ALTERNATIVE MECHANISMS OF ACTION OF ANTIESTROGENS

被引:75
作者
COLLETTA, AA
BENSON, JR
BAUM, M
机构
[1] Section of Academic Surgery, Institute of Cancer Research, Royal Marsden Hospital, London, SW3 6JJ, Fulham Road
关键词
ANTIESTROGENS; CAMP PHOSPHODIESTERASE; GROWTH FACTORS; INSULIN-LIKE GROWTH FACTORS; PROTEIN KINASE C; TAMOXIFEN; TRANSFORMING GROWTH FACTOR BETA;
D O I
10.1007/BF00689672
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The molecular mechanism of action of anti-oestrogens such as tamoxifen appears to be a complex mixture of antagonism of the mitogenic action of oestradiol at the level of the oestrogen receptor, plus a range of other activities from enzyme inhibition to growth factor modulation. This article will concentrate on two specific areas: 1) the inhibition of protein kinase C and calmodulin-dependent cAMP phosphodiesterase; and 2) the regulation by tamoxifen of peptide regulators of breast cancer epithelial cell growth such as insulin-like growth factor I (IGF I) and transforming growth factor beta (TGF-beta). The elucidation of these mechanisms is potentially important in the treatment and chemoprevention of breast cancer-the quantitative contribution of each individual mechanism of the overall antineoplastic action of anti-oestrogens is central to developing new and possibly more effective anti-oestrogens and optimizing strategies for their use.
引用
收藏
页码:5 / 9
页数:5
相关论文
共 43 条
[31]   VARIATION OF THE INHIBITION OF CALMODULIN DEPENDENT CYCLIC-AMP PHOSPHODIESTERASE AMONGST ANALOGS OF TAMOXIFEN - CORRELATIONS WITH CYTOTOXICITY [J].
ROWLANDS, MG ;
PARR, IB ;
MCCAGUE, R ;
JARMAN, M ;
GODDARD, PM .
BIOCHEMICAL PHARMACOLOGY, 1990, 40 (02) :283-289
[32]  
SHOR SL, 1986, INT J CANCER, V37, P831
[33]   INSULIN-LIKE GROWTH-FACTORS STIMULATE CHEMOTAXIS IN HUMAN-MELANOMA CELLS [J].
STRACKE, ML ;
KOHN, EC ;
AZNAVOORIAN, SA ;
WILSON, LL ;
SALOMON, D ;
KRUTZSCH, HC ;
LIOTTA, LA ;
SCHIFFMANN, E .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 153 (03) :1076-1083
[34]  
SU HD, 1985, BIOCHEM PHARMACOL, V34, P3649
[35]   HIGH-AFFINITY ANTI-ESTROGEN BINDING-SITE DISTINCT FROM THE ESTROGEN-RECEPTOR [J].
SUTHERLAND, RL ;
MURPHY, LC ;
FOO, MS ;
GREEN, MD ;
WHYBOURNE, AM .
NATURE, 1980, 288 (5788) :273-275
[36]   DEFINITION OF 2 DISTINCT MECHANISMS OF ACTION OF ANTIESTROGENS ON HUMAN-BREAST CANCER CELL-PROLIFERATION USING HYDROXYTRIPHENYLETHYLENES WITH HIGH-AFFINITY FOR THE ESTROGEN-RECEPTOR [J].
SUTHERLAND, RL ;
WATTS, CKW ;
RUENITZ, PC .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1986, 140 (02) :523-529
[37]  
SUTHERLAND RL, 1983, CANCER RES, V43, P3998
[38]   TAMOXIFEN ATTENUATES PULSATILE GROWTH-HORMONE SECRETION - MEDIATION IN PART BY SOMATOSTATIN [J].
TANNENBAUM, GS ;
GURD, W ;
LAPOINTE, M ;
POLLAK, M .
ENDOCRINOLOGY, 1992, 130 (06) :3395-3401
[39]  
YEE D, 1988, CANCER RES, V48, P6691
[40]   ANALYSIS OF INSULIN-LIKE GROWTH FACTOR-I GENE-EXPRESSION IN MALIGNANCY - EVIDENCE FOR A PARACRINE ROLE IN HUMAN-BREAST CANCER [J].
YEE, D ;
PAIK, SY ;
LEBOVIC, GS ;
MARCUS, RR ;
FAVONI, RE ;
CULLEN, KJ ;
LIPPMAN, ME ;
ROSEN, N .
MOLECULAR ENDOCRINOLOGY, 1989, 3 (03) :509-517