Key result
Peruvoside suppresses leukemia cell growth more potently than ouabain and digitoxin at nanomolar concentrations.
Why the study?
Leukemia remains difficult to cure due to frequent relapses driven by leukemic stem cells, and cardiac glycosides have potential as anti-leukemia agents but require further evaluation.
Answers are grounded in this paper and cite their sources.
Peruvoside merits further preclinical leukemia studies; hypothesis-generating and should not yet change practice.
Despite the available chemotherapy and treatment, leukemia remains a difficult disease to cure due to frequent relapses after treatment. Among the heterogeneous leukemic cells, a rare population referred as the leukemic stem cell (LSC), is thought to be responsible for relapses and drug resistance. Cardiac glycosides (CGs) have been used in treating heart failure despite its toxicity. Recently, increasing evidence has demonstrated its new usage as a potential anti-cancer drug. Ouabain, one of the CGs, specifically targeted CD34⁺CD38(-) leukemic stem-like cells, but not the more mature CD34⁺CD38⁺ leukemic cells, making this type of compounds a potential treatment for leukemia. In search of other potential anti-leukemia CGs, we found that Peruvoside, a less studied CG, is more effective than Ouabain and Digitoxin at inducing cell death in primitive myeloid leukemia cells without obvious cytotoxicity on normal blood cells. Similar to Ouabain and Digitoxin, Peruvoside also caused cell cycle arrest at G₂/M stage. It up-regulates CDKN1A expression and activated the cleavage of Caspase 3, 8 and PARP, resulting in apoptosis. Thus, Peruvoside showed potent anti-leukemia effect, which may serve as a new anti-leukemia agent in the future.
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Leong et al. (2016) studied Acute myeloid leukemia (AML) and chronic myelogenous leukemia (CML). Peruvoside vs. DMSO, Ouabain, Digitoxin was evaluated on Cell viability (IC50) at 24 hours. Peruvoside effectively induced apoptosis and inhibited cell growth in human primitive AML KG1a cells (IC50 26 nM) and CML K562 cells (IC50 75 nM) more potently than Ouabain and Digitoxin.
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