Stimulus-activated ribonuclease targeting chimeras for tumor microenvironment activated cancer therapy

被引:0
|
作者
Zhang, Yuqi [1 ,2 ]
Zhu, Jinfeng [3 ]
Qiu, Ling [4 ]
Lv, Zhengzhong [1 ,2 ]
Zhao, Zhongsheng [1 ,2 ]
Ren, Xingxiang [1 ,2 ]
Guo, Yirui [1 ,2 ]
Chen, Yan [1 ,2 ]
Li, Miao [1 ,2 ]
Fan, Yurong [5 ]
Han, Zhixin [1 ,2 ]
Feng, Yiming [1 ,2 ]
Shi, Haibin [1 ,2 ]
机构
[1] Soochow Univ, Sch Radiat Med & Protect, State Key Lab Radiat Med & Protect, Suzhou, Peoples R China
[2] Soochow Univ, Collaborat Innovat Ctr Radiol Med Jiangsu Higher E, Suzhou, Peoples R China
[3] Univ Roma Tor Vergata, Dept Expt Med, Rome, Italy
[4] Minist Hlth, Jiangsu Inst Nucl Med, Key Lab Nucl Med, Jiangsu Key Lab Mol Nucl Med, Wuxi, Peoples R China
[5] Soochow Univ, Affiliated Hosp 2, Dept Radiol, Suzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
RNA INTERFERENCE; SUPPRESSOR; MODEL;
D O I
10.1038/s41467-025-56691-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
RNA degradation using ribonuclease targeting chimeras (RiboTACs) is a promising approach for cancer therapy. However, potential off-target degradation is a serious issue. Here, a RiboTAC is designed for tumor microenvironment triggered activation. The tumor microenvironment activated RiboTAC (TaRiboTAC) incorporates two pre-miR-21 binders, a near-infrared fluorophore IR780, an RGD targeting peptide and a phenylboronic acid caged ribonuclease recruiter. The caged ribonuclease recruiter is embedded in the molecule and exposed in acidic pH, the phenylboronic acid cage is removed by H2O2 making the TaRiboTAC responsive to the acidic and high H2O2 levels in the tumor microenvironment. It is shown the TaRiboTAC targets tumor tissue and degrades pre-miR-21. The degradation of pre-miR-21 by TaRiboTACs significantly increases the radiotherapeutic susceptibility of cancer cells achieving efficient suppression of human lung adenocarcinoma A549 tumors in living mice.
引用
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页数:15
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