MacDonald A, Habib F K
University Department of Surgery, Western General Hospital, Edinburgh, UK.
Br J Cancer. 1992 Feb;65(2):177-82. doi: 10.1038/bjc.1992.37.
The present study was undertaken to compare the relationship between response to exogenous epidermal growth factor (EGF) and the expression of the EGF-receptor (EGF-R) in an androgen sensitive (LNCaP) and insensitive (DU145) prostate cancer cell line. Although both cell lines demonstrated a single EGF-R binding site of similar high affinities (mean dissociation constant (Kd) +/- S.D. for DU145 = 1.0 +/- 0.6 nmol l-1; LNCaP = 2.8 +/- 2.2 nmol l-1) the number of binding sites (RT) for the hormone insensitive DU145 cells (mean +/- S.D. = 2.5 +/- 1.0 x 10(5) sites/cell) and 10-fold greater than that expressed in the androgen responsive LNCaP cell line (mean +/- S.D. = 2.0 +/- 1 x 10(4) sites/cell). Additionally exogenous EGF only minimally affected the growth and DNA synthesis of DU145 cells whereas LNCaP cells showed a significant response which was dose dependent. The autologous production of EGF-like molecules by DU145 cells is believed to reduce the cells needs for exogenous mitogens, thereby rendering the cells autostimulatory. Treatment of LNCaP cells with Mibolerone--a synthetic androgen--did not affect either the expression of the EGF receptor or the proliferative response observed with EGF. Western blot analysis, using monoclonal antibodies directed against the EGF receptor revealed a band of approximately 170 kD with DU145 cell lysates but the LNCaP EGF receptor was not detected using this technique.
本研究旨在比较雄激素敏感(LNCaP)和不敏感(DU145)前列腺癌细胞系对外源性表皮生长因子(EGF)的反应与EGF受体(EGF-R)表达之间的关系。虽然两种细胞系都显示出具有相似高亲和力的单一EGF-R结合位点(DU145的平均解离常数(Kd)±标准差 = 1.0±0.6 nmol l-1;LNCaP = 2.8±2.2 nmol l-1),但激素不敏感的DU145细胞的结合位点数量(RT)(平均±标准差 = 2.5±1.0×10(5) 个位点/细胞)比雄激素反应性LNCaP细胞系中表达的结合位点数量高10倍(平均±标准差 = 2.0±1×10(4) 个位点/细胞)。此外,外源性EGF仅对DU145细胞的生长和DNA合成有最小程度的影响,而LNCaP细胞则表现出显著的剂量依赖性反应。据信DU145细胞自身产生的EGF样分子可减少细胞对外源性有丝分裂原的需求,从而使细胞具有自刺激作用。用合成雄激素米勃龙处理LNCaP细胞,既不影响EGF受体的表达,也不影响EGF观察到的增殖反应。使用针对EGF受体的单克隆抗体进行的蛋白质免疫印迹分析显示,DU145细胞裂解物中有一条约170 kD的条带,但用该技术未检测到LNCaP EGF受体。