Galectin-1 has been demonstrated to be a mediator of T-cell apoptosis actin
g on activated T-cells and, in a selective manner, on different T leukemia
cell lines. Here we show that the sensitivity to galectin-1 is associated w
ith repression of the endogenous galectin-1 gene whereas nonsensitive cells
express high levels of galectin-1. Repression of galectin-1 gene in sensit
ive cells is associated with hypermethylation of the promoter region. Trans
ient treatment of nonexpressing cells with the demethylating agent 5-azacyt
idine led to irreversible demethylation and subsequent reactivation of gale
ctin-1 gene.