Engineered Exosomes-Mediated Transfer of hsa-miR-320a Overcomes Chemoresistance in Cervical Cancer Cells via Targeting MCL1

被引:6
|
作者
Zhou, Jinling [1 ]
Wang, Yuanhe [1 ]
Zhang, Lizhu [2 ]
Chen, Qin [3 ]
Zhu, Xiaojun [1 ]
Jiang, Peiyue [1 ]
Jiang, Nan [4 ]
Zhao, Wei [5 ,6 ]
Li, Baohua [1 ]
机构
[1] Zhejiang Univ, Womens Hosp, Dept Obstet & Gynecol, Sch Med, Hangzhou, Peoples R China
[2] Inst Nanjing Nanxin Pharmaceut Technol Res, Nanjing, Peoples R China
[3] Zhejiang Univ, Womens Hosp, Dept Pathol, Sch Med, Hangzhou, Peoples R China
[4] Zhejiang Univ, Womens Hosp, Dept Clin Lab, Sch Med, Hangzhou, Peoples R China
[5] City Univ Hong Kong, Dept Biomed Sci, Hong Kong, Peoples R China
[6] City Univ Hong Kong, Tung Biomed Sci Ctr, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
engineered exosomes; cervical cancer; has-miR-320a; Mcl1; chemoresistance; CISPLATIN-RESISTANCE; MIR-320A;
D O I
10.3389/fphar.2022.883445
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In cervical cancer (CC), cisplatin resistance greatly restricts the application in clinical. Here, we report that engineered exosomes-mediated transfer of hsa-miR-320a overcomes chemoresistance in cervical cancer cells via targeting Myeloid Cell Leukemia Sequence 1 (MCL1). In DDP resistant CC tissues, as well as cell lines, it was found that miR-320a expression is lower, engineered miR-320a exosomes were used to attenuate DDP resistance in Hela/DDP and Caski/DDP cells. Mechanistically, we find that MCL1, which is a target of miR-320a, overcomes DDP resistance in Hela/DDP cells and in mice. In conclusion, we report that the engineered miR-320a exosomes is proved to be effective and safe.
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页数:10
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