Hyperglycaemia and aberrated insulin signalling stimulate tumour progression via induction of the extracellular matrix component hyaluronan |
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| Authors: | Sören Twarock Christina Reichert Ulrike Peters Daniel J. Gorski Katharina Röck Jens W. Fischer |
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| Affiliation: | Institut für Pharmakologie und Klinische Pharmakologie, Universit?tsklinikum der Heinrich‐Heine‐Universit?t, Düsseldorf, Germany |
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| Abstract: | Epidemiological studies have detected a higher incidence of various tumour entities in diabetic patients. However, the underlying mechanisms remain insufficiently understood. Glucose‐derived pericellular and extracellular hyaluronan (HA) promotes tumour progression and development. In our study, we tested the hypothesis that a diabetic metabolic state, characterised by hyperglycaemia and concomitant aberrant insulin signalling, stimulates tumour progression via the induction of HA synthesis. In a streptozotocin‐induced diabetic nude mouse tumour xenograft model, hyperglycaemia and lack of insulin caused an increased formation of tumour‐associated HA‐matrix, which in turn accelerated tumour progression and neoangiogenesis. This process was effectively attenuated by treatment with 4‐methylumbelliferone, a pharmacological inhibitor of HA‐synthesis. To define the mechanisms behind these in vivo observations, we investigated the impact of hyperglycaemia and insulin on the glucose metabolism in oesophageal squamous cell cancer cells (ESCC). Hyperglycaemia induced HA synthesis while insulin diminished HA production by directing glucose metabolites to glycolysis. Vice versa, inhibition of glycolysis, either by knockdown of the glycolytic key enzyme phosphofructokinase or by an experimental abrogation of insulin signalling (knockdown of the insulin receptor and long‐term treatment with insulin) augmented HA synthesis. Consequently, these processes induced invasion, anchorage‐independent growth and adhesion of ESCC to endothelial cells in vitro. Thus, the cellular shift in glucose usage from catabolism of glucose to anabolism of HA driven by hyperglycaemia and insulin resistance may represent an important link between diabetes and cancer progression. Hence, therapeutical inhibition of HA synthesis may represent a promising approach for tumour treatment in diabetic patients. |
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| Keywords: | diabetes oesophageal cancer extracellular matrix hyaluronan 4‐methyumbelliferone pharmacological therapy |
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