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儿科蒽环类药物诱导的心脏毒性:机制、药物基因组学和多能干细胞建模。

Pediatric Anthracycline-Induced Cardiotoxicity: Mechanisms, Pharmacogenomics, and Pluripotent Stem-Cell Modeling.

机构信息

Murdoch Childrens Research Institute, The Royal Children's Hospital, Parkville, Victoria, Australia.

Department of Paediatrics, The Royal Children's Hospital, The University of Melbourne, Parkville, Victoria, Australia.

出版信息

Clin Pharmacol Ther. 2019 Mar;105(3):614-624. doi: 10.1002/cpt.1311. Epub 2019 Jan 11.

Abstract

Anthracycline-induced cardiotoxicity (ACT) is a severe adverse drug reaction for a subset of children treated with anthracyclines as part of chemotherapy protocols. The identification of genetic markers associated with increased ACT susceptibility has clinical significance toward improving patient care and our understanding of the molecular mechanisms involved in ACT. Human-induced pluripotent stem cell-derived cardiomyocytes represent a novel approach to determine the pharmacogenomics of ACT and guide the development of genetic screening tests.

摘要

蒽环类药物诱导的心脏毒性(ACT)是接受蒽环类药物化疗方案治疗的一部分儿童的一种严重药物不良反应。确定与增加 ACT 易感性相关的遗传标志物对于改善患者护理和我们对 ACT 相关分子机制的理解具有临床意义。人诱导多能干细胞衍生的心肌细胞代表了一种确定 ACT 的药物基因组学并指导遗传筛选测试开发的新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbdd/6590110/7d583021ea8f/CPT-105-614-g001.jpg

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