HIF-1 alpha-induced miR-23a similar to 27a similar to 24 cluster promotes colorectal cancer progression via reprogramming metabolism

Tumor cells switch metabolic profile from oxidative phosphorylation to glycolysis in a hypoxic environment for survival and proliferation. The mechanisms governing this metabolic switch, however, remain incompletely understood. Here, we show that three miRNAs in the miR-23a similar to 27a similar to 24 cluster, miR-23a, miR-27a and miR-24, are the most upregulated miRNA cluster in colorectal cancer (CRC) under hypoxia. Gain- and loss-of-function assays, a human glucose metabolism array and gene pathway analyses confirm that HIF-1 alpha-induced miR23a similar to 27a similar to 24 cluster collectively regulate glucose metabolic network through regulating various metabolic pathways and targeting multiple tricarboxylic acid cycle (TCA)-related genes. In specific, miR-24/VHL/HIF-1 alpha in CRC form a double-negative feedback loop, which in turn, promotes the cellular transition to the 'high HIF-1 alpha/miR-24 and low VHL' state and facilitates cell survival. Our findings reveal that the miR-23a similar to 27a similar to 24 cluster is critical regulator switching CRC metabolism from oxidative phosphorylation to glycolysis, and controlling their expression can suppress colorectal cancer progression.