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FOXO1/3:潜在的纤维化抑制剂。

FOXO1/3: Potential suppressors of fibrosis.

机构信息

Key Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education, Faculty of Life Sciences, Northwest University, 229 Taibai North Road, Xi'an 710069, China; Department of Occupational and Environmental Health and The Ministry of Education Key Lab of Hazard Assessment and Control in Special Operational Environment, School of Public Health, Fourth Military Medical University, 169 Changle West Road, Xi'an 710032, China.

Department of Thoracic Surgery, Tangdu Hospital, The Fourth Military Medical University, 1 Xinsi Road, Xi'an 710038, China.

出版信息

Ageing Res Rev. 2018 Jan;41:42-52. doi: 10.1016/j.arr.2017.11.002. Epub 2017 Nov 11.

Abstract

Fibrosis is a universally age-related disease that involves nearly all organs. It is typically initiated by organic injury and eventually results in organ failure. There are still few effective therapeutic strategy targets for fibrogenesis. Forkhead box proteins O1 and O3 (FOXO1/3) have been shown to have favorable inhibitory effects on fibroblast activation and subsequent extracellular matrix production and can ameliorate fibrosis levels in numerous organs, including the heart, liver, lung, and kidney; they are therefore promising targets for anti-fibrosis therapy. Moreover, we can develop appropriate strategies to make the best use of FOXO1/3's anti-fibrosis properties. The information reviewed here should be significant for understanding the roles of FOXO1/3 in fibrosis and should contribute to the design of further studies related to FOXO1/3 and the fibrotic response and shed light on a potential treatment for fibrosis.

摘要

纤维化是一种普遍的与年龄相关的疾病,几乎涉及所有器官。它通常由有机损伤引发,最终导致器官衰竭。目前针对纤维生成,仍然很少有有效的治疗策略靶点。叉头框蛋白 O1 和 O3(FOXO1/3)已被证明对成纤维细胞的激活及随后的细胞外基质产生具有有利的抑制作用,并能改善包括心脏、肝脏、肺和肾脏在内的许多器官的纤维化水平;因此,它们是抗纤维化治疗的有希望的靶点。此外,我们可以制定适当的策略来充分利用 FOXO1/3 的抗纤维化特性。这里综述的信息对于理解 FOXO1/3 在纤维化中的作用应该具有重要意义,并有助于设计与 FOXO1/3 和纤维化反应相关的进一步研究,为纤维化的潜在治疗提供思路。

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