Effect of leuprorelin acetate on cell growth and prostate-specific antigen gene expression in human prostatic cancer cells

被引:25
作者
Sica, G
Iacopino, F
Settesoldi, D
Zelano, G
机构
[1] Univ Cattolica Sacro Cuore, Fac Med & Chirurg, Ist Istol & Embriol, I-00168 Rome, Italy
[2] Univ Cattolica Sacro Cuore, Fac Med & Chirurg, Ist Anat Umana Normale, I-00168 Rome, Italy
关键词
leuprorelin; prostatic cancer cells; proliferation; prostate-specific antigen;
D O I
10.1159/000052300
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Objectives: We investigated modulation of cell growth and prostate-specific antigen (PSA) gene expression in prostatic cancer cells by the luteinizing hormone-releasing hormone analog (LH-RHa), leuprorelin acetate, alone or combined with other agents. Methods: The effect of the analog on proliferation of both androgen-sensitive and -insensitive prostate cancer cells, maintained in different culture conditions, was evaluated by cell counts at various intervals of time. Basal expression of PSA gene and its variations were determined by a reverse transcriptase-polymerase chain reaction assay. Results: LH-RHa is ineffective in regulating cell growth, when used alone in both hormone-sensitive and -insensitive cell lines. Nevertheless, it counteracts the stimulatory action of androgens on proliferation of LNCaP cells, which respond to low concentrations of dihydrotestosterone. Moreover, LH-RHa has an inhibitory effect on the mitogenic action of epidermal growth factor (EGF) in androgen-unresponsive PC-3 cells. The analog reduces PSA gene expression in both hormone-sensitive and -insensitive cells. Interestingly, it counteracts the gene expression induced by androgens in LNCaP cells and by EGF in PC-3 cells. Conclusions: These data show that LH-RHa may behave like a negative growth factor, which directly regulates cell growth and PSA gene expression. Moreover, our findings support the idea that growth factors may interfere with the androgen signalling pathway.
引用
收藏
页码:2 / 8
页数:7
相关论文
共 16 条
[1]   TRANSCRIPTION OF THE DYSTROPHIN GENE IN HUMAN-MUSCLE AND NON-MUSCLE TISSUES [J].
CHELLY, J ;
KAPLAN, JC ;
MAIRE, P ;
GAUTRON, S ;
KAHN, A .
NATURE, 1988, 333 (6176) :858-860
[2]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P15
[3]  
CULIG Z, 1994, CANCER RES, V54, P5474
[4]  
DONDI D, 1994, CANCER RES, V54, P4091
[5]   LNCaP prostatic adenocarcinoma cells derived from low and high passage numbers display divergent responses not only to androgens but also to retinoids [J].
Esquenet, M ;
Swinnen, JV ;
Heyns, W ;
Verhoeven, G .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1997, 62 (5-6) :391-399
[6]  
FOEKENS JA, 1987, HORMONAL MANIPULATIO, P369
[7]   A COMPARATIVE-STUDY ON EXPRESSION OF PROSTATIC INHIBIN PEPTIDE, PROSTATE ACID-PHOSPHATASE AND PROSTATE-SPECIFIC ANTIGEN IN ANDROGEN-INDEPENDENT HUMAN AND RAT PROSTATE CARCINOMA CELL-LINES [J].
GARDE, SV ;
SHETH, AR ;
PORTER, AT ;
PIENTA, KJ .
CANCER LETTERS, 1993, 70 (03) :159-166
[8]   MOLECULAR STAGING OF PROSTATE-CANCER WITH THE USE OF AN ENHANCED REVERSE-TRANSCRIPTASE PCR ASSAY [J].
KATZ, AE ;
OLSSON, CA ;
RAFFO, AJ ;
CAMA, C ;
PERLMAN, H ;
SEAMAN, E ;
OTOOLE, KM ;
MCMAHON, D ;
BENSON, MC ;
BUTTYAN, R .
UROLOGY, 1994, 43 (06) :765-775
[9]  
LIMONTA P, 1992, J CLIN ENDOCR METAB, V75, P207, DOI 10.1210/jc.75.1.207
[10]   GROWTH-INHIBITION OF HUMAN PROSTATE TUMOR-CELLS BY AN AGONIST OF GONADOTROPIN-RELEASING-HORMONE [J].
LOOP, SM ;
GORDER, CA ;
LEWIS, SM ;
SAIERS, JH ;
DRIVDAHL, RH ;
OSTENSON, RC .
PROSTATE, 1995, 26 (04) :179-188