Plecstatin-1诱导结直肠肿瘤球状体†的免疫原性细胞死亡标志

IF 2.9 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Metallomics Pub Date : 2020-12-09 DOI:10.1039/D0MT00227E
Debora Wernitznig, Samuel M. Meier-Menches, Klaudia Cseh, Sarah Theiner, Dominik Wenisch, Andreas Schweikert, Michael A. Jakupec, Gunda Koellensperger, Andreas Wernitznig, Wolfgang Sommergruber and Bernhard K. Keppler
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引用次数: 20

摘要

有机金属(芳烃)抗癌剂被认为对潜在的细胞靶点具有低选择性。然而,钌(芳烃)吡啶碳硫酰胺(plecstatin-1)对plectin(一种支架蛋白和细胞连接物)表现出靶向选择性。我们采用了一个三维肿瘤球体模型,发现plecstatin-1通过破坏细胞骨架组织,限制了球体的生长,诱导了肿瘤球体的形态和结构的变化。此外,我们证明plecstatin-1诱导氧化应激,随后通过eIF2α磷酸化,暴露钙网蛋白,HSP90和HSP70在细胞膜上,分泌ATP,然后释放高迁移率组盒1,诱导免疫原性细胞死亡信号。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Plecstatin-1 induces an immunogenic cell death signature in colorectal tumour spheroids†

Plecstatin-1 induces an immunogenic cell death signature in colorectal tumour spheroids†

Organometallic metal(arene) anticancer agents were believed to confer low selectivity for potential cellular targets. However, the ruthenium(arene) pyridinecarbothioamide (plecstatin-1) showed target selectivity for plectin, a scaffold protein and cytolinker. We employed a three-dimensional cancer spheroid model and showed that plecstatin-1 limited spheroid growth, induced changes in the morphology and in the architecture of tumour spheroids by disrupting the cytoskeletal organization. Additionally, we demonstrated that plecstatin-1 induced oxidative stress, followed by the induction of an immunogenic cell death signature through phosphorylation of eIF2α, exposure of calreticulin, HSP90 and HSP70 on the cell membrane and secretion of ATP followed by release of high mobility group box-1.

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来源期刊
Metallomics
Metallomics 生物-生化与分子生物学
CiteScore
7.00
自引率
5.90%
发文量
87
审稿时长
1 months
期刊介绍: Global approaches to metals in the biosciences
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