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从沙蚕中纯化的丝氨酸蛋白酶及其对人肺癌细胞凋亡的影响。

A Purified Serine Protease from Nereis virens and Its Impaction of Apoptosis on Human Lung Cancer Cells.

机构信息

School of Food and Pharmacy, Zhejiang Provincial Engineering Technology Research Center of Marine Biomedical Products, Zhejiang Ocean University, 1st Haidanan Road, Changzhi Island, Lincheng, Zhoushan 316022, China.

Zhejiang Marine Fisheries Research Institution, Zhoushan 316021, China.

出版信息

Molecules. 2017 Jul 7;22(7):1123. doi: 10.3390/molecules22071123.

DOI:10.3390/molecules22071123
PMID:28686182
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6152330/
Abstract

Nereis active protease (NAP) is a novel fibrinolytic active serine protease from the polychaete . In this study, NAP was purified from and the effects of NAP on human lung cancer cells were investigated. Our results indicated that NAP inhibited the proliferation and induced apoptosis of H1299 cells in a time- and dose-dependent manner. The loss of mitochondrial membrane potential, the activation of Bax and cleaved-caspase 3/9, the release of cytochrome C, and the suppression of Bcl-2 and poly-ADP ribose polymerase were observed in NAP-treated H1299 cells by flow cytometry and Western blotting. Moreover, the expression levels of Bax and Bcl-2 mRNA were determined by real-time quantitative polymerase chain reaction and the Bax/Bcl-2 expression ratio was increased in the NAP-treated cell lines. The results indicated that NAP-induced apoptosis may be related to mitochondria mediated apoptosis and occurs through caspase-dependent pathways. Then, the effects of NAP on tumor growth in animal models were observed, where 5 or 10 mg/kg of NAP noticeably reduced tumor volume and weight and increased apoptosis as determined by Western blotting when compared to the negative control group. Therefore, our findings suggest that NAP could be a hopeful anticancer medicine for its propensity to inhibit growth and induce of apoptosis in human lung cancer cells.

摘要

从多毛类环节动物中提取的新型纤维蛋白溶解活性丝氨酸蛋白酶——沙蚕神经活性蛋白酶(NAP)。本研究从沙蚕中提取 NAP,并研究其对人肺癌细胞的影响。结果表明,NAP 呈时间和剂量依赖性抑制 H1299 细胞的增殖并诱导其凋亡。流式细胞术和 Western blot 检测显示,NAP 处理的 H1299 细胞中线粒体膜电位丧失,Bax 和 cleaved-caspase 3/9 激活,细胞色素 C 释放,Bcl-2 和多聚 ADP 核糖聚合酶受到抑制。此外,通过实时定量聚合酶链反应测定 Bax 和 Bcl-2 mRNA 的表达水平,NAP 处理的细胞系中 Bax/Bcl-2 表达比值增加。结果表明,NAP 诱导的细胞凋亡可能与线粒体介导的凋亡有关,并通过 caspase 依赖性途径发生。然后,观察 NAP 对动物模型中肿瘤生长的影响,与阴性对照组相比,5 或 10 mg/kg 的 NAP 可明显降低肿瘤体积和重量,并通过 Western blot 增加凋亡。因此,我们的研究结果表明,NAP 可能成为一种有前途的抗癌药物,因其具有抑制人肺癌细胞生长和诱导细胞凋亡的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dcb/6152330/fbf5c6204113/molecules-22-01123-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dcb/6152330/588563db815e/molecules-22-01123-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dcb/6152330/a24b9a556910/molecules-22-01123-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dcb/6152330/8c4be0c51b8b/molecules-22-01123-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dcb/6152330/05506a4d23e4/molecules-22-01123-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dcb/6152330/6d20a579b5ce/molecules-22-01123-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dcb/6152330/f189c9727168/molecules-22-01123-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dcb/6152330/1fe418c6954f/molecules-22-01123-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dcb/6152330/acaf647ad29f/molecules-22-01123-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dcb/6152330/c7595786077c/molecules-22-01123-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dcb/6152330/fbf5c6204113/molecules-22-01123-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dcb/6152330/588563db815e/molecules-22-01123-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dcb/6152330/a24b9a556910/molecules-22-01123-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dcb/6152330/8c4be0c51b8b/molecules-22-01123-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dcb/6152330/05506a4d23e4/molecules-22-01123-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dcb/6152330/6d20a579b5ce/molecules-22-01123-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dcb/6152330/f189c9727168/molecules-22-01123-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dcb/6152330/1fe418c6954f/molecules-22-01123-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dcb/6152330/acaf647ad29f/molecules-22-01123-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dcb/6152330/c7595786077c/molecules-22-01123-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dcb/6152330/fbf5c6204113/molecules-22-01123-g010.jpg

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