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首页> 外文期刊>The Prostate >Antiandrogenic and growth inhibitory effects of ring-substituted analogs of 3,3'-diindolylmethane (ring-DIMs) in hormone-responsive LNCaP human prostate cancer cells.
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Antiandrogenic and growth inhibitory effects of ring-substituted analogs of 3,3'-diindolylmethane (ring-DIMs) in hormone-responsive LNCaP human prostate cancer cells.

机译:3,3'-二吲哚甲烷(ring-DIM)的环取代类似物在激素反应性LNCaP人前列腺癌细胞中的抗雄激素作用和生长抑制作用。

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BACKGROUND: Cruciferous vegetables protect against prostate cancer. Indole-3-carbinol (I3C) and its major metabolite 3,3'-diindolylmethane (DIM), exhibit antitumor activities in vitro and in vivo. Several synthetic ring-substituted dihaloDIMs (ring-DIMs) appear to have increased anticancer activity. METHODS: Inhibition of LNCaP prostate cancer cell growth was measured by a WST-1 cell viability assay. Cytoplasmic and nuclear proteins were analyzed by immunoblotting and immunofluorescence. Androgen receptor (AR) activation was assessed by measuring prostate-specific antigen (PSA) expression and using LNCaP cells containing human AR and an AR-dependent probasin promoter-green fluorescent protein (GFP) construct. RESULTS: Like DIM, several ring-substituted dihaloDIM analogs, namely 4,4'-dibromo-, 4,4'-dichloro-, 7,7'-dibromo-, and 7,7'-dichloroDIM, significantly inhibited DHT-stimulated growth of LNCaP cells at concentrations >/=1 microM. We observed structure-dependent differences for the effects of the ring-DIMs on AR expression, nuclear AR accumulation and PSA levels in LNCaP cells after 24 hr. Both 4,4'- and 7,7'-dibromoDIM decreased AR protein and mRNA levels, whereas 4,4'- and 7,7'-dichloroDIM had minimal effect. All four dihaloDIMs (10 and 30 microM) significantly decreased PSA protein and mRNA levels. Immuofluorescence studies showed that only the dibromoDIMs increased nuclear localization of AR. All ring-DIMs caused a concentration-dependent decrease in fluorescence induced by the synthetic androgen R1881 in LNCaP cells transfected with wild-type human AR and an androgen-responsive probasin promoter-GFP gene construct, with potencies up to 10-fold greater than that of DIM. CONCLUSION: The antiandrogenic effects of ring-DIMs suggest they may form the basis for the development of novel agents against hormone-sensitive prostate cancer, alone or in combination with other drugs.
机译:背景:十字花科蔬菜可预防前列腺癌。吲哚-3-甲醇(I3C)及其主要代谢物3,3'-二吲哚基甲烷(DIM)在体外和体内均表现出抗肿瘤活性。几种合成的环取代的二卤代DIM(ring-DIM)似乎具有增强的抗癌活性。方法:通过WST-1细胞活力测定法测定对LNCaP前列腺癌细胞生长的抑制作用。通过免疫印迹和免疫荧光分析细胞质和核蛋白。通过测量前列腺特异性抗原(PSA)的表达并使用含有人AR和依赖AR的前列腺素启动子-绿色荧光蛋白(GFP)构建物的LNCaP细胞,评估雄激素受体(AR)的激活。结果:与DIM一样,几种环取代的dihaloDIM类似物,即4,4'-dibromo-,4,4'-dichloro-,7,7'-dibromo-和7,7'-dichloroDIM,显着抑制DHT刺激。浓度> / = 1 microM时LNCaP细胞的生长。我们观察到环DIM对AR表达,核AR积累和LNCaP细胞中PSA水平24小时后影响的结构依赖性差异。 4,4'-和7,7'-dibromoDIM均可降低AR蛋白和mRNA水平,而4,4'-和7,7'-dichloroDIM的作用则很小。所有四个dihaloDIM(10和30 microM)均显着降低PSA蛋白和mRNA水平。免疫荧光研究表明,只有dibromoDIM会增加AR的核定位。所有环-DIM都导致在野生型人AR和雄激素反应性probasin启动子-GFP基因构建体转染的LNCaP细胞中,由合成雄激素R1881诱导的荧光浓度依赖性降低,其效力比后者高10倍DIM。结论:环-DIMs的抗雄激素作用表明,它们可能构成单独或与其他药物联合使用的抗激素敏感性前列腺癌新药开发的基础。

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