Expression of fibroblast growth factor-8 in adult rat tissues and human prostate carcinoma cells

被引:32
作者
Schmitt, JF
Hearn, MTW
Risbridger, GP
机构
[1] MONASH MED CTR,INST REPROD & DEV,CLAYTON,VIC 3168,AUSTRALIA
[2] MONASH UNIV,CTR BIOPROC TECHNOL,DEPT BIOCHEM & MOLEC BIOL,CLAYTON,VIC 3168,AUSTRALIA
关键词
D O I
10.1016/0960-0760(95)00259-6
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
Androgens are essential for normal prostatic and testicular function. However, paracrine and/or autocrine actions of a number of growth factors have been implicated in the function of these tissues. A recent addition to the fibroblast growth factor family, the so called androgen-induced growth factor (AIGF) or fibroblast growth factor-8 (FGF-8), has been proposed to be under strict androgen regulation and induction in the mouse mammary carcinoma cell line SC3. FGF-8, therefore, may have a local role in the prostate, which is known to be an androgen-responsive organ. This study reports, for the first time, the presence of FGF-8 mRNA in normal adult rat tissues (heart, brain, lung, kidney, testis, prostate and ovary), using an optimised reverse transcription and nested polymerase chain reaction (RT-PCR) procedure, although androgen-dependent FGF-8 expression was not demonstrated in these adult tissues. Consistent with the oncogenic characteristics of FGF-8, the corresponding mRNA was detected in the human prostate tumour cell lines LNCaP and DU145, Because the DU145 cell line is known to be androgen-independent, and the expression of FGF-8 mRNA in cultured LNCaP cells also occurred in the absence of exogenous androgens, it can be concluded that the expression of FGF-8 mRNA in these human cell lines, in the rat prostate and in other rat tissues is not under the regulation of androgens as hitherto proposed. Copyright (C) 1996 Elsevier Science Ltd
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页码:173 / 178
页数:6
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