Prolactin acts as a potent survival factor for human breast cancer cell lines

被引:87
作者
Perks, CC [1 ]
Keith, AJ [1 ]
Goodhew, KL [1 ]
Savage, PB [1 ]
Winters, ZE [1 ]
Holly, JMP [1 ]
机构
[1] Bristol Royal Infirm & Gen Hosp, Dept CSSB, Div Surg, Bristol BS2 8HW, Avon, England
关键词
breast cancer; prolactin; apoptosis;
D O I
10.1038/sj.bjc.6601947
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Human breast cancer is the leading cause of cancer death in women from Western societies, and a large study of the epidemiology demonstrated strong associations between human prolactin and risk of breast cancer. Using established models of apoptosis of human breast cancer cell lines, we assessed the role of prolactin in breast cancer cell growth and survival. We showed that prolactin had no effect on the metabolic activity or total cell number of any cell lines. We confirmed endogenous prolactin production by these cells and that the levels varied. In the presence of a prolactin-neutralising antibody, each of the cell lines responded with the induction of apoptosis as opposed to growth inhibition. The sensitivity of the cell lines to the physiological inducer of apoptosis, C2-ceramide, appeared relative to the levels of endogenous prolactin that they contained. We then showed that exogenously added prolactin acted as a potent survival factor against apoptosis in all the cell lines examined. In addition, we demonstrated that a prolactin-neutralising antibody in combination with C2-ceramide caused an anticipated, additive increase in cell death. This study demonstrated that prolactin protects human breast cancer cell lines against apoptosis and this may have important implications for cancer treatment.
引用
收藏
页码:305 / 311
页数:7
相关论文
共 34 条
[1]   SERUM IMMUNOREACTIVE AND BIOACTIVE LACTOGENIC HORMONES IN ADVANCED BREAST-CANCER PATIENTS TREATED WITH BROMOCRIPTINE AND OCTREOTIDE [J].
ANDERSON, E ;
FERGUSON, JE ;
MORTEN, H ;
SHALET, SM ;
ROBINSON, EL ;
HOWELL, A .
EUROPEAN JOURNAL OF CANCER, 1993, 29A (02) :209-217
[2]  
Binart N, 2000, ADV EXP MED BIOL, V480, P85
[3]  
Bollengier F., 2001, Archives of Physiology and Biochemistry, V109, P180
[4]   TAMOXIFEN PLUS BROMOCRIPTINE VERSUS TAMOXIFEN PLUS PLACEBO IN ADVANCED BREAST-CANCER - RESULTS OF A DOUBLE-BLIND MULTICENTER CLINICAL-TRIAL [J].
BONNETERRE, J ;
MAURIAC, L ;
WEBER, B ;
ROCHE, H ;
FARGEOT, P ;
TUBIANAHULIN, M ;
SEVIN, M ;
CHOLLET, P ;
CAPPELAERE, P .
EUROPEAN JOURNAL OF CANCER & CLINICAL ONCOLOGY, 1988, 24 (12) :1851-1853
[5]  
Chen WY, 1999, CLIN CANCER RES, V5, P3583
[6]  
CLEVENGER CV, 1995, AM J PATHOL, V146, P695
[7]   The role of prolactin in mammary carcinoma [J].
Clevenger, CV ;
Furth, PA ;
Hankinson, SE ;
Schuler, LA .
ENDOCRINE REVIEWS, 2003, 24 (01) :1-27
[8]   Protective effect of prolactin and placental lactogen on NO-induced Nb2 lymphoma cell apoptosis [J].
Fernández, ML ;
Iglesias, MM ;
Biron, VA ;
Wolfenstein-Todel, C .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2003, 416 (02) :249-256
[9]  
FIELDS K, 1993, LAB INVEST, V68, P354
[10]   PROLACTIN RECEPTOR ANTAGONISTS THAT INHIBIT THE GROWTH OF BREAST-CANCER CELL-LINES [J].
FUH, G ;
WELLS, JA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (22) :13133-13137