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非病毒载体介导的体内基因递送用于癌症治疗

In vivo gene delivery mediated by non-viral vectors for cancer therapy.

作者信息

Mohammadinejad Reza, Dehshahri Ali, Sagar Madamsetty Vijay, Zahmatkeshan Masoumeh, Tavakol Shima, Makvandi Pooyan, Khorsandi Danial, Pardakhty Abbas, Ashrafizadeh Milad, Ghasemipour Afshar Elham, Zarrabi Ali

机构信息

Pharmaceutics Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences, Kerman, Iran.

Center for Nanotechnology in Drug Delivery, Shiraz University of Medical Sciences, Shiraz, Iran.

出版信息

J Control Release. 2020 Sep 10;325:249-275. doi: 10.1016/j.jconrel.2020.06.038. Epub 2020 Jul 4.

Abstract

Gene therapy by expression constructs or down-regulation of certain genes has shown great potential for the treatment of various diseases. The wide clinical application of nucleic acid materials dependents on the development of biocompatible gene carriers. There are enormous various compounds widely investigated to be used as non-viral gene carriers including lipids, polymers, carbon materials, and inorganic structures. In this review, we will discuss the recent discoveries on non-viral gene delivery systems. We will also highlight the in vivo gene delivery mediated by non-viral vectors to treat cancer in different tissue and organs including brain, breast, lung, liver, stomach, and prostate. Finally, we will delineate the state-of-the-art and promising perspective of in vivo gene editing using non-viral nano-vectors.

摘要

通过表达构建体或下调某些基因进行基因治疗已显示出治疗各种疾病的巨大潜力。核酸材料的广泛临床应用取决于生物相容性基因载体的发展。有大量不同的化合物被广泛研究用作非病毒基因载体,包括脂质、聚合物、碳材料和无机结构。在本综述中,我们将讨论非病毒基因递送系统的最新发现。我们还将强调非病毒载体介导的体内基因递送在治疗包括脑、乳腺、肺、肝、胃和前列腺在内的不同组织和器官中的癌症方面的应用。最后,我们将描述使用非病毒纳米载体进行体内基因编辑的最新进展和前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5ab/7334939/3fb12d690212/ga1_lrg.jpg

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