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There has been an increasing number of studies contributing to the mechanistic understanding of aspirin’s anti-tumour effects in CRC including regulation of wingless-related integration site (Wnt), nuclear factor kappa light chain enhancer of activated B cells (NF-κB), hypoxia-inducible factor-1α (HIF-1α), mammalian target of rapamycin (mTOR), and phosphatidylinositol 3-kinase (PI3K) pathways which is the subject of excellent reviews ( Figure 1 ) [20, 22, 39, 40]
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