过氧化氢酶
肿瘤缺氧
放射治疗
免疫系统
蛋白酶
体内
癌症研究
化学
药理学
缺氧(环境)
生物
细胞生物学
酶
生物化学
免疫学
氧气
医学
内科学
生物技术
有机化学
作者
Wenjing Zai,Lin Kang,Tiejun Dong,Haoran Wang,Lining Yin,Shaoju Gan,Wenjia Lai,Yibing Ding,Yiqiao Hu,Jinhui Wu
出处
期刊:ACS Nano
[American Chemical Society]
日期:2021-09-14
卷期号:15 (9): 15381-15394
被引量:52
标识
DOI:10.1021/acsnano.1c07621
摘要
Hypoxia is one of the most important factors that limit the effect of radiotherapy, and the abundant H2O2 in tumor tissues will also aggravate hypoxia-induced radiotherapy resistance. Delivering catalase to decompose H2O2 into oxygen is an effective strategy to relieve tumor hypoxia and radiotherapy resistance. However, low stability limits catalase's in vivo application, which is one of the most common limitations for almost all proteins' internal utilization. Here, we develop catalase containing E. coli membrane vesicles (EMs) with excellent protease resistance to relieve tumor hypoxia for a long time. Even treated with 100-fold of protease, EMs showed higher catalase activity than free catalase. After being injected into tumors post 12 h, EMs maintained their hypoxia relief ability while free catalase lost its activity. Our results indicate that EMs might be an excellent catalase delivery for tumor hypoxia relief. Combined with their immune stimulation features, EMs could enhance radiotherapy and induce antitumor immune memory effectively.
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