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腺病毒介导的核心蛋白聚糖表达通过激活p53和线粒体凋亡诱导癌细胞死亡。

Adenovirus-mediated decorin expression induces cancer cell death through activation of p53 and mitochondrial apoptosis.

作者信息

Yoon A-Rum, Hong JinWoo, Yun Chae-Ok

机构信息

Department of Bioengineering, College of Engineering, Hanyang University, Seongdong-gu, Seoul 04763, Korea.

出版信息

Oncotarget. 2017 Sep 8;8(44):76666-76685. doi: 10.18632/oncotarget.20800. eCollection 2017 Sep 29.

DOI:10.18632/oncotarget.20800
PMID:29100340
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5652734/
Abstract

Decorin (DCN) is a small leucine-rich proteoglycan that plays an important role in the regulation of apoptosis, proliferation, intercellular contact, and cell migration. Here we have investigated the detailed mechanism of apoptotic cell death induced by DCN expression. A marked increase in cytotoxicity was observed for both DCN-expressing replication-incompetent (dE1/DCN) and -competent (dB/DCN) adenoviruses (Ads) compared to the corresponding control Ads. FACS and TUNEL assays revealed that the expression of DCN induced apoptotic cell death. Specifically, the expression and stability of p53 were increased by DCN. In addition, western blot data showed that DCN expression activated mitochondrial apoptosis by increasing the expression level of p53. Similarly, DCN-expressing oncolytic Ads induced a greater antitumor effect in a murine xenograft model compared with control Ads. Tissue staining and western blot data from experiments demonstrated significantly higher levels of apoptosis in tumor tissues from mice treated with DCN-expressing Ads compared to those treated with control Ads. Collectively, these data support that cell killing effect is enhanced with Ad-mediated DCN expression via the induction of p53-mediated mitochondrial apoptosis, which could be a valuable benefit for antitumor efficacy.

摘要

核心蛋白聚糖(DCN)是一种富含亮氨酸的小分子蛋白聚糖,在细胞凋亡、增殖、细胞间接触和细胞迁移的调节中发挥重要作用。在此,我们研究了DCN表达诱导凋亡性细胞死亡的详细机制。与相应的对照腺病毒(Ads)相比,表达DCN的无复制能力(dE1/DCN)和有复制能力(dB/DCN)的腺病毒均观察到细胞毒性显著增加。流式细胞术(FACS)和TUNEL分析表明,DCN的表达诱导了凋亡性细胞死亡。具体而言,DCN增加了p53的表达和稳定性。此外,蛋白质印迹数据显示,DCN表达通过增加p53的表达水平激活了线粒体凋亡。同样,与对照Ads相比,表达DCN的溶瘤腺病毒在小鼠异种移植模型中诱导了更大的抗肿瘤作用。实验的组织染色和蛋白质印迹数据表明,与用对照Ads处理的小鼠相比,用表达DCN的Ads处理的小鼠肿瘤组织中的凋亡水平显著更高。总体而言,这些数据支持通过诱导p53介导的线粒体凋亡,Ad介导的DCN表达增强了细胞杀伤作用,这可能对抗肿瘤疗效具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79f6/5652734/445600c27f95/oncotarget-08-76666-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79f6/5652734/4ca0068e2f5c/oncotarget-08-76666-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79f6/5652734/445600c27f95/oncotarget-08-76666-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79f6/5652734/4ca0068e2f5c/oncotarget-08-76666-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79f6/5652734/b59eab82c79a/oncotarget-08-76666-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79f6/5652734/dd335046b406/oncotarget-08-76666-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79f6/5652734/cdb7bb519953/oncotarget-08-76666-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79f6/5652734/eba20659ec5f/oncotarget-08-76666-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79f6/5652734/eec3c47c093e/oncotarget-08-76666-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79f6/5652734/445600c27f95/oncotarget-08-76666-g007.jpg

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Recombinant human decorin suppresses liver HepG2 carcinoma cells by p21 upregulation.
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Engineered smart materials for RNA based molecular therapy to treat Glioblastoma.用于基于RNA的分子疗法治疗胶质母细胞瘤的工程智能材料。
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Prognostic analysis of tumor mutation burden and immune infiltration in hepatocellular carcinoma based on TCGA data.基于 TCGA 数据的肝癌肿瘤突变负荷和免疫浸润的预后分析。
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