Apoptotic and Cell Cycle Effects of Triterpenes Isolated from Phoradendron wattii on Leukemia Cell Lines.
Lía S Valencia-ChanDafne Moreno-LorenzanaJimmy Josué Ceballos-CruzSergio R Peraza-SánchezAntonieta Chávez-GonzálezMoo-Puc Rosa EstherPublished in: Molecules (Basel, Switzerland) (2022)
Current antineoplastic agents present multiple disadvantages, driving an ongoing search for new and better compounds. Four lupane-type triterpenes, 3α,24-dihydroxylup-20(29)-en-28-oic acid ( 1 ), 3α,23-dihydroxy-30-oxo-lup-20(29)-en-28-oic acid ( 2 ), 3α,23- O -isopropylidenyl-3α,23-dihydroxylup-20(29)-en-28-oic acid ( 3 ), and 3α,23-dihydroxylup-20(29)-en-28-oic acid ( 4 ), previously isolated from Phoradendron wattii , were evaluated on two cell lines of chronic (K562) and acute (HL60) myeloid leukemia. Compounds 1 , 2 , and 4 decreased cell viability and inhibit proliferation, mainly in K562, and exhibited an apoptotic effect from 24 h of treatment. Of particular interest is compound 2 , which caused arrest in active phases (G2/M) of the cell cycle, as shown by in silico study of the CDK1/Cyclin B/Csk2 complex by molecular docking. This compound [3α,23-dihydroxy-30-oxo-lup-20(29)-en-28-oic acid] s a promising candidate for incorporation into cancer treatments and deserves further study.