Besides the anti-thrombotic features, it demonstrated anti-cancer activities in multiple in vitro studies, inhibiting various molecules and pathways such as receptor tyrosine kinases, PI3K-AKT pathway, and immune checkpoints PD-L1 and CD47, decreasing cell proliferation and inducing apoptosis in different cancers, including NSCLC and AML [128,129]. The gene discussed is AKT1; the disease is acute myeloid leukemia.