首页> 外文期刊>Molecular Carcinogenesis >G Cryptotanshinone, a Novel Tumor Angiogenesis Inhibitor, Destabilizes Tumor Necrosis Factor-alpha mRNA Via Decreasing Nuclear-Cytoplasmic Translocation of RNA-Binding Protein HuR
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G Cryptotanshinone, a Novel Tumor Angiogenesis Inhibitor, Destabilizes Tumor Necrosis Factor-alpha mRNA Via Decreasing Nuclear-Cytoplasmic Translocation of RNA-Binding Protein HuR

机译:G隐丹参酮,一种新型的肿瘤血管生成抑制剂,通过减少RNA结合蛋白HuR的核细胞质易位,使肿瘤坏死因子-αmRNA不稳定。

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摘要

Cryptotanshinone (CT), one major lipophilic component isolated from Salvia miltiorrhiza Bunge, has shown to possess chemopreventive properties against various types of cancer cells. In this study, CT was shown to be a potent antiangiogenic agent in zebrafish, and mouse models and could limit tumor growth by inhibiting tumor angiogenesis. We further found that CT could inhibit the proliferation, migration, angiogenic sprouting, and tube formation of HUVECs. In addition, we demonstrated that CT could lower the level of TNF-alpha due to the destabilization of TNF-alpha mRNA, which associated with regulating 3'-untranslated region (3'-UTR) of TNF-alpha and preventing the translocation of RNA binding protein, HuR, from the nucleus to the cytoplasm. Moreover, the underlying mechanism responsible for the regulation in angiogenesis by CT was partially related to the suppression of NF-kappa B, and STAT3 activity. Based on the abilities of CT in targeting tumor cells, inhibiting angiogenesis, and destroying tumor vasculature, CT is worthy of further investigation for preventive, and therapeutic purposes in cancer. (C) 2015 Wiley Periodicals, Inc.
机译:隐丹参酮(CT)是从丹参丹参中分离出的一种主要的亲脂性成分,已显示出对各种类型癌细胞的化学预防特性。在这项研究中,CT被证明是斑马鱼和小鼠模型中的一种有效的抗血管生成剂,并且可以通过抑制肿瘤血管生成来限制肿瘤的生长。我们进一步发现CT可以抑制HUVEC的增殖,迁移,血管新生和管形成。此外,我们证明CT可以降低TNF-alpha的水平,这是由于TNF-alpha的失稳,这与调节TNF-alpha的3'-非翻译区(3'-UTR)和防止RNA易位有关从细胞核到细胞质的结合蛋白HuR。此外,由CT调节血管生成的潜在机制部分与NF-κB和STAT3活性的抑制有关。基于CT靶向肿瘤细胞,抑制血管生成和破坏肿瘤脉管系统的能力,CT在癌症的预防和治疗目的方面值得进一步研究。 (C)2015威利期刊公司

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