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Oncogenesis. 2016 Feb 15;5:e193. doi: 10.1038/oncsis.2016.2.

Dietary and pharmacological modification of the insulin/IGF-1 system: exploiting the full repertoire against cancer.

Oncogenesis

R J Klement, M K Fink

Affiliations

  1. Department of Radiation Oncology, Leopoldina Hospital Schweinfurt, Schweinfurt, Germany.
  2. Onkologische Praxis, Fürth, Germany.

PMID: 26878387 PMCID: PMC5154349 DOI: 10.1038/oncsis.2016.2

Abstract

As more and more links between cancer and metabolism are discovered, new approaches to treat cancer using these mechanisms are considered. Dietary restriction of either calories or macronutrients has shown great potential in animal studies to both reduce the incidence and growth of cancer, and to act synergistically with other treatment strategies. These studies have also shown that dietary restriction simultaneously targets many of the molecular pathways that are targeted individually by anticancer drugs. The insulin/insulin-like growth factor-1 (IGF-1) system has thereby emerged as a key regulator of cancer growth pathways. Although lowering of insulin levels with diet or drugs such as metformin and diazoxide seems generally beneficial, some practitioners also utilize strategic elevations of insulin levels in combination with chemotherapeutic drugs. This indicates a broad spectrum of possibilities for modulating the insulin/IGF-1 system in cancer treatment. With a specific focus on dietary restriction, insulin administration and the insulin-lowering drug diazoxide, such modifications of the insulin/IGF-1 system are the topic of this review. Although preclinical data are promising, we point out that insulin regulation and the metabolic response to a certain diet often differ between mice and humans. Thus, the need for collecting more human data has to be emphasized.

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