Abstract

Type 2 diabetes mellitus (T2DM) is associated with a higher risk of cancer and cancer-related mortality. Increased blood glucose and insulin levels in T2DM patients may be, at least in part, responsible for this effect. Indeed, lowering glucose and/or insulin levels pharmacologically appears to reduce cancer risk and progression, as has been demonstrated for the biguanide metformin in observational studies. Studies investigating the influence of sulfonylurea derivatives (SUs) on cancer risk have provided conflicting results, partly due to comparisons with metformin. Furthermore, little attention has been paid to within-class differences in systemic and off-target effects of the SUs. The aim of this systematic review is to discuss the available preclinical and clinical evidence on how the different SUs influence cancer development and risk. Databases including PubMed, Cochrane, Database of Abstracts on Reviews and Effectiveness, and trial registries were systematically searched for available clinical and preclinical evidence on within-class differences of SUs and cancer risk. The overall preclinical and clinical evidence suggest that the influence of SUs on cancer risk in T2DM patients differs between the various SUs. Potential mechanisms include differing affinities for the sulfonylurea receptors and thus differential systemic insulin exposure and off-target anti-cancer effects mediated for example through potassium transporters and drug export pumps. Preclinical evidence supports potential anti-cancer effects of SUs, which are of interest for further studies and potentially repurposing of SUs. At this time, the evidence on differences in cancer risk between SUs is not strong enough to guide clinical decision making.

Highlights

  • Patients diagnosed with type 2 diabetes mellitus (T2DM) have an increased risk of cancer and cancer-related mortality (Chen et al, 2017b; Giovannucci et al, 2010)

  • Data on cancer risk was found for gliclazide, glimepiride, glibenclamide and tolbutamide use; no data was found for the other sulfonylurea derivatives (SUs) of interest

  • One study showed that the reduced cancer risk in gliclazide users was dose-dependent (Yang et al, 2010a)

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Summary

Introduction

Patients diagnosed with type 2 diabetes mellitus (T2DM) have an increased risk of cancer and cancer-related mortality (Chen et al, 2017b; Giovannucci et al, 2010). Cancer cells have an altered energy metabolism characterized by high glucose consumption and high glycolysis rates This provides energy to generate ATP as well as metabolic intermediates for production of biomass required for cellular proliferation (Liberti and Locasale, 2016). The various classes of glucoselowering agents have different mechanisms of action, and differential effects on plasma glucose and insulin levels and different offtarget effects These classes of drugs may differ in their influence on cancer risk and development. The aim of this systematic review is to discuss the available preclinical and clinical evidence on differences in cancer risk and development between patients treated with different SU drugs Understanding these so-called within-SU class differences is important to understand the conflicting data regarding cancer risk of SUs and to determine whether sufficient data is available to guide clinical selection of SUs for glycemic control. The accumulated preclinical and clinical evidence of the differential effects of SUs on cancer risk in T2DM patients may help to identify novel cancer treatment targets

Search strategy
Differences between SUs in blood glucose lowering capacity
Differences between SUs in cancer risk: clinical evidence
Gliclazide
Glibenclamide
Design
Glimepiride
Tolbutamide
Conclusions clinical evidence
Effect of SUs on cancer cell growth
Effects of SUs on growth factors and growth factor pathways
Effects of SUs on ATP-binding cassette transporters and solute channels
Effects of SUs on angiogenesis and metastasis
The effects of SUs on anti-cancer treatment
Discussion
Full Text
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