Suppr超能文献

岩藻黄质通过PI3K/Akt信号通路诱导人宫颈癌细胞系HeLa凋亡。

Fucoxanthin induces apoptosis in human cervical cancer cell line HeLa via PI3K/Akt pathway.

作者信息

Ye Guoliu, Lu Qin, Zhao Weidong, Du Danli, Jin Lijie, Liu Yusheng

机构信息

Department of Obstetrics and Gynecology, Provincial Hospital, Affiliated to Anhui Medical University, Hefei, 230001, China.

出版信息

Tumour Biol. 2014 Nov;35(11):11261-7. doi: 10.1007/s13277-014-2337-7. Epub 2014 Aug 13.

Abstract

Cervical cancer (CC) is a malignant neoplasm arising from cells originating in the cervix uteri, among the top causes of death from cancer in women. In a gene expression profiling study of metabolic response to treatment, PI3K/Akt signaling pathway are associated with the development of CC. A common mechanism of Akt activation seen in cancer types is alterations in the upstream regulators of Akt such as phosphatidylinositol 3-kinase (PI3K), which is overexpressed in cervical cancer tissues, and leads to phosphorylation of Akt. Both PI3K and Akt inhibitors exist and may be therapeutically valuable. In the present study, we use MTT assay and western blot for the high-throughput screening to select specific inhibitors of PI3K/Akt signaling pathway, and then obtain fucoxanthin. Fucoxanthin is a water-soluble dietary fiber, taken from the unique slimy component of alginic cells. Various studies have pointed out that fucoxanthin is very effective for the treatment of cancer. Our results have shown that fucoxanthin induced a significant apoptosis of HeLa cells, compared with other candidates. After treatment with fucoxanthin for 24 h, the level of phosphorylation was inhibited in a dose-dependent manner, and the proteins of apoptotic markers were changed in HeLa cells. And fucoxanthin could suppress tumor growth in vivo. In addition, the mitochondrial signal transduction pathway maybe was involved in its mechanism and NF-κB activation was decreased after treatment with fucoxanthin. Therefore, fucoxanthin may be used as anti-cervical cancer drugs in the future.

摘要

宫颈癌(CC)是一种起源于子宫颈细胞的恶性肿瘤,是女性癌症死亡的主要原因之一。在一项关于治疗代谢反应的基因表达谱研究中,PI3K/Akt信号通路与宫颈癌的发生发展相关。在多种癌症类型中常见的Akt激活机制是其上游调节因子如磷脂酰肌醇3激酶(PI3K)发生改变,PI3K在宫颈癌组织中过表达,导致Akt磷酸化。PI3K和Akt抑制剂均已存在,且可能具有治疗价值。在本研究中,我们使用MTT法和蛋白质印迹法进行高通量筛选以选择PI3K/Akt信号通路的特异性抑制剂,进而获得了岩藻黄质。岩藻黄质是一种水溶性膳食纤维,取自藻类细胞独特的黏液成分。多项研究指出,岩藻黄质对癌症治疗非常有效。我们的结果表明,与其他候选物相比,岩藻黄质可诱导HeLa细胞发生显著凋亡。用岩藻黄质处理24小时后,HeLa细胞中的磷酸化水平呈剂量依赖性受到抑制,凋亡标志物蛋白发生改变。并且岩藻黄质可在体内抑制肿瘤生长。此外,其作用机制可能涉及线粒体信号转导通路,用岩藻黄质处理后NF-κB激活减少。因此,岩藻黄质未来可能用作抗宫颈癌药物。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验