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SOX 因子的直接重编程:细胞命运的主宰。

Direct reprogramming with SOX factors: masters of cell fate.

机构信息

Sprott Centre for Stem Cell Research, Ottawa Hospital Research Institute, 501 Smyth Road, Ottawa, Ontario K1L8L6, Canada.

Program in Developmental and Stem Cell Biology, Hospital for Sick Children Research Institute, 686 Bay Street, Toronto, Ontario M5G0A4, Canada; Institute of Biomaterials and Biomedical Engineering, University of Toronto, 164 College Street, Toronto, Ontario M5S3G9, Canada.

出版信息

Curr Opin Genet Dev. 2017 Oct;46:24-36. doi: 10.1016/j.gde.2017.06.005. Epub 2017 Jul 4.

Abstract

Over the last decade significant advances have been made toward reprogramming the fate of somatic cells, typically by overexpression of cell lineage-determinant transcription factors. As key regulators of cell fate, the SOX family of transcription factors has emerged as potent drivers of direct somatic cell reprogramming into multiple lineages, in some cases as the sole overexpressed factor. The vast capacity of SOX factors, especially those of the SOXB1, E and F subclasses, to reprogram cell fate is enlightening our understanding of organismal development, cancer and disease, and offers tremendous potential for regenerative medicine and cell-based therapies. Understanding the molecular mechanisms through which SOX factors reprogram cell fate is essential to optimize the development of novel somatic cell transdifferentiation strategies.

摘要

在过去的十年中,人们在重编程体细胞命运方面取得了重大进展,通常是通过过度表达细胞谱系决定转录因子来实现的。作为细胞命运的关键调节因子,SOX 转录因子家族已成为将体细胞直接重编程为多种谱系的有效驱动因子,在某些情况下,它是唯一过表达的因子。SOX 因子(尤其是 SOXB1、E 和 F 亚类)的巨大重编程细胞命运的能力,使我们深入了解了机体发育、癌症和疾病,为再生医学和基于细胞的治疗提供了巨大的潜力。了解 SOX 因子重编程细胞命运的分子机制对于优化新型体细胞转分化策略的发展至关重要。

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