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A549肺癌细胞系对从蚯蚓体腔液中分离出的蛋白多糖复合物Venetin-1的蛋白质组学反应。

Proteomic response of A549 lung cancer cell line to protein-polysaccharide complex Venetin-1 isolated from earthworm coelomic fluid.

作者信息

Czaplewska Paulina, Bogucka Aleksandra, Macur Katarzyna, Rybicka Magda, Rychłowski Michał, Fiołka Marta J

机构信息

Intercollegiate Faculty of Biotechnology, The University of Gdansk, Gdańsk, Poland.

Institute of Biochemistry, Justus Liebig University of Giessen, Giessen, Germany.

出版信息

Front Mol Biosci. 2023 Jun 8;10:1128320. doi: 10.3389/fmolb.2023.1128320. eCollection 2023.

Abstract

Earthworms' celomic fluid has long attracted scientists' interest due to their toxic properties. It has been shown that the elimination of coelomic fluid cytotoxicity to normal human cells was crucial for the generation of the non-toxic Venetin-1 protein-polysaccharide complex, which exhibits selective activity against cells as well as A549 non-small cell lung cancer cells. To find the molecular mechanisms behind the anti-cancer properties of the preparation, this research investigated the proteome response of A549 cells to the presence of Venetin-1. The sequential window acquisition of all theoretical mass spectra (SWATH-MS) methodology was used for the analysis, which allows for a relative quantitative analysis to be carried out without radiolabelling. The results showed that the formulation did not induce significant proteome responses in normal BEAS-2B cells. In the case of the tumour line, 31 proteins were up regulated, and 18 proteins down regulated. Proteins with increased expression in neoplastic cells are mainly associated with the mitochondrion, membrane transport and the endoplasmic reticulum. In the case of altered proteins, Venetin-1 interferes with proteins that stabilise the structures, i.e., keratin, glycolysis/gluconeogenesis and metabolic processes.

摘要

蚯蚓的体腔液因其毒性特性长期以来一直吸引着科学家的关注。研究表明,消除体腔液对正常人类细胞的细胞毒性对于生成无毒的Venetin-1蛋白-多糖复合物至关重要,该复合物对细胞以及A549非小细胞肺癌细胞具有选择性活性。为了探究该制剂抗癌特性背后的分子机制,本研究调查了A549细胞对Venetin-1存在的蛋白质组反应。采用了所有理论质谱的顺序窗口采集(SWATH-MS)方法进行分析,该方法允许在不进行放射性标记的情况下进行相对定量分析。结果表明,该制剂在正常BEAS-2B细胞中未诱导显著的蛋白质组反应。在肿瘤细胞系中,有31种蛋白质上调,18种蛋白质下调。肿瘤细胞中表达增加的蛋白质主要与线粒体、膜转运和内质网有关。在蛋白质发生改变的情况下,Venetin-1会干扰稳定结构的蛋白质,即角蛋白、糖酵解/糖异生和代谢过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20fd/10292018/4d61577d7e03/fmolb-10-1128320-g001.jpg

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