Differential regulation of normal and tumoral breast epithelial cell growth by fibroblasts and 1,25-dihydroxyvitamin D3

被引:10
作者
Gache, C
Berthois, Y
Cvitkovic, E
Martin, PM
Saez, S
机构
[1] Fac Med Secteur Nord Marseille, IFR Jean Roche, CJF INSERM 9311, Lab Interact Cellulaires Intratumorales, F-13916 Marseille 20, France
[2] Ctr Hosp Lyon Sud, Serv Chirurg Oncol, F-69310 Pierre Benite, France
[3] Hop Paul Brousse, Serv Oncol Malad Sanguines Immunitaires & Tumoral, Villejuif, France
关键词
breast cancer; cell interactions; 1,25-dihydroxyvitamin D-3; fibroblast; normal epithelial cell;
D O I
10.1023/A:1006163418479
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mesenchymal-epithelial interactions are of paramount importance during normal and tumoral breast developments. We have investigated the paracrine growth regulation of normal and tumoral breast epithelial cells by fibroblasts derived from normal or pathological breast tissues. In some cases, breast cancer MCF-7 cells or normal epithelial cells in primary culture were cocultured with fibroblasts in a Transwell system allowing diffusible factor exchanges. Alternatively, conditioned medium produced by fibroblast cultures was added to epithelial cell cultures. Fibroblasts were shown to stimulate the proliferation of normal and carcinoma cells through paracrine mechanisms. However, the paracrine exchanges appeared to be different in normal versus tumoral breast epithelial cell growth regulation. Moreover, vitamin D-related compounds that have been proposed as anti-tumoral drugs were studied for their ability to affect normal and tumoral mammary epithelial cell proliferation and to interfere with the growth-regulatory activity of fibroblasts. Whereas vitamin D compounds inhibited MCF-7 cell growth, they led to a marked stimulation of the proliferation of normal mammary epithelial cells. Moreover, it was shown that the vitamin D analog EB 1089 can block the mitogenic effect of fibroblast-conditioned medium on tumoral but not normal breast epithelial cells. The differential effects of vitamin D compounds on cell proliferation provide further data in favor of the different behaviours of normal and tumoral mammary epithelial cells. The potential therapeutic use of vitamin D derivatives in the treatment of breast cancer is supported by these results but their growth-stimulatory properties on normal epithelial cells cannot be overlooked.
引用
收藏
页码:29 / 39
页数:11
相关论文
共 47 条
[1]   SELECTIVE INTERACTIONS BETWEEN MAMMARY EPITHELIAL-CELLS AND FIBROBLASTS IN COCULTURE [J].
ADAM, L ;
CREPIN, M ;
LELONG, JC ;
SPANAKIS, E ;
ISRAEL, L .
INTERNATIONAL JOURNAL OF CANCER, 1994, 59 (02) :262-268
[2]   EFFECTS OF HUMAN-BREAST FIBROBLASTS ON GROWTH AND 17-BETA-ESTRADIOL DEHYDROGENASE-ACTIVITY OF MCF-7 CELLS IN CULTURE [J].
ADAMS, EF ;
NEWTON, CJ ;
BRAUNSBERG, H ;
SHAIKH, N ;
GHILCHIK, M ;
JAMES, VHT .
BREAST CANCER RESEARCH AND TREATMENT, 1988, 11 (02) :165-172
[3]  
Bourhis XFDL, 1997, INT J CANCER, V71, P42, DOI 10.1002/(SICI)1097-0215(19970328)71:1<42::AID-IJC9>3.3.CO
[4]  
2-X
[5]   FIBROBLAST-MEDIATED DIFFERENTIATION IN HUMAN BREAST-CARCINOMA CELLS (MCF-7) GROWN AS NODULES IN-VITRO [J].
BROUTYBOYE, D ;
MAINGUENE, C ;
MAGNIEN, V ;
ISRAEL, L ;
BEAUPAIN, R .
INTERNATIONAL JOURNAL OF CANCER, 1994, 56 (05) :731-735
[6]   VITAMIN-D RECEPTORS IN BREAST-CANCER CELLS [J].
BURAS, RR ;
SCHUMAKER, LM ;
DAVOODI, F ;
BRENNER, RV ;
SHABAHANG, M ;
NAUTA, RJ ;
EVANS, SRT .
BREAST CANCER RESEARCH AND TREATMENT, 1994, 31 (2-3) :191-202
[7]   1,25-DIHYDROXYVITAMIN-D3 INHIBITORY EFFECT ON THE GROWTH OF 2 HUMAN-BREAST CANCER CELL-LINES (MCF-7, BT-20) [J].
CHOUVET, C ;
VICARD, E ;
DEVONEC, M ;
SAEZ, S .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1986, 24 (01) :373-376
[8]   HORMONAL ASPECTS OF BREAST-CANCER - GROWTH-FACTORS, DRUGS AND STROMAL INTERACTIONS [J].
CLARKE, R ;
DICKSON, RB ;
LIPPMAN, ME .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 1992, 12 (01) :1-23
[9]   EB1089 - A NEW VITAMIN-D ANALOG THAT INHIBITS THE GROWTH OF BREAST-CANCER CELLS INVIVO AND INVITRO [J].
COLSTON, KW ;
MACKAY, AG ;
JAMES, SY ;
BINDERUP, L ;
CHANDER, S ;
COOMBES, RC .
BIOCHEMICAL PHARMACOLOGY, 1992, 44 (12) :2273-2280
[10]  
CUNHA GR, 1994, CANCER, V74, P1030, DOI 10.1002/1097-0142(19940801)74:3+<1030::AID-CNCR2820741510>3.0.CO