Iron is suspected to be involved in the induction and/or progression of var
ious human tumors. The present study was designed to investigate the effect
s of iron on endothelial cells, keeping in mind that the homeostasis of mic
rovessels plays a critical role in neo-angiogenesis. Applying a model of hu
man dermal microvascular endothelial cell terminal differentiation and deat
h induced by serum deprivation, we found that iron salts (iron chloride and
ferric nitrilotriacetate) provided a survival advantage to endothelial cel
ls. Using immunohistochemistry and Western blot analysis, we found that the
extended cellular life span induced by iron was paralleled by an increase
of Bcl-2 protein expression. Taken together, these observations suggest tha
t iron may give a survival advantage to endothelial cells and represent a n
ovel mechanism through which iron may contribute to tumorigenesis.