research (AACR)

Reference51 articles.

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