Abstract
Pancreatic cancer is the third leading cause of cancer-related death in the United States. Current chemotherapy options provide limited benefits. Emerging evidence suggests that a ketogenic diet (KD) exerts anti-tumor effects by reprogramming tumor metabolism and revealing therapeutic vulnerabilities. Efforts to target glutamine metabolism—an essential pathway in many cancers—have shown promise in preclinical models, but clinical efficacy has remained limited. Here, we show that a KD increases tricarboxylic acid (TCA) cycle activity and elevates reliance on glutamine-related metabolites in murine pancreatic cancer models and in vitro under KD-mimicking conditions. This metabolic adaptation occurs in response to reduced glucose availability. We demonstrate that combining glutamine metabolism inhibitors, such as CB-839 or 6-diazo-5-oxo-L-norleucine (DON), with a KD leads to robust anti-tumor effects in preclinical models of pancreatic cancer. Thus, metabolic vulnerability induced by dietary intervention provides a rationale for combining glutamine-targeted therapies with a ketogenic diet in future clinical studies.
| Original language | English (US) |
|---|---|
| Article number | 102770 |
| Journal | Cell Reports Medicine |
| Volume | 7 |
| Issue number | 5 |
| DOIs | |
| State | Published - May 19 2026 |
All Science Journal Classification (ASJC) codes
- General Medicine
- General Biochemistry, Genetics and Molecular Biology
Keywords
- PDAC nutrient flux
- chemotherapy
- combination therapy
- glutamine metabolism
- glutamine tracing
- ketogenic diet
- ketogenic diet media
- pancreatic cancer
- targeted therapy
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