Sekine Yoshitaka, Osei-Hwedieh David, Matsuda Kant, Raghavachari Nalini, Liu Delong, Furuya Yosuke, Koike Hidekazu, Suzuki Kazuhiro, Remaley Alan T
Lipoprotein Metabolism Section, Pulmonary and Vascular Medicine Branch, NHLBI, National Institutes of Health, Bethesda, Maryland; Department of Urology, Gunma University Graduate School of Medicine, Maebashi, Gunma, Japan.
Prostate. 2011 Oct 1;71(14):1499-509. doi: 10.1002/pros.21365. Epub 2011 Mar 3.
High fat diets are known to be a risk factor for prostate cancer. In this study, we investigated the effect of high fat diet on mouse prostate gene expression.
C57BL/6J mice were fed either a control or high fat diet for 12 weeks. Microarray analyses were performed on mouse ventral prostate (VP) and dorsolateral prostate (DLP), followed by canonical pathway analysis and regulatory network identification. mRNA changes were confirmed by real time PCR.
Approximately 2,125, and 1,194 genes responded significantly to the high fat diet in VP, DLP, respectively. Pathways and networks related to oxidative stress, glutathione metabolism, NRF-mediated oxidative stress response and NF-kappaB were all differentially regulated by high fat diet. Glutathione peroxidase 3 (GPx3) mRNA levels were decreased by approximately twofold by high fat diet in all three prostate lobes. In human non-transformed prostate cells (PrSC, PrEC, and BPH-1), cholesterol loading decreased GPx3 expression, and increased H2 O2 levels of culture medium. Troglitazone increased GPx3 expression in three normal prostate cells, and decreased H2 O2 levels. In addition, troglitazone attenuated cholesterol-induced H2 O2 increase. Tissue from prostate cancer biopsies had decreased GPx3 mRNA and its level was inversely related to the Gleason score.
High fat diet alters pathways related to many genes concerned with oxidative stress. GPx3, a gene identified by this analysis, was found to be down-regulated by high fat diet and appears be decreased in human prostate cancers, suggesting that GPx3 may have a possible role in modulating carcinogenesis. Prostate 71:1499-1509, 2011. © 2011 Wiley-Liss, Inc.
高脂肪饮食是前列腺癌的已知危险因素。在本研究中,我们调查了高脂肪饮食对小鼠前列腺基因表达的影响。
将C57BL/6J小鼠分别喂食对照饮食或高脂肪饮食12周。对小鼠腹侧前列腺(VP)和背外侧前列腺(DLP)进行微阵列分析,随后进行经典通路分析和调控网络鉴定。通过实时PCR确认mRNA变化。
在VP和DLP中,分别约有2,125个和1,194个基因对高脂肪饮食有显著反应。与氧化应激、谷胱甘肽代谢、NRF介导的氧化应激反应和NF-κB相关的通路和网络均受到高脂肪饮食的差异调节。在所有三个前列腺叶中,高脂肪饮食使谷胱甘肽过氧化物酶3(GPx3)mRNA水平降低了约两倍。在人未转化的前列腺细胞(PrSC、PrEC和BPH-1)中,胆固醇加载降低了GPx3表达,并增加了培养基中的H2O2水平。曲格列酮增加了三种正常前列腺细胞中的GPx3表达,并降低了H2O2水平。此外,曲格列酮减弱了胆固醇诱导的H2O2增加。前列腺癌活检组织中的GPx3 mRNA减少,其水平与Gleason评分呈负相关。
高脂肪饮食改变了与许多氧化应激相关基因有关的通路。通过本分析鉴定的基因GPx3被发现受高脂肪饮食下调,并且在人类前列腺癌中似乎减少,这表明GPx3可能在调节致癌作用中发挥作用。前列腺71:1499 - 1509, 2011。© 2011威利 - 利斯公司。