Suppr超能文献

基因组学研究正在兑现承诺:从抗衰老到疫苗和药物基因组学。

Genomic research delivering on promises: From rejuvenation to vaccines and pharmacogenetics.

机构信息

Centre for Evidence-Based Practice, Nottingham, UK.

出版信息

J Clin Pharm Ther. 2020 Jun;45(3):585-589. doi: 10.1111/jcpt.13131. Epub 2020 Mar 18.

Abstract

WHAT IS KNOWN AND OBJECTIVE

There has been astounding progress made in the treatment of disease over recent years. This progress is particularly marked in cell therapy and in the personalization of therapy based on genetic insight, an approach known as genomic medicine. Our objective is to comment on the progress made in cell and genomic medicine against an historical backcloth of the search for rejuvenation.

COMMENT

In 1741, close to seven decades after Antoine van Leeuwenhoek first saw his microscopic animalcules, Abraham Trembley, a tutor in Leiden, reported on an organism that could regenerate itself. The strange organism was thought to hold the secret of life. If it does, we have yet to prise the secret out. However, the ensuing study of cell programming and induced stem cells has shed considerable light on cellular development and provided new insights on the rejuvenative capacity of organisms. Inventive scientists have provided a deeper understanding of cell replication and, from this, developed new medicines for an increasing range of diseases. Targeted therapies, oligonucleotide therapy, therapeutic monoclonal antibodies and pharmacogenetics are all new therapeutic areas originating from the improved insights. More will surely follow.

WHAT IS NEW AND CONCLUSION

Immortality is for the gods, but man's search for its elusive secrets, perhaps as old as man himself, will continue. Huge leaps have been made, and effective medicines have been developed from our improved insights into the mechanism of life. However, only the foolish will predict how far this new knowledge will lead us, and more particularly, at what speed new therapies will follow.

摘要

已知和目的

近年来,疾病治疗取得了惊人的进展。这一进展在细胞治疗和基于基因见解的个体化治疗(即基因组医学)方面尤为显著。我们的目的是在历史背景下评论细胞和基因组医学的进展,探讨其对衰老的研究。

评论

1741 年,在安东尼·范·列文虎克首次观察到他的微观动物之后近 70 年,莱顿的一名导师亚伯拉罕·特兰布莱报告了一种能够自我再生的生物体。这种奇特的生物体被认为蕴藏着生命的秘密。如果是这样,我们还没有揭开这个秘密。然而,随后对细胞编程和诱导干细胞的研究为细胞发育提供了相当多的启示,并为生物体的再生能力提供了新的见解。有创造力的科学家对细胞复制有了更深入的了解,并在此基础上为越来越多的疾病开发了新的药物。靶向治疗、寡核苷酸治疗、治疗性单克隆抗体和药物遗传学都是源自这一改进的见解的新治疗领域。肯定会有更多的领域出现。

新内容和结论

永生是神的领域,但是人类对其难以捉摸的秘密的追求,也许和人类本身一样古老,将继续下去。已经取得了巨大的飞跃,从我们对生命机制的认识的提高中,已经开发出了有效的药物。然而,只有愚蠢的人才会预测这些新知识将把我们带到多远,更特别是,新疗法将以多快的速度跟进。

相似文献

6
Pharmacogenetics: from description to prediction.药物遗传学:从描述到预测。
Clin Lab Med. 2008 Dec;28(4):499-511. doi: 10.1016/j.cll.2008.05.002.
9
Chapter 33: the history of movement disorders.第33章:运动障碍病史。
Handb Clin Neurol. 2010;95:501-46. doi: 10.1016/S0072-9752(08)02133-7.

本文引用的文献

3
A Novel Coronavirus from Patients with Pneumonia in China, 2019.2019 年中国肺炎患者中的一种新型冠状病毒。
N Engl J Med. 2020 Feb 20;382(8):727-733. doi: 10.1056/NEJMoa2001017. Epub 2020 Jan 24.
4
China delivers verdict on gene editing of babies.中国对基因编辑婴儿作出裁决。
Science. 2020 Jan 10;367(6474):130. doi: 10.1126/science.367.6474.130.
6
Realizing the Dream of Molecularly Targeted Therapies for Cystic Fibrosis.实现囊性纤维化分子靶向治疗的梦想。
N Engl J Med. 2019 Nov 7;381(19):1863-1865. doi: 10.1056/NEJMe1911602. Epub 2019 Oct 31.
7
Modeling the Placenta with Stem Cells.用干细胞构建胎盘模型。
N Engl J Med. 2019 Oct 24;381(17):1681-1683. doi: 10.1056/NEJMcibr1907773.
8
Clopidogrel Pharmacogenetics - Why the Wait?氯吡格雷药物遗传学——为何要等待?
N Engl J Med. 2019 Oct 24;381(17):1677-1678. doi: 10.1056/NEJMe1911496.
9
Hereditary Thrombotic Thrombocytopenic Purpura.遗传性血栓性血小板减少性紫癜
N Engl J Med. 2019 Oct 24;381(17):1653-1662. doi: 10.1056/NEJMra1813013.
10
Patient-Customized Oligonucleotide Therapy for a Rare Genetic Disease.患者定制型寡核苷酸疗法治疗罕见遗传病。
N Engl J Med. 2019 Oct 24;381(17):1644-1652. doi: 10.1056/NEJMoa1813279. Epub 2019 Oct 9.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验