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人前列腺癌中过度表达泛素样分子干扰素刺激基因 15。

The ubiquitin-like molecule interferon-stimulated gene 15 is overexpressed in human prostate cancer.

机构信息

Department of Urology, Kochi Medical School, Kochi University, Nankoku, Kochi, Japan.

出版信息

Oncol Rep. 2010 Jan;23(1):11-6.

Abstract

To identify molecules to serve as diagnostic markers for high-grade prostate cancer (PC) and targets for novel therapeutic drugs, we investigated the gene expression profiles of high-grade PCs using a cDNA microarray combined with laser microbeam microdissection. We subsequently confirmed that the ubiquitin-like molecule interferon-stimulated gene 15 (ISG15) was expressed exclusively in high-grade PCs with high Gleason scores. Semi-quantitative reverse transcription PCR and immunohistochemical analysis confirmed the overexpression of ISG15, a 165 amino acid interferon-inducible ubiquitin-like protein, specifically in high-grade PCs with high Gleason scores 8-9, while it was not expressed in the normal prostate. Immunohistochemical analysis using anti-ISG15 polyclonal antibody confirmed an elevated expression of ISG15 protein in high-grade PCs as well as low-grade PCs compared with that in normal prostate (NP) epithelium. Knockdown of ISG15 expression by short interfering RNA (siRNA) in a PC cell line resulted in marked attenuation of PC cell survival; concordantly, ISG15 overexpression in a PC cell line promoted PC cell growth, indicating its oncogenic property. These findings suggest that ISG15 is involved in cell growth and survival of PCs and that it could be a potential molecular target for new therapeutics and a diagnostic biomarker for human PCs.

摘要

为了鉴定可作为高级别前列腺癌(PC)诊断标志物和新型治疗药物靶点的分子,我们使用 cDNA 微阵列结合激光微束显微切割技术,研究了高级别 PC 的基因表达谱。随后,我们证实泛素样分子干扰素刺激基因 15(ISG15)仅在高评分的高级别 PC 中表达。半定量逆转录 PCR 和免疫组织化学分析证实,ISG15(一种 165 个氨基酸的干扰素诱导的泛素样蛋白)在高评分 8-9 的高级别 PC 中特异性过表达,而在正常前列腺中不表达。使用抗 ISG15 多克隆抗体的免疫组织化学分析证实,与正常前列腺(NP)上皮相比,ISG15 蛋白在高级别和低级别 PC 中的表达升高。在 PC 细胞系中通过短发夹 RNA(siRNA)敲低 ISG15 的表达会导致 PC 细胞存活明显减弱;相反,在 PC 细胞系中过表达 ISG15 会促进 PC 细胞生长,表明其具有致癌性。这些发现表明,ISG15 参与 PC 细胞的生长和存活,可能是新型治疗方法的潜在分子靶点和人类 PC 的诊断生物标志物。

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