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血管组织工程和缺血后新生血管形成中的微小RNA

MicroRNAs in vascular tissue engineering and post-ischemic neovascularization.

作者信息

Caputo Massimo, Saif Jaimy, Rajakaruna Cha, Brooks Marcus, Angelini Gianni D, Emanueli Costanza

机构信息

Bristol Heart Institute, School of Clinical Sciences, University of Bristol, Bristol, UK; RUSH University Medical Center, Chicago, IL, USA.

Bristol Heart Institute, School of Clinical Sciences, University of Bristol, Bristol, UK.

出版信息

Adv Drug Deliv Rev. 2015 Jul 1;88:78-91. doi: 10.1016/j.addr.2015.05.003. Epub 2015 May 14.

Abstract

Increasing numbers of paediatric patients with congenital heart defects are surviving to adulthood, albeit with continuing clinical needs. Hence, there is still scope for revolutionary new strategies to correct vascular anatomical defects. Adult patients are also surviving longer with the adverse consequences of ischemic vascular disease, especially after acute coronary syndromes brought on by plaque erosion and rupture. Vascular tissue engineering and therapeutic angiogenesis provide new hope for these patients. Both approaches have shown promise in laboratory studies, but have not yet been able to deliver clear evidence of clinical success. More research into biomaterials, molecular medicine and cell and molecular therapies is necessary. This review article focuses on the new opportunities offered by targeting microRNAs for the improved production and greater empowerment of vascular cells for use in vascular tissue engineering or for increasing blood perfusion of ischemic tissues by amplifying the resident microvascular network.

摘要

越来越多患有先天性心脏缺陷的儿科患者存活至成年,尽管仍有持续的临床需求。因此,纠正血管解剖缺陷的革命性新策略仍有发展空间。成年患者也因缺血性血管疾病的不良后果而存活更长时间,尤其是在由斑块侵蚀和破裂引发的急性冠状动脉综合征之后。血管组织工程和治疗性血管生成给这些患者带来了新希望。这两种方法在实验室研究中都显示出了前景,但尚未能提供临床成功的确切证据。有必要对生物材料、分子医学以及细胞和分子疗法进行更多研究。这篇综述文章聚焦于通过靶向微小RNA来提供新机遇,以改善血管细胞的生成并增强其功能,用于血管组织工程,或通过扩增局部微血管网络来增加缺血组织的血液灌注。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5fd/4728183/ec65b36aad34/fx1.jpg

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