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高通量筛选鉴定出两类抗生素作为辐射防护剂:四环素类和氟喹诺酮类。

High-throughput screening identifies two classes of antibiotics as radioprotectors: tetracyclines and fluoroquinolones.

机构信息

Department of Radiation Oncology, David Geffen School of Medicine at University of California at Los Angeles, Los Angeles, California 90095-1714, USA.

出版信息

Clin Cancer Res. 2009 Dec 1;15(23):7238-45. doi: 10.1158/1078-0432.CCR-09-1964. Epub 2009 Nov 17.

Abstract

PURPOSE

Discovery of agents that protect or mitigate normal tissue from radiation injury during radiotherapy, accidents, or terrorist attacks is of importance. Specifically, bone marrow insufficiency, with possible infection due to immunosuppression, can occur after total body irradiation (TBI) or regional irradiation and is a major component of the acute radiation syndrome. The purpose of this study was to identify novel radioprotectors and mitigators of the hematopoietic system.

EXPERIMENTAL DESIGN

High-throughput screening of small-molecule libraries was done using viability of a murine lymphocyte line as a readout with further validation in human lymphoblastoid cells. The selected compounds were then tested for their ability to counter TBI lethality in mice.

RESULTS

All of two major classes of antibiotics, tetracyclines and fluoroquinolones, which share a common planar ring moiety, were radioprotective. Furthermore, tetracycline protected murine hematopoietic stem/progenitor cell populations from radiation damage and allowed 87.5% of mice to survive when given before and 35% when given 24 h after lethal TBI. Interestingly, tetracycline did not alter the radiosensitivity of Lewis lung cancer cells. Tetracycline and ciprofloxacine also protected human lymphoblastoid cells, reducing radiation-induced DNA double-strand breaks by 33% and 21%, respectively. The effects of these agents on radiation lethality are not due to the classic mechanism of free radical scavenging but potentially through activation of the Tip60 histone acetyltransferase and altered chromatin structure.

CONCLUSIONS

Tetracyclines and fluoroquinolones can be robust radioprotectors and mitigators of the hematopoietic system with potential utility in anticancer radiotherapy and radiation emergencies.

摘要

目的

发现能够保护或减轻正常组织免受放疗、事故或恐怖袭击中辐射损伤的药物非常重要。具体而言,全身照射(TBI)或局部照射后可能会出现骨髓衰竭,并伴有免疫抑制引起的感染,这是急性辐射综合征的主要组成部分。本研究旨在确定新的造血系统放射保护剂和缓解剂。

实验设计

使用小鼠淋巴细胞系的活力作为读数,对小分子文库进行高通量筛选,并在人淋巴母细胞中进一步验证。然后测试所选化合物对抗小鼠 TBI 致死的能力。

结果

两类主要抗生素——四环素类和氟喹诺酮类,它们都具有共同的平面环部分,都具有放射保护作用。此外,四环素可保护小鼠造血干/祖细胞免受辐射损伤,并使 87.5%的小鼠在致死性 TBI 前给予和 35%的小鼠在 24 小时后给予时存活。有趣的是,四环素不会改变 Lewis 肺癌细胞的辐射敏感性。四环素和环丙沙星还可保护人淋巴母细胞,分别将辐射诱导的 DNA 双链断裂减少 33%和 21%。这些药物对辐射致死的作用不是由于自由基清除的经典机制,而是可能通过激活 Tip60 组蛋白乙酰转移酶和改变染色质结构。

结论

四环素类和氟喹诺酮类药物可以作为造血系统的有效放射保护剂和缓解剂,在癌症放疗和辐射紧急情况下具有潜在的应用价值。

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本文引用的文献

1
Radioprotection.辐射防护
In Vivo. 2009 Mar-Apr;23(2):323-36.
10
Immunomodulatory activities of fluoroquinolones.氟喹诺酮类药物的免疫调节活性。
Infection. 2005 Dec;33 Suppl 2:55-70. doi: 10.1007/s15010-005-8209-8.

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