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基因兴奋剂:概述及对运动员的当前影响。

Gene doping: an overview and current implications for athletes.

机构信息

Department of Pharmacoepidemiology & Clinical Pharmacology, Utrecht Institute for Pharmaceutical Sciences (UIPS), Utrecht University, Utrecht, The Netherlands.

出版信息

Br J Sports Med. 2013 Jul;47(11):670-8. doi: 10.1136/bjsports-2012-091288. Epub 2013 Jan 15.

Abstract

The possibility of gene doping, defined as the transfer of nucleic acid sequences and/or the use of normal or genetically modified cells to enhance sport performance, is a real concern in sports medicine. The abuse of knowledge and techniques gained in the area of gene therapy is a form of doping, and is prohibited for competitive athletes. As yet there is no conclusive evidence that that gene doping has been practiced in sport. However, given that gene therapy techniques improve continuously, the likelihood of abuse will increase. A literature search was conducted to identify the most relevant proteins based on their current gene doping potential using articles from Pubmed, Scopus and Embase published between 2006 and 2011. The final list of selected proteins were erythropoietin, insulin-like growth factor, growth hormone, myostatin, vascular endothelial growth factor, fibroblast growth factor, endorphin and enkephalin, α actinin 3, peroxisome proliferator-activated receptor-delta (PPARδ) and cytosolic phosphoenolpyruvate carboxykinase (PEPCK-C). We discuss these proteins with respect to their potential benefits, existing gene therapy experience in humans, potential risks, and chances of detection in current and future anti-doping controls. We have identified PPARδ and PEPCK-C as having high potential for abuse. But we expect that for efficiency reasons, there will be a preference for inserting gene target combinations rather than single gene doping products. This will also further complicate detection.

摘要

基因兴奋剂的可能性,定义为转移核酸序列和/或使用正常或基因修饰细胞来提高运动表现,是运动医学中的一个真正关注点。滥用基因治疗领域获得的知识和技术是一种兴奋剂形式,竞技运动员被禁止使用。尽管目前还没有确凿的证据表明运动中存在基因兴奋剂,但鉴于基因治疗技术不断提高,滥用的可能性将会增加。使用 2006 年至 2011 年间发表于 Pubmed、Scopus 和 Embase 的文章,进行了文献检索,以确定基于当前基因兴奋剂潜力的最相关蛋白质。选择的蛋白质最终列表包括:促红细胞生成素、胰岛素样生长因子、生长激素、肌肉生长抑制素、血管内皮生长因子、成纤维细胞生长因子、内啡肽和脑啡肽、α 辅肌动蛋白 3、过氧化物酶体增殖物激活受体-δ(PPARδ)和细胞质磷酸烯醇丙酮酸羧激酶(PEPCK-C)。我们根据这些蛋白质的潜在益处、人类现有的基因治疗经验、潜在风险以及在当前和未来反兴奋剂控制中检测的可能性,对它们进行了讨论。我们已经确定了 PPARδ 和 PEPCK-C 具有很高的滥用潜力。但我们预计,出于效率原因,插入基因靶组合而不是单一基因兴奋剂产品将成为首选。这也将使检测更加复杂。

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