- Oral presentation
- Open Access
Can inhibiting insulin/IGF signaling with dietary carbohydrate restriction play a role in treatment/prevention of cancers?
Cancer & Metabolismvolume 2, Article number: O31 (2014)
Hyperinsulinemia, hyperglycemia, and obesity have been identified as risk factors for a variety of cancers . Insulin inhibition (INSINH) can potentially limit cancer growth by factors including ketosis , and apoptosis secondary to fatty acid synthase inhibition  as well as intracellular potassium depletion . Furthermore, dysregulation of many signaling proteins downstream of the insulin/IGF receptors such as PI3K/Akt, mTOR (inhibition) and AMPK (amplification) is a major area of drug target development [5, 6]. We performed a four week INSINH diet in patients with advanced cancers to study safety/feasibility and also to examine a change in18F-2-fluoro, 2-deoxyglucose (FDG) uptake on PET scan as a surrogate measure for tumor response.
Eligible patients had failed or refused ≥2 standard chemotherapy courses. Exclusions included concurrent chemotherapy, end-organ disease, hypoglycemic medications, difficult compliance, or BMI < 20. A supervised INSINH diet restricted starches and sugars for 28 days, and was monitored weekly for macronutrient intake, body weight, [glucose] [BHB], [insulin], [IGF1,2]. An exit four-week PET was obtained for comparison with the baseline scan.
Ten subjects with diverse cancers completed ≥ 26 days of INSINH without associated unsafe adverse effects. Mean caloric intake decreased (35 ± 6) % vs. predicted requirements despite our best efforts to encourage increased food consumption. Weight loss (median 4%, range 0.0-6.1%) was not judged a health risk in any subject. Mild, reversible side effects included constipation (n=2), transient fatigue (n=5), and leg cramps (n=2). Among nine patients with pre-trial progressive disease (PD) five demonstrated post-trial stable disease or partial remission (SD/ PR) on PET. SD/PR correlated with three-fold higher ketosis compared to those with continued PD (n=4), (p<0.02), but was uncorrelated with reduced calorie intake (p=0.45) or weight loss (p=0.81). Insulin correlated inversely with ketosis (r=0.62, p=0.026), but did not correlate with IFG(1 or 2).
Preliminary pilot data in ten subjects demonstrated that an INSINH diet is safe and feasible in selected patients with advanced cancer. The extent of ketosis, but neither calorie deficit nor weight loss correlated with SD/PR. The small sample size requires further study. Further exploration is also required to evaluate an insulin inhibiting diet’s: 1. mechanism in relation to calorie restriction; 2. role as an adjunct to metabolic or cytotoxic therapies; 3. long-term value to reduce overall cancer risk.
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This work was supported by the State University of New York Research Foundation and the Robert and Veronica Atkins Foundation. This publication also was supported in part by CTSA grants UL1RR025750, KL2RR025749 (gs4), and TL1RR025748 from the National Center for Research Resources, a component of the National Institutes of Health, and the National Institutesof Health Roadmap for Medical Research.