• miR-373-3p promotes aerobic glycolysis and proliferation in colon cancer cells by directly targeting and inhibiting MFN2 expression.
• In vivo, miR-373-3p enhances tumor growth and lactate production in a nude mouse model, while miR-373-3p antagomir suppresses tumor growth.
• In human colon cancer tissues, miR-373-3p is upregulated and MFN2 mRNA is downregulated, with an inverse correlation.
• Targeting miR-373-3p represents a potential therapeutic strategy for colon cancer treatment.
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