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作为细胞分化调节剂的转录因子的递送。

Delivery of transcription factors as modulators of cell differentiation.

作者信息

Rilo-Alvarez Héctor, Ledo Adriana M, Vidal Anxo, Garcia-Fuentes Marcos

机构信息

Department of Pharmacology, Pharmacy and Pharmaceutical Technology, IDIS Research Institute, CiMUS Research Institute, University of Santiago de Compostela, 15782, Santiago de Compostela, Spain.

Respiratory Therapeutic Area, Novartis Institutes for BioMedical Research, Inc, 700 Main Street, Cambridge, MA, 02139, USA.

出版信息

Drug Deliv Transl Res. 2021 Apr;11(2):426-444. doi: 10.1007/s13346-021-00931-8. Epub 2021 Feb 20.

Abstract

Fundamental studies performed during the last decades have shown that cell fate is much more plastic than previously considered, and technologies for its manipulation are a keystone for many new tissue regeneration therapies. Transcription factors (TFs) are DNA-binding proteins that control gene expression, and they have critical roles in the control of cell fate and other cellular behavior. TF-based therapies have much medical potential, but their use as drugs depends on the development of suitable delivery technologies that can help them reach their action site inside of the cells. TFs can be used either as proteins or encoded in polynucleotides. When used in protein form, many TFs require to be associated to a cell-penetrating peptide or another transduction domain. As polynucleotides, they can be delivered either by viral carriers or by non-viral systems such as polyplexes and lipoplexes. TF-based therapies have extensively shown their potential to solve many tissue-engineering problems, including bone, cartilage and cardiac regeneration. Yet, their use has expanded beyond regenerative medicine to other prominent disease areas such as cancer therapy and immunomodulation. This review summarizes some of the delivery options for effective TF-based therapies and their current main applications.

摘要

过去几十年进行的基础研究表明,细胞命运比之前认为的更具可塑性,而操控细胞命运的技术是许多新型组织再生疗法的关键。转录因子(TFs)是控制基因表达的DNA结合蛋白,在控制细胞命运和其他细胞行为方面发挥着关键作用。基于转录因子的疗法具有很大的医学潜力,但其作为药物使用取决于合适递送技术的开发,这些技术能够帮助它们抵达细胞内的作用位点。转录因子既可以以蛋白质形式使用,也可以编码于多核苷酸中。以蛋白质形式使用时,许多转录因子需要与细胞穿透肽或其他转导结构域结合。作为多核苷酸,它们可以通过病毒载体或非病毒系统(如多聚体和脂质体)递送。基于转录因子的疗法已广泛展示出解决许多组织工程问题的潜力,包括骨骼、软骨和心脏再生。然而,其应用范围已从再生医学扩展到其他重要疾病领域,如癌症治疗和免疫调节。本综述总结了一些基于转录因子的有效疗法的递送选择及其当前的主要应用。

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