Should prolactin be reconsidered as a therapeutic target in human breast cancer?

Citation
V. Goffin et al., Should prolactin be reconsidered as a therapeutic target in human breast cancer?, MOL C ENDOC, 151(1-2), 1999, pp. 79-87
Citations number
71
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
MOLECULAR AND CELLULAR ENDOCRINOLOGY
ISSN journal
03037207 → ACNP
Volume
151
Issue
1-2
Year of publication
1999
Pages
79 - 87
Database
ISI
SICI code
0303-7207(19990525)151:1-2<79:SPBRAA>2.0.ZU;2-3
Abstract
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.