One-shot dual gene editing for drug-resistant pancreatic cancer therapy

被引:11
作者
Won, Eun-Jeong [1 ]
Park, Hyeji [2 ]
Chang, Seung-Hee [1 ,4 ]
Kim, Jin Hyun [1 ,4 ]
Kwon, Hojeong [3 ]
Cho, Young-Seok [2 ]
Yoon, Tae-Jong [1 ,4 ]
机构
[1] Ajou Univ, Res Inst Pharmaceut Sci & Technol RIPST, Coll Pharm, Lab Nanopharm, Suwon, South Korea
[2] Catholic Univ Korea, Coll Med, Seoul St Marys Hosp, Dept Internal Med, Seoul 06591, South Korea
[3] NYU, Coll Arts & Sci, Dept Anthropol, New York, NY USA
[4] Moogene Medi Inst, Korea Bio Pk, Seongnam, South Korea
关键词
Nanoliposome; Gene editing; Drug-resistance; Pancreatic cancer; Protein delivery; ONCOGENIC KRAS; GEMCITABINE RESISTANCE; CELLS; METABOLISM; INCREASES; DELIVERY;
D O I
10.1016/j.biomaterials.2021.121252
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
It is challenging to diagnose patients with pancreatic ductal adenocarcinoma (PDAC) early on, and their treat-ment is often complex. Gemcitabine (GEM) is the first-line treatment for PDAC, but its efficacy is limited in most patients due to the GEM resistance from KRAS and P53 gene mutations. We describe the correction of a double gene mutation and therapeutic effect for the GEM resistant PDAC. Bio-available nanoliposomes (NL) possessing Cas9-ribonucleoproteins and adenine-base editors were developed to conduct KRAS and P53 mutation gene editing directly. NLs were conjugated with EGFR antibodies to tumor-specific delivery, and the anti-cancer effect was verified in vitro and in vivo Model. Our GEM-combinatorial therapeutic strategies using double gene editing systems with one-shot may be a potent therapy for PDAC, overcoming chemoresistance.
引用
收藏
页数:10
相关论文
共 36 条
[1]   Gemcitabine resistance in pancreatic ductal adenocarcinoma [J].
Binenbaum, Yoav ;
Na'ara, Shorook ;
Gil, Ziv .
DRUG RESISTANCE UPDATES, 2015, 23 :55-68
[2]   Spatiotemporal Delivery of CRISPR/Cas9 Genome Editing Machinery Using Stimuli-Responsive Vehicles [J].
Cai, Weiqi ;
Luo, Tianli ;
Mao, Lanqun ;
Wang, Ming .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2021, 60 (16) :8596-8606
[3]  
Cavalcante LD, 2014, EUR J PHARMACOL, V741, P8, DOI [10.1010/j.ejphar.2014.07.041, 10.1016/j.ejphar.2014.07.041]
[4]   Oncogenic Kras is required for both the initiation and maintenance of pancreatic cancer in mice [J].
Collins, Meredith A. ;
Bednar, Filip ;
Zhang, Yaqing ;
Brisset, Jean-Christophe ;
Galban, Stefanie ;
Galban, Craig J. ;
Rakshit, Sabita ;
Flannagan, Karen S. ;
Adsay, N. Volkan ;
di Magliano, Marina Pasca .
JOURNAL OF CLINICAL INVESTIGATION, 2012, 122 (02) :639-653
[5]   Programmable base editing of A.T to G.C in genomic DNA without DNA cleavage [J].
Gaudelli, Nicole M. ;
Komor, Alexis C. ;
Rees, Holly A. ;
Packer, Michael S. ;
Badran, Ahmed H. ;
Bryson, David I. ;
Liu, David R. .
NATURE, 2017, 551 (7681) :464-+
[6]   High levels of AAV vector integration into CRISPR-induced DNA breaks [J].
Hanlon, Killian S. ;
Kleinstiver, Benjamin P. ;
Garcia, Sara P. ;
Zaborowski, Mikolaj P. ;
Volak, Adrienn ;
Spirig, Stefan E. ;
Muller, Alissa ;
Sousa, Alexander A. ;
Tsai, Shengdar Q. ;
Bengtsson, Niclas E. ;
Loov, Camilla ;
Ingelsson, Martin ;
Chamberlain, Jeffrey S. ;
Corey, David P. ;
Aryee, Martin J. ;
Joung, J. Keith ;
Breakefield, Xandra O. ;
Maguire, Casey A. ;
Gyorgy, Bence .
NATURE COMMUNICATIONS, 2019, 10 (1)
[7]   Functional repair of p53 mutation in colorectal cancer cells using trans-splicing [J].
He, Xingxing ;
Liao, Jiazhi ;
Liu, Fang ;
Yan, Junwei ;
Yan, Jingjun ;
Shang, Haitao ;
Dou, Qian ;
Chang, Ying ;
Lin, Jusheng ;
Song, Yuhu .
ONCOTARGET, 2015, 6 (04) :2034-2045
[8]   FBW7 increases the chemosensitivity of pancreatic cancer cells to gemcitabine through upregulation of ENT1 [J].
Hu, Qiangsheng ;
Qin, Yi ;
Zhang, Bo ;
Liang, Chen ;
Ji, Shunrong ;
Shi, Si ;
Xu, Wenyan ;
Xiang, Jinfeng ;
Liang, Dingkong ;
Ni, Quanxing ;
Yu, Xianjun ;
Xu, Jin .
ONCOLOGY REPORTS, 2017, 38 (04) :2069-2077
[9]   Current trends in gene recovery mediated by the CRISPR-Cas system [J].
Jang, Hyeon-Ki ;
Song, Beomjong ;
Hwang, Gue-Ho ;
Bae, Sangsu .
EXPERIMENTAL AND MOLECULAR MEDICINE, 2020, 52 (07) :1016-1027
[10]  
Kapoor A, 2014, CELL, V158, P185, DOI [10.1016/j.cell.2014.06.003, 10.1016/j.cell.2019.10.037]