循环microrna作为大鼠视网膜毒性生物标志物的诊断性能评价。

IF 2.7 4区 医学 Q3 TOXICOLOGY
Daichi Ishii, Yuki Nishikawa, Miharu Soeda, Yutaka Tonomura, Yuki Numakura, Yoko Kitsunai, Yuki Osawa, Keiichi Asakura, Yasuhiro Yamashita
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引用次数: 0

摘要

由于视网膜毒性的不可逆性,在药物开发过程中备受关注。据报道,循环microRNA (miRNA)可用于检测大鼠视网膜毒性,尽管尚无统计学分析评估其诊断性能。因此,我们比较分析了在视网膜中富集的循环mirna的诊断性能,如rno-miR-124-3p、-183-5p、-96-5p、-182、-9a-5p、-125b-5p、-204-5p和-211-5p。本研究中使用的毒性物质对大鼠视网膜感光细胞(PR)、神经视网膜细胞(NR)和视网膜色素上皮细胞(RPE)造成三种类型的损伤。通过受试者操作特征(ROC)分析评估这些视网膜毒性生物标志物的性能,然后计算组织病理视网膜病变的截止值以及ROC曲线下面积(ROC- auc)、敏感性和特异性等性能指标。PR细胞毒性与rno-miR-183-5p和-182的ROC-AUC分别为0.970和0.873,NR细胞毒性与rno-miR-124-3p的ROC-AUC为0.896。我们的研究结果表明,血浆中的rno-miR-124-3p和-183-5p/-182分别适用于检测NR细胞毒性和PR细胞毒性。总之,这些血浆mirna可能是临床前毒理学研究中检测药物性视网膜毒性的有效筛选工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of Diagnostic Performance of Circulating microRNAs as Biomarkers of Retinal Toxicity in the Rat

Retinal toxicity is of great concern during drug development due to the irreversibility. Circulating microRNA (miRNA) is reported to be useful for detecting retinal toxicity in rats, although there has been no assessment of the diagnostic performance with statistical analysis. Therefore, we comparatively analyzed the diagnostic performance of circulating miRNAs enriched in the retina such as rno-miR-124-3p, -183-5p, -96-5p, -182, -9a-5p, -125b-5p, -204-5p and -211-5p. The toxicants used in this study resulted in three types of retinal injury in photoreceptor (PR) cells, neuroretinal (NR) cells and retinal pigment epithelium (RPE) cells in rats. The performance of these biomarkers of retinal toxicity were assessed by receiver operator characteristic (ROC) analysis, then cut-off values indicating the histopathological retinal lesions and performance indexes such as area under the ROC curve (ROC-AUC), sensitivity and specificity were calculated. The ROC-AUC for PR cell toxicity in relation to rno-miR-183-5p and -182 were 0.970 and 0.873, respectively, and for NR cell toxicity in relation to rno-miR-124-3p it was 0.896. Our results suggest that plasma rno-miR-124-3p and -183-5p/-182 would be suitable for detecting NR cell toxicity and PR cell toxicity, respectively. In conclusion, these plasma miRNAs may be an effective screening tool to detect drug-induced retinal toxicity in preclinical toxicology studies.

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来源期刊
CiteScore
7.00
自引率
6.10%
发文量
145
审稿时长
1 months
期刊介绍: Journal of Applied Toxicology publishes peer-reviewed original reviews and hypothesis-driven research articles on mechanistic, fundamental and applied research relating to the toxicity of drugs and chemicals at the molecular, cellular, tissue, target organ and whole body level in vivo (by all relevant routes of exposure) and in vitro / ex vivo. All aspects of toxicology are covered (including but not limited to nanotoxicology, genomics and proteomics, teratogenesis, carcinogenesis, mutagenesis, reproductive and endocrine toxicology, toxicopathology, target organ toxicity, systems toxicity (eg immunotoxicity), neurobehavioral toxicology, mechanistic studies, biochemical and molecular toxicology, novel biomarkers, pharmacokinetics/PBPK, risk assessment and environmental health studies) and emphasis is given to papers of clear application to human health, and/or advance mechanistic understanding and/or provide significant contributions and impact to their field.
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