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缺氧诱导的血管生成素样蛋白4作为人类前列腺癌的临床生物标志物和治疗靶点

Hypoxia-induced angiopoietin-like protein 4 as a clinical biomarker and treatment target for human prostate cancer.

作者信息

Hata Shinro, Nomura Takeo, Iwasaki Kazunori, Sato Ryuta, Yamasaki Mutsushi, Sato Fuminori, Mimata Hiromitsu

机构信息

Department of Urology, Oita University Faculty of Medicine, Yufu, Oita 879-5593, Japan.

出版信息

Oncol Rep. 2017 Jul;38(1):120-128. doi: 10.3892/or.2017.5669. Epub 2017 May 24.

Abstract

Angiopoietin-like protein 4 (ANGPTL4) is a multifunctional protein, playing roles in glucose and lipid metabolism, inflammation, angiogenesis, and tumorigenesis. Recent research suggests that ANGPTL4 is induced by hypoxia and is a useful diagnostic or prognostic marker for various cancers. However, it remains unclear whether ANGPTL4 expression influences prostate cancer. Here we examined the biological and clinical relevance of ANGPTL4 expression in prostate cancer. Firstly we examined ANGPTL4 expression in the prostate cancer cell lines LNCaP and LNCaP/CH incubated at 1% O2 for at least 6 months. We compared cellular proliferation, migration, and ANGPTL4 secretion in a culture medium between these cell lines. In addition, we investigated the effect of various concentrations of recombinant ANGPTL4 protein (rANGPTL4) on cellular proliferation and intracellular signaling pathways. Moreover, we used ANGPTL4 knockdown by RNA interference to investigate the influence of ANGPTL4 expression on these cell lines. Finally, we investigated the correlation between ANGPTL4 expression in prostate cancer specimens and clinicopathological parameters using immunohistochemistry. Our data suggested that the expression of ANGPTL4 in hypoxic conditions was 14.4-fold higher than that in normoxic condition. ANGPTL4 secretion in the culture medium increased 7.0-fold. In addition, rANGPTL4 increased cellular proliferation 1.72-fold via Akt activation. Moreover, ANGPTL4 knockdown decreased cell growth and its secretion by 25.7 and 41.4%, respectively, compared with the control. A multivariate analysis showed that positive ANGPTL4 expression in the resected specimens was an independent prognostic indicator of biochemical recurrence (P=0.03, hazard ratio = 2.02). Our results show that ANGPTL4 is induced by hypoxia and promotes cancer progression via the activated PI3K/Akt pathway. Moreover, ANGPTL4 can be used as a prognostic marker for prostate cancer patients undergoing radical prostatectomy.

摘要

血管生成素样蛋白4(ANGPTL4)是一种多功能蛋白,在葡萄糖和脂质代谢、炎症、血管生成及肿瘤发生过程中发挥作用。近期研究表明,ANGPTL4由缺氧诱导产生,是多种癌症有用的诊断或预后标志物。然而,ANGPTL4表达是否影响前列腺癌仍不清楚。在此,我们研究了ANGPTL4表达在前列腺癌中的生物学及临床相关性。首先,我们检测了在1%氧气条件下培养至少6个月的前列腺癌细胞系LNCaP和LNCaP/CH中ANGPTL4的表达。我们比较了这些细胞系在培养基中的细胞增殖、迁移及ANGPTL4分泌情况。此外,我们研究了不同浓度的重组ANGPTL4蛋白(rANGPTL4)对细胞增殖及细胞内信号通路的影响。而且,我们利用RNA干扰敲低ANGPTL4,以研究ANGPTL4表达对这些细胞系的影响。最后,我们采用免疫组织化学方法研究前列腺癌标本中ANGPTL4表达与临床病理参数之间的相关性。我们的数据表明,缺氧条件下ANGPTL4的表达比常氧条件下高14.4倍。培养基中ANGPTL4的分泌增加了7.0倍。此外,rANGPTL通过激活Akt使细胞增殖增加1.72倍。而且,与对照组相比,敲低ANGPTL4分别使细胞生长及其分泌减少了25.7%和41.4%。多因素分析显示,切除标本中ANGPTL4阳性表达是生化复发的独立预后指标(P = 0.03,风险比=2.02)。我们的结果表明,ANGPTL4由缺氧诱导产生,并通过激活PI3K/Akt途径促进癌症进展。此外,ANGPTL4可作为接受根治性前列腺切除术的前列腺癌患者的预后标志物。

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