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用于靶向治疗卵巢癌的可计算结构化适体

Computable structured aptamer for targeted treatment of ovarian cancer.

作者信息

Ruan Luoshan, Han Liting, Li Xin, Chen Xin, Sun Gege, Wang Xinyu, Luo Yan, Gu Chuanqi, Shi Xiaolong

机构信息

Department 2 of Gynecology, Remin Hospital of Wuhan University, Wuhan, China.

Institute of Computing Science and Technology, Guangzhou University, Guangzhou, China.

出版信息

Front Genet. 2023 May 3;14:1170260. doi: 10.3389/fgene.2023.1170260. eCollection 2023.

Abstract

Nucleolin protein expression is higher on the ovarian cancer cell surface. AS1411, a DNA aptamer, can bind with nucleolin protein specifically. In this study, we developed HA and ST DNA tiles to assemble six AS1411 aptamers to deliver doxorubicin. In addition, to superior serum stability and drug loading, HA-6AS and ST-6AS outperformed TDN-AS in cellular uptake. HA-6AS and ST-6AS exhibited satisfactory targeted cytotoxicity and achieved resounding lysosomal escape. Moreover, when injected into nude mice subcutaneous xenograft models, HA-6AS reached the peak in tumor more quickly than ST-6AS, and better expressed the active targeting ability of AS1411. Our study suggests that designing appropriate DNA tiles to assemble different aptamers to deliver different chemotherapeutic drugs is a promising treatment for ovarian cancer.

摘要

核仁素蛋白在卵巢癌细胞表面的表达较高。AS1411是一种DNA适配体,可特异性结合核仁素蛋白。在本研究中,我们开发了HA和ST DNA瓦片来组装六个AS1411适配体以递送阿霉素。此外,为了具有卓越的血清稳定性和药物负载量,HA-6AS和ST-6AS在细胞摄取方面优于TDN-AS。HA-6AS和ST-6AS表现出令人满意的靶向细胞毒性并实现了显著的溶酶体逃逸。此外,当注射到裸鼠皮下异种移植模型中时,HA-6AS比ST-6AS更快达到肿瘤峰值,并且更好地表达了AS1411的主动靶向能力。我们的研究表明,设计合适的DNA瓦片来组装不同的适配体以递送不同的化疗药物是一种有前景的卵巢癌治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af44/10189780/80d7d68ee517/fgene-14-1170260-g001.jpg

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