Although prolactin (PRL) has been long suspected to be involved in the prog
ression of human breast cancer, the failure of clinical improvement by trea
tment with dopamine agonists, which lower circulating levels of PRL, rapidl
y reduced the interest of oncologists concerning a potential role of this p
ituitary hormone in the development of breast cancer. Within the last few y
ears, however, several studies reported first, that PRL is also synthesized
in the mammary gland, and second that it exerts its proliferative action i
n an autocrine/paracrine manner. These observations have led to a reconside
ration of the role of PRL as an active participant in breast cancer and are
an impetus to search for alternative strategies aimed at inhibiting the pr
oliferative effects of PRL on tumor mammary cells. In this report, we discu
ss the three possible levels that can be targeted for this purpose: the mam
mary synthesis of PRL, the interaction of the hormone with its receptor at
the surface of mammary cells, and the intracellular signaling cascades trig
gered by the activated receptor. For each of these steps, we discuss the mo
lecular event(s) that can be targeted, our understanding of the mechanisms
involving these putative targets as well as the tools currently available f
or their inhibition. Besides its proliferative effect, PRL is also involved
in the control of angiogenesis through one of its cleaved fragments, named
PRL 16K, which has been shown to inhibit the angiogenic process. In view o
f this biological activity, we discuss first the cleavage of PRL with respe
ct to the human mammary gland and, second, the hypothesis speculating that
a balance between the proliferative effect of intact PRL and the anti-angio
genic activity of its 16K-like fragments might be physiologically relevant
in the evolution of mammary tumors. If true, our hypothesis would suggest t
hat the enzymatic cleavage of PRL could represent a new molecular target in
the search for alternative strategies in the treatment of breast cancer. (
C) 1999 Elsevier Science Ireland Ltd. All rights reserved.