环肽修饰金团簇通过产生细胞内氧化应激诱导肺癌细胞凋亡。

Zhesheng He, Zhongying Du, Chunyu Zhang, Xueyun Gao, Gengmei Xing
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引用次数: 0

摘要

转移性肺癌是癌症患者死亡的主要原因。尽管许多化学药物被开发出来用于治疗癌症,但转移性癌症的死亡率并没有显著下降。本文设计了一种环RGD肽修饰的靶向人肺癌细胞整合素(A549)的Au簇(auc)。rgd - auc能诱导A549细胞凋亡,但对支持呼吸系统的正常细胞支气管上皮细胞(16HBE)无细胞毒性。这些auc可以内化并定位于肿瘤细胞的溶酶体中,并进一步释放到胞浆中。我们发现auc增加了ROS水平,这种高水平的ROS最终导致线粒体去极化。最终,auc刺激线粒体相关凋亡通路,诱导A549肿瘤细胞凋亡。我们推测金簇在未来的研究中将是一种有效的治疗转移性肺肿瘤的候选药物。
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Cyclic Peptide Modified Gold Clusters Induce Lung Tumor Cell Apoptosis via Generating Intracellular Oxidative Stress.

Metastatic lung cancer is the leading cause of death for cancer patients. Although many chemical drugs were developed for cancer treatment, metastatic cancer mortality did not decrease significantly. In this article, we designed an Au clusters (AuCs) modified by cyclic RGD peptides which well target the integrin of human lung carcinoma cells (A549). The RGD-AuCs could well induce A549 cells apoptosis, but have no cytotoxicity on the human bronchial epithelial cells (16HBE), which are normal cells support respiratory system. The AuCs could be internalized and localized in the lysosomes of A549 tumor cells and further release into cytoplasma. We found the ROS level was increased by AuCs, and such high ROS level finally leads to depolarization of mitochondria. Eventually, the AuCs stimulating mitochondria related apoptosis pathway to induce A549 tumor cells apoptosis. We deduce the gold clusters would be an effective therapeutic candidate to against metastatic lung tumor in the future studies.

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来源期刊
Journal of nanoscience and nanotechnology
Journal of nanoscience and nanotechnology 工程技术-材料科学:综合
自引率
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0
审稿时长
3.6 months
期刊介绍: JNN is a multidisciplinary peer-reviewed journal covering fundamental and applied research in all disciplines of science, engineering and medicine. JNN publishes all aspects of nanoscale science and technology dealing with materials synthesis, processing, nanofabrication, nanoprobes, spectroscopy, properties, biological systems, nanostructures, theory and computation, nanoelectronics, nano-optics, nano-mechanics, nanodevices, nanobiotechnology, nanomedicine, nanotoxicology.
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