Retinoid-dependent growth inhibition, differentiation and apoptosis in acute promyelocytic leukemia cells. Expression and activation of caspases

In the NB4 model of acute promyelocytic leukemia (APL), ATRA, g-cis retinoi c acid (g-cis RA), the pan-RAR and RAR alpha-selective agonists, TTNPB and AM580, induce growth inhibition, granulocytic differentiation and apoptosis , By contrast, two RXR agonists, a RAR beta agonist and an anti-AP1 retinoi d have very limited activity, ATRA- and AM580-dependent effects are complet ely inhibited by RAR antagonistic blockade, while 9-cis RA-induced cell-gro wth-inhibition and apoptosis are equally inhibited by RAR and RXR antagonis ts, ATRA, g-cis RA and AM580 cause upregulation of the mRNAs coding for pro -caspase-1, -7, -8, and -9, which, however, results in increased synthesis of only pro-caspase-1 and -7 proteins, These phenomena are associated with activation of pro-caspase-6, -7 and -8, cytochrome c release from the mitoc hondria, inversion of Bcl-2/Bax ratio and degradation of PML-RAR alpha. Cas pase activation is fundamental for retinoid-induced apoptosis, which is sup pressed by the caspase-inhibitor z-VAD.