Abstract
Background and Objective: All-trans retinoic acid (ATRA) is only effective in acute promyelocytic leukemia (APL), but not in other subtype of acute myeloid leukemia (AML). Salinomycin targets tumor cells rather than non-tumorigenic cells, and WNT/β-catenin pathway inhibition is one of the mechanisms of its anti-tumor activity. There is a crosstalk between RA and WNT/β-catenin pathway. Here, we investigate the effect of the combination of salinomycin and ATRA (S+RA) in non-APL AML cells.
Methods: Apoptosis was evaluated by cell viability and Annexin-V assay. Cell differentiation was analyzed by CD11c expression and morphology. To explore the underlying mechanisms, Western blot analysis and mitochondrial transmembrane potentials (ΔΨm) were used.
Results & Discussion: S+RA induced differentiation and apoptosis in AML cell lines and AML primary cells. S+RA inhibited the β-catenin signal pathway as determined by the decreased protein levels of β-catenin, the low-density lipoprotein receptor-related proteins 6 (LRP6), and its downstream proteins such as survivin, c-Myc, caspase-3/7, cdc25A and cyclinD1 and reduced phosphorylation level of GSK3β S9. S+RA also increased the protein levels of CCAAT/enhancer-binding proteins (C/EBPs) and PU.1 and collapsed Δψm. The above molecular and cellular changes induced by S+RA were inhibited by β-catenin specific activator and promoted by β-catenin specific inhibitor.
Conclusion: S+RA induced differentiation by β-catenin-inhibition-mediated up-regulation of C/EBPs and PU.1 and suppression of c-Myc. S+RA triggered apoptosis through β-catenin-inhibition-regulated ΔΨm collapse and caspase-3/7 activation. Taken together, our findings may provide novel therapeutic strategies for AML patients by targeting the WNT/β-catenin pathway.
Graphical Abstract
[http://dx.doi.org/10.1038/s41408-021-00425-3] [PMID: 33619261]
[http://dx.doi.org/10.1182/blood.V72.2.567.567] [PMID: 3165295]
[PMID: 29980141]
[http://dx.doi.org/10.1038/nature01593] [PMID: 12717450]
[http://dx.doi.org/10.1038/nri1529] [PMID: 15630426]
[http://dx.doi.org/10.1038/sj.leu.2404239] [PMID: 16688229]
[http://dx.doi.org/10.1038/sj.leu.2404732] [PMID: 17554387]
[http://dx.doi.org/10.1126/science.1186624] [PMID: 20339075]
[http://dx.doi.org/10.1038/nature12883] [PMID: 24429522]
[http://dx.doi.org/10.1007/s00432-020-03407-3] [PMID: 32980885]
[http://dx.doi.org/10.1158/1078-0432.CCR-17-1556] [PMID: 29463558]
[http://dx.doi.org/10.1007/s12185-016-2116-x] [PMID: 27766528]
[http://dx.doi.org/10.3390/cancers12092696] [PMID: 32967262]
[http://dx.doi.org/10.1016/S0960-9822(00)80088-3] [PMID: 10607566]
[http://dx.doi.org/10.1371/journal.pone.0143255] [PMID: 26571119]
[http://dx.doi.org/10.1089/scd.2019.0065] [PMID: 31337269]
[http://dx.doi.org/10.1177/1010428317695035] [PMID: 28349817]
[http://dx.doi.org/10.3892/or.2018.6513] [PMID: 29989650]
[http://dx.doi.org/10.18632/oncotarget.11866] [PMID: 27612428]
[http://dx.doi.org/10.1016/j.bbrc.2010.03.138] [PMID: 20350531]
[http://dx.doi.org/10.1073/pnas.1110431108] [PMID: 21788521]
[http://dx.doi.org/10.1182/blood.V83.11.3298.3298] [PMID: 8193365]
[http://dx.doi.org/10.1080/10428194.2021.1961231] [PMID: 34355652]
[PMID: 31218101]
[http://dx.doi.org/10.1038/18884] [PMID: 10201372]
[http://dx.doi.org/10.1016/j.ccr.2011.03.010] [PMID: 21575861]
[http://dx.doi.org/10.1038/sj.onc.1208433] [PMID: 15782138]
[http://dx.doi.org/10.3390/cells9010023] [PMID: 31861751]
[http://dx.doi.org/10.1016/S0092-8674(02)01014-0] [PMID: 12408868]
[http://dx.doi.org/10.1002/ijc.30662] [PMID: 28224619]
[PMID: 33437364]
[http://dx.doi.org/10.1038/leu.2016.146] [PMID: 27211263]
[http://dx.doi.org/10.1042/bj20030426] [PMID: 12954078]
[http://dx.doi.org/10.1038/ng1679] [PMID: 16311598]
[http://dx.doi.org/10.1016/j.exphem.2008.01.015] [PMID: 18375040]
[http://dx.doi.org/10.1172/JCI2887] [PMID: 10330422]
[http://dx.doi.org/10.1128/MCB.02422-06] [PMID: 17562868]
[http://dx.doi.org/10.1038/sj.onc.1205400] [PMID: 12032779]
[http://dx.doi.org/10.1002/cphy.c190014] [PMID: 31853969]