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高血糖促进前列腺癌细胞中TMPRSS2-ERG基因融合,上调胰岛素样生长因子结合蛋白-2。

Hyperglycemia Promotes TMPRSS2-ERG Gene Fusion in Prostate Cancer Cells Upregulating Insulin-Like Growth Factor-Binding Protein-2.

作者信息

Holly Jeff M P, Broadhurst Jessica, Mansor Rehanna, Bahl Amit, Perks Claire M

机构信息

IGFs & Metabolic Endocrinology Group, School of Clinical Sciences, Southmead Hospital, Bristol, United Kingdom.

Department of Clinical Oncology, Bristol Haematology and Oncology Centre, University Hospitals Bristol, Bristol, United Kingdom.

出版信息

Front Endocrinol (Lausanne). 2017 Nov 6;8:305. doi: 10.3389/fendo.2017.00305. eCollection 2017.

Abstract

BACKGROUND

Epidemiologic evidence shows that obesity is associated with a greater risk of aggressive prostate cancer (PCa) and PCa-specific mortality and this is observed mainly in men with the gene fusion. Obesity is often associated with comorbid conditions such as type 2 diabetes and hyperglycemia: we investigated whether some of the exposures associated with disturbed metabolism can also affect the frequency of this gene fusion.

METHODS

Fusion was induced in LNCaP PCa cells in normal or high levels of glucose, with or without insulin-like growth factor binding protein-2 (IGFBP-2) silenced or the presence of insulin-like growth factor-1 (IGF-I), insulin, or epidermal growth factor (EGF). RNA was extracted for analysis by nested PCR. Abundance of IGFBP-2, γH2AX, DNA-dependent protein kinase catalytic subunit (DNAPKcs), and β-actin were analyzed by Western immunoblotting.

RESULTS

Our data suggest that hyperglycemia-induced IGFBP-2 increased the frequency of the gene fusion that was accompanied by decreased levels of DNAPKcs implying that they were mediated by alterations in the rate of repair of double-strand breaks. In contrast insulin, IGF-I and EGF all decreased gene fusion events.

CONCLUSION

These novel observations may represent a further mechanism by which obesity can exert an effect aggravating PCa progression.

摘要

背景

流行病学证据表明,肥胖与侵袭性前列腺癌(PCa)风险增加及PCa特异性死亡率升高相关,且这一现象主要在携带该基因融合的男性中观察到。肥胖常与2型糖尿病和高血糖等合并症相关:我们研究了一些与代谢紊乱相关的暴露因素是否也会影响该基因融合的频率。

方法

在正常或高糖水平下,对LNCaP前列腺癌细胞诱导融合,同时沉默或不沉默胰岛素样生长因子结合蛋白-2(IGFBP-2),或存在胰岛素样生长因子-1(IGF-I)、胰岛素或表皮生长因子(EGF)。提取RNA用于巢式PCR分析。通过Western免疫印迹分析IGFBP-2、γH2AX、DNA依赖性蛋白激酶催化亚基(DNAPKcs)和β-肌动蛋白的丰度。

结果

我们的数据表明,高血糖诱导的IGFBP-2增加了基因融合频率,同时DNAPKcs水平降低,这意味着它们是由双链断裂修复速率的改变介导的。相反,胰岛素、IGF-I和EGF均降低了基因融合事件。

结论

这些新发现可能代表了肥胖加重PCa进展的另一种机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29a7/5681733/2dce4d43d755/fendo-08-00305-g001a.jpg

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