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Modeling pegylated liposomal doxorubicin-induced hand-foot syndrome and intestinal mucositis in zebrafish

机译:模拟斑马鱼中的聚乙二醇化脂质体阿霉素诱导的手足综合征和肠粘膜炎

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摘要

Pegylated liposomal doxorubicin (PLD) has been widely used to treat cancer. The adverse effects of PLD noted in clinical practice, especially hand-foot syndrome (HFS), are regarded as unique, and the management methods for them remain limited. This study was aimed at developing a feasible experimental model for translational medicine to solve this clinical issue by using skin fluorescent transgenic zebrafish. We established an optimal protocol for the administration of Lipo-Dox™, a PLD in current clinical use, to the Tg(k18:dsred) zebrafish line expressing red fluorescence in keratinocytes. We made use of bodyweight, survival rate, gross observation, flssuorescent microscopic assessment, and pathological examination of the zebrafish to assess this model. The consecutive administration protocol of PLD resulted in growth retardation of the zebrafish embryo and survival impairment, indicating establishment of a significant toxicity. We observed fin necrosis and keratinocyte dissociation phenotypes in the PLD-treated fish after consecutive administration. The skin toxicity induced by the Lipo-Dox injection was subsequently reversible, which might be compatible with a clinical course of skin recovery after discontinuation of Lipo-Dox administration. Furthermore, we found that the number of intestinal goblet cells, an important marker of intestinal inflammation, in the Lipo-Dox-injected zebrafish was markedly increased, accompanied by impaired mucosal integrity. The intestinal inflammation induced by Lipo-Dox resembled the intestinal mucositis the clinical patients suffered from after the administration of PLD. In conclusion, we established a zebrafish model for PLD-induced HFS. The intestinal mucositis simultaneously noted in the PLD-treated zebrafish validated the similarity of clinical courses after administration of PLD. This model is easily assessable, efficient, and worthy for use in developing a new therapeutic protocol for prevention or treatment of HFS as well as intestinal mucositis. Further clinical investigations to validate the correlation between human and zebrafish data are warranted.
机译:聚乙二醇化脂质体阿霉素(PLD)已被广泛用于治疗癌症。在临床实践中注意到的PLD的不利影响,尤其是手足综合征(HFS),被认为是独特的,并且对其的管理方法仍然有限。这项研究旨在开发一种可行的转化医学实验模型,以通过使用皮肤荧光转基因斑马鱼解决这一临床问题。我们建立了将Lipo-Dox™(一种目前临床使用的PLD)给药于在角质形成细胞中表达红色荧光的Tg(k18:dsred)斑马鱼品系的最佳方案。我们利用体重,存活率,总体观察,萤光显微镜评估和斑马鱼的病理检查来评估该模型。 PLD的连续给药方案导致斑马鱼胚胎的生长发育迟缓和生存受损,表明建立了明显的毒性。在连续给药后,我们在PLD处理的鱼中观察到鳍坏死和角质形成细胞解离表型。随后,由Lipo-Dox注射引起的皮肤毒性是可逆的,这可能与中断Lipo-Dox给药后皮肤恢复的临床过程兼容。此外,我们发现在注射了Lipo-Dox的斑马鱼中,肠道杯状细胞(肠道炎症的重要标志)的数量显着增加,并伴有粘膜完整性受损。由Lipo-Dox引起的肠道炎症类似于临床患者服用PLD后所遭受的肠道粘膜炎。总之,我们为PLD诱导的HFS建立了斑马鱼模型。在PLD治疗的斑马鱼中同时注意到的肠粘膜炎证实了PLD给药后临床过程的相似性。该模型易于评估,有效并且值得用于开发预防或治疗HFS以及肠粘膜炎的新治疗方案。有必要进行进一步的临床研究以验证人与斑马鱼数据之间的相关性。

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