Hypoxia increases KIAA1199/CEMIP expression and enhances cell migration in pancreatic cancer

Pancreatic ductal adenocarcinoma (PDAC) is characterised by dense desmoplasia and hypoxic microenvironment. Our previous reports demonstrated that hyaluronan (HA), especially low-molecular-weight HA, provides a favourable microenvironment for PDAC progression. However, the effect of hypoxia on HA metabolism remains unknown. Using quantitative real-time RT-PCR and western blot analysis, we analysed the changes in the expression of HA-synthesizing enzymes (HAS2 and HAS3) and HA-degrading enzymes (HYAL1, KIAA1199/CEMIP) in PDAC cell lines under hypoxic conditions. Hypoxia increased the mRNA and protein expression of KIAA1199, whereas it decreased HYAL1 expression. The expression of HAS3 was increased and HAS2 remained unchanged in response to hypoxia. The effect of KIAA1199 on hypoxia-induced cell migration was determined using a transwell migration assay and small-interfering RNA (siRNA). Hypoxia enhanced the migratory ability of PDAC cells, which was inhibited by KIAA1199 knockdown. We also used immunohistochemistry to analyse the protein expression of hypoxia inducible factor (HIF) 1 alpha and KIAA1199 in PDAC tissues. There was a significant immunohistochemically positive correlation between KIAA1199 and HIF1 alpha. These findings suggest that hypoxia-induced KIAA1199 expression may contribute to enhanced motility in PDAC.

Automated summary

In pancreatic ductal adenocarcinoma (PDAC), hypoxia increases the expression of KIAA1199, decreases HYAL1 expression, and enhances HAS3 expression, thereby promoting the migratory ability of PDAC cells. This suggests that hypoxia-induced KIAA1199 expression may contribute to enhanced motility in PDAC.