Suppr超能文献

通过金诺芬利用高危儿科急性淋巴细胞白血病中的活性氧物种失衡。

Exploiting the reactive oxygen species imbalance in high-risk paediatric acute lymphoblastic leukaemia through auranofin.

机构信息

Children's Cancer Institute, Lowy Cancer Research Centre, UNSW Sydney, Sydney, NSW, Australia.

School of Women's and Children's Health, UNSW Sydney, Sydney, NSW, Australia.

出版信息

Br J Cancer. 2021 Jul;125(1):55-64. doi: 10.1038/s41416-021-01332-x. Epub 2021 Apr 9.

Abstract

BACKGROUND

The prognosis for high-risk childhood acute leukaemias remains dismal and established treatment protocols often cause long-term side effects in survivors. This study aims to identify more effective and safer therapeutics for these patients.

METHODS

A high-throughput phenotypic screen of a library of 3707 approved drugs and pharmacologically active compounds was performed to identify compounds with selective cytotoxicity against leukaemia cells followed by further preclinical evaluation in patient-derived xenograft models.

RESULTS

Auranofin, an FDA-approved agent for the treatment of rheumatoid arthritis, was identified as exerting selective anti-cancer activity against leukaemia cells, including patient-derived xenograft cells from children with high-risk ALL, versus solid tumour and non-cancerous cells. It induced apoptosis in leukaemia cells by increasing reactive oxygen species (ROS) and potentiated the activity of the chemotherapeutic cytarabine against highly aggressive models of infant MLL-rearranged ALL by enhancing DNA damage accumulation. The enhanced sensitivity of leukaemia cells towards auranofin was associated with lower basal levels of the antioxidant glutathione and higher baseline ROS levels compared to solid tumour cells.

CONCLUSIONS

Our study highlights auranofin as a well-tolerated drug candidate for high-risk paediatric leukaemias that warrants further preclinical investigation for application in high-risk paediatric and adult acute leukaemias.

摘要

背景

高危儿童急性白血病的预后仍然不容乐观,既定的治疗方案往往会给幸存者带来长期的副作用。本研究旨在为这些患者寻找更有效、更安全的治疗方法。

方法

对 3707 种已批准药物和具有药理活性的化合物库进行高通量表型筛选,以鉴定对白血病细胞具有选择性细胞毒性的化合物,然后在患者来源的异种移植模型中进行进一步的临床前评估。

结果

金诺芬,一种被 FDA 批准用于治疗类风湿关节炎的药物,被鉴定为对白血病细胞具有选择性抗癌活性,包括来自高危 ALL 儿童的患者来源异种移植细胞,而对实体瘤和非癌细胞没有活性。它通过增加活性氧物种 (ROS) 诱导白血病细胞凋亡,并通过增强 DNA 损伤积累来增强阿糖胞苷对婴儿 MLL 重排 ALL 高度侵袭性模型的化疗活性。与实体瘤细胞相比,白血病细胞对金诺芬的敏感性增加与较低的基础抗氧化谷胱甘肽水平和较高的基线 ROS 水平有关。

结论

我们的研究强调了金诺芬作为一种耐受性良好的药物候选物,可用于高危儿科白血病,值得进一步进行临床前研究,以应用于高危儿科和成人急性白血病。

相似文献

5
Comparative oncology approach to drug repurposing in osteosarcoma.比较肿瘤学方法在骨肉瘤中的药物再利用。
PLoS One. 2018 Mar 26;13(3):e0194224. doi: 10.1371/journal.pone.0194224. eCollection 2018.

引用本文的文献

本文引用的文献

4

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验