The role of prolactin and growth hormone in breast cancer

被引:94
作者
Wennbo, H
Törnell, J [1 ]
机构
[1] Univ Gothenburg, Dept Physiol, Gothenburg, Sweden
[2] Astra Transgen Ctr, Molndal, Sweden
关键词
prolactin; growth hormone; transgenic mice; mammary cancer; auto/paracrine;
D O I
10.1038/sj.onc.1203349
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This review will focus on the role for prolactin (PRL) and growth hormone (GH) in mammary tumor formation. Much attention has previously been focused on circulating levels of GH/PRL in relation to mammary tumor formation. We will review data demonstrating that these ligands also could be produced locally in different organs, including the mammary gland and mammary tumors, and suggest that this local production may be of importance for pathological conditions. We will also discuss mechanisms for crosstalk between steroids and GH/PRL. A crosstalk between GH- and PRL response is possible at multiple levels. In the human, GH can activate both the prolactin receptor (PRLR) and the growth hormone receptor (GHR), We have demonstrated that activation of the PRLR, but not the GHR, is inducing mammary tumors in transgenic mice. Furthermore, the elevated levels of insulin-like growth factor 1 (IGF-I) seen in the GHR activating transgenic mice is not sufficient for tumor induction. The induced tumors express functionally active prolactin that could be of importance for the tumor formation. Paracrine/aurocrine stimulation by PRL may be more important than PRL transported via the circulation. In women, the role for stimulation of the PRLR and/or the GHR in mammary tumor formation has not been proven, although experiments from primates suggest that the PRLR could be of importance.
引用
收藏
页码:1072 / 1076
页数:5
相关论文
共 56 条
[1]   THE ANTERIOR PITUITARY-GRAFTED RAT - A VALID MODEL OF CHRONIC HYPERPROLACTINEMIA [J].
ADLER, RA .
ENDOCRINE REVIEWS, 1986, 7 (03) :302-313
[2]   Extrapituitary prolactin: Distribution, regulation, functions, and clinical aspects [J].
BenJonathan, N ;
Mershon, JL ;
Allen, DL ;
Steinmetz, RW .
ENDOCRINE REVIEWS, 1996, 17 (06) :639-669
[3]  
BONNETERRE J, 1987, CANCER RES, V47, P4724
[4]   CLONING AND EXPRESSION OF THE RAT PROLACTIN RECEPTOR, A MEMBER OF THE GROWTH-HORMONE PROLACTIN RECEPTOR GENE FAMILY [J].
BOUTIN, JM ;
JOLICOEUR, C ;
OKAMURA, H ;
GAGNON, J ;
EDERY, M ;
SHIROTA, M ;
BANVILLE, D ;
DUSANTERFOURT, I ;
DJIANE, J ;
KELLY, PA .
CELL, 1988, 53 (01) :69-77
[5]   MICROADENOMAS OF THE PITUITARY AND ABNORMAL SELLAR TOMOGRAMS IN AN UNSELECTED AUTOPSY SERIES [J].
BURROW, GN ;
WORTZMAN, G ;
REWCASTLE, NB ;
HOLGATE, RC ;
KOVACS, K .
NEW ENGLAND JOURNAL OF MEDICINE, 1981, 304 (03) :156-158
[6]  
CLEVENGER CV, 1995, AM J PATHOL, V146, P695
[7]   Prolactin recruits STAT1, STAT3 and STAT5 independent of conserved receptor tyrosines TYR402, TYR479, TYR515 and TYR580 [J].
DaSilva, L ;
Rui, H ;
Erwin, RA ;
Howard, OMZ ;
Kirken, RA ;
Malabarba, MG ;
Hackett, RH ;
Larner, AC ;
Farrar, WL .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1996, 117 (02) :131-140
[8]  
DECOUVELAERE C, 1995, CELL GROWTH DIFFER, V6, P477
[9]   ELEVATED GROWTH-HORMONE LEVELS IN SERA FROM BREAST-CANCER PATIENTS [J].
EMERMAN, JT ;
LEAHY, M ;
GOUT, PW ;
BRUCHOVSKY, N .
HORMONE AND METABOLIC RESEARCH, 1985, 17 (08) :421-424
[10]   EVIDENCE THAT THE GROWTH-HORMONE RECEPTOR MEDIATES DIFFERENTIATION AND DEVELOPMENT OF THE MAMMARY-GLAND [J].
FELDMAN, M ;
RUAN, WF ;
CUNNINGHAM, BC ;
WELLS, JA ;
KLEINBERG, DL .
ENDOCRINOLOGY, 1993, 133 (04) :1602-1608