Estrogen receptor mediated inhibition of cancer cell invasion and motility: An overview

被引:90
作者
Rochefort, H [1 ]
Platet, N [1 ]
Hayashido, Y [1 ]
Derocq, D [1 ]
Lucas, A [1 ]
Cunat, S [1 ]
Garcia, M [1 ]
机构
[1] Univ Montpellier 1, INSERM, Unite Hormones & Canc, U148, F-34090 Montpellier, France
关键词
D O I
10.1016/S0960-0760(98)00010-7
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
In this overview of results from our laboratory, we address the question of the role of estrogens during early steps of metastasis, involving cell invasion through the basement membrane and cell motility. The motility of several estrogen receptor (ER) positive breast (MCF7, T47D) and ovarian (BG-1, SKOV3, PEO4) cancer cell lines was studied using a modified Boyden chamber assay. We observed, in all cases, estradiol induced inhibition of cancer cell invasion and motility. A similar inhibitory effect of estradiol was found when the wild-type ER alpha was stably transfected in the ER-negative MDA-MB231 cells and 3Y1-Ad12 cancer cells. The mechanism of this inhibitory effect is unknown. In ovarian cancer, however, it may involve intermediary proteins such as fibulin-1, an extracellular matrix protein that strongly interacts with fibronectin and which is induced by estrogen and secreted by ovarian cancer cells. We conclude that estrogens in ER-positive breast and ovarian cancers have a dual effect, since they stimulate tumor growth but inhibit invasion and motility. This may be consistent with the good initial prognostic value of ER-positive breast cancers compared to ER negative breast cancers noted in several clinical studies. (C) 1998 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:163 / 168
页数:6
相关论文
共 41 条
[1]   17-BETA-ESTRADIOL REGULATES AND V-HA-RAS TRANSFECTION CONSTITUTIVELY ENHANCES MCF7 BREAST-CANCER CELL-INTERACTIONS WITH BASEMENT-MEMBRANE [J].
ALBINI, A ;
GRAF, J ;
KITTEN, GT ;
KLEINMAN, HK ;
MARTIN, GR ;
VEILLETTE, A ;
LIPPMAN, ME .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (21) :8182-8186
[2]  
ALBINI A, 1987, CANCER RES, V47, P3239
[3]   FIBULIN IS AN EXTRACELLULAR-MATRIX AND PLASMA GLYCOPROTEIN WITH REPEATED DOMAIN-STRUCTURE [J].
ARGRAVES, WS ;
TRAN, H ;
BURGESS, WH ;
DICKERSON, K .
JOURNAL OF CELL BIOLOGY, 1990, 111 (06) :3155-3164
[4]   MCF7 MAMMARY-CANCER CELLS RESPOND TO BFGF AND INTERNALIZE IT FOLLOWING ITS RELEASE FROM EXTRACELLULAR-MATRIX - A PERMISSIVE ROLE OF CATHEPSIN-D [J].
BRIOZZO, P ;
BADET, J ;
CAPONY, F ;
PIERI, I ;
MONTCOURRIER, P ;
BARRITAULT, D ;
ROCHEFORT, H .
EXPERIMENTAL CELL RESEARCH, 1991, 194 (02) :252-259
[5]   ESTROGENS STIMULATE CELL-PROLIFERATION AND INDUCE SECRETORY PROTEINS IN A HUMAN-BREAST CANCER CELL-LINE (T47D) [J].
CHALBOS, D ;
VIGNON, F ;
KEYDAR, I ;
ROCHEFORT, H .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1982, 55 (02) :276-283
[6]   Loss of heterozygosity at chromosome 6q in preinvasive and early invasive breast carcinomas [J].
Chappell, SA ;
Walsh, T ;
Walker, RA ;
Shaw, JA .
BRITISH JOURNAL OF CANCER, 1997, 75 (09) :1324-1329
[7]   Estrogens increase the expression of fibulin-1, an extracellular matrix protein secreted by human ovarian cancer cells [J].
Clinton, GM ;
Rougeot, C ;
Derancourt, J ;
Roger, P ;
Defrenne, A ;
Godyna, S ;
Argraves, WS ;
Rochefort, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (01) :316-320
[8]   ESTROGEN-INDUCED FACTORS OF BREAST-CANCER CELLS PARTIALLY REPLACE ESTROGEN TO PROMOTE TUMOR-GROWTH [J].
DICKSON, RB ;
MCMANAWAY, ME ;
LIPPMAN, ME .
SCIENCE, 1986, 232 (4757) :1540-1543
[9]   ESTRADIOL STIMULATES CELL-GROWTH AND SECRETION OF PROCATHEPSIN-D AND A 120-KILODALTON PROTEIN IN THE HUMAN OVARIAN-CANCER CELL-LINE BG-1 [J].
GALTIERDEREURE, F ;
CAPONY, F ;
MAUDELONDE, T ;
ROCHEFORT, H .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1992, 75 (06) :1497-1502
[10]  
GARCIA M, 1990, ONCOGENE, V5, P1809