Martinez Harryl D, Hsiao Jordy J, Jasavala Rohini J, Hinkson Izumi V, Eng Jimmy K, Wright Michael E
University of California Davis Genome Center, University of California at Davis, Davis, CA, USA.
Genes Cancer. 2011 Oct;2(10):956-78. doi: 10.1177/1947601912436422.
Increasing evidence suggests that the disruption of androgen-mediated cellular processes, such as cell proliferation and cell differentiation, contributes to the development of early-stage androgen-dependent prostate cancers. Large-scale mRNA profiling experiments have paved the way in identifying androgen-regulated gene networks that control the proliferation, survival, and differentiation of prostate cancer cells. Despite these extensive research efforts, it remains to be determined whether all androgen-mediated mRNA changes faithfully translate into changes in protein abundance that influence prostate tumorigenesis. Here, we report on a mass spectrometry-based quantitative proteomics analysis that identified known androgen signaling pathways and also novel, androgen-sensitive microsome-associated proteins and protein networks that had not been discovered by gene network studies in human LNCaP prostate cancer cells. Androgen-sensitive microsome-associated proteins encoded components of the insulin growth factor-1 (IGF-1), phosphoinositide 3-kinase (PI3K)/AKT, and extracellular signal-regulated kinase (ERK)/mitogen-activated protein kinase (MAPK) signaling pathways. Further bioinformatic analyses showed most of the androgen-sensitive microsome-associated protein networks play roles in cell proliferation and differentiation. Functional validation experiments showed that the androgen-sensitive microsome-associated proteins Janus kinase 2 (JAK2) and I-kappa B kinase complex-associated protein (IKAP) modulated the expression of prostate epithelial and neuronal markers, attenuated proliferation through an androgen receptor-dependent mechanism, and co-regulated androgen receptor-mediated transcription in LNCaP cells. Further biochemical analyses showed that the increased proliferation in JAK2 knockdown cells was mediated by activation of the mammalian target of rapamycin (mTOR), as determined by increased phosphorylation of several downstream targets (p70 S6 kinase, translational repressor 4E-BP1, and 40S ribosomal S6 protein). We conclude that the expression of microsome-associated proteins that were previously implicated in the tumorigenesis of prostate epithelial cells is strongly influenced by androgens. These findings provide a molecular framework for exploring the mechanisms underlying prostate tumorigenesis and how these protein networks might be attenuated or potentiated in disrupting the growth and survival of human prostate cancers.
越来越多的证据表明,雄激素介导的细胞过程(如细胞增殖和细胞分化)的破坏,促成了早期雄激素依赖性前列腺癌的发展。大规模的mRNA谱分析实验为识别控制前列腺癌细胞增殖、存活和分化的雄激素调节基因网络铺平了道路。尽管进行了这些广泛的研究工作,但仍有待确定是否所有雄激素介导的mRNA变化都能如实地转化为影响前列腺肿瘤发生的蛋白质丰度变化。在此,我们报告了一项基于质谱的定量蛋白质组学分析,该分析鉴定了已知的雄激素信号通路以及新的、雄激素敏感的微粒体相关蛋白和蛋白质网络,这些在人LNCaP前列腺癌细胞的基因网络研究中尚未被发现。雄激素敏感的微粒体相关蛋白编码胰岛素生长因子-1(IGF-1)、磷酸肌醇3-激酶(PI3K)/AKT和细胞外信号调节激酶(ERK)/丝裂原活化蛋白激酶(MAPK)信号通路的成分。进一步的生物信息学分析表明,大多数雄激素敏感的微粒体相关蛋白网络在细胞增殖和分化中发挥作用。功能验证实验表明,雄激素敏感的微粒体相关蛋白Janus激酶2(JAK2)和I-κB激酶复合物相关蛋白(IKAP)调节前列腺上皮和神经元标志物的表达,通过雄激素受体依赖性机制减弱增殖,并在LNCaP细胞中共调节雄激素受体介导的转录。进一步的生化分析表明,JAK2敲低细胞中增殖的增加是由雷帕霉素哺乳动物靶标(mTOR)的激活介导的,这是通过几个下游靶标(p70 S6激酶、翻译抑制因子4E-BP1和40S核糖体S6蛋白)磷酸化的增加来确定的。我们得出结论,先前与前列腺上皮细胞肿瘤发生有关的微粒体相关蛋白的表达受到雄激素的强烈影响。这些发现为探索前列腺肿瘤发生的潜在机制以及这些蛋白质网络在破坏人类前列腺癌的生长和存活中如何被减弱或增强提供了一个分子框架。