Department of Hematology and Oncology, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.
Nat Commun. 2022 Nov 22;13(1):7171. doi: 10.1038/s41467-022-34917-y.
Anthracyclines, widely used to treat breast cancer, have the potential for cardiotoxicity. We have previously identified and validated a germline single nucleotide polymorphism, rs28714259, associated with an increased risk of anthracycline-induced heart failure. We now provide insights into the mechanism by which rs28714259 might confer increased risk of cardiac damage. Using hiPSC-derived cardiomyocyte cell lines with either intrinsic polymorphism or CRISPR-Cas9-mediated deletion of rs28714259 locus, we demonstrate that glucocorticoid receptor signaling activated by dexamethasone pretreatment prior to doxorubicin exposure preserves cardiomyocyte viability and contractility in cardiomyocytes containing the major allele. Homozygous loss of the rs28714259 major allele diminishes dexamethasone's protective effect. We further demonstrate that the risk allele of rs28714259 disrupts glucocorticoid receptor and rs28714259 binding affinity. Finally, we highlight the activation of genes and pathways involved in cardiac hypertrophy signaling that are blocked by the risk allele, suggesting a decreased adaptive survival response to doxorubicin-related stress.
蒽环类药物被广泛用于治疗乳腺癌,但有潜在的心脏毒性。我们之前已经鉴定并验证了一个与蒽环类药物诱导的心力衰竭风险增加相关的种系单核苷酸多态性 rs28714259。现在,我们提供了有关 rs28714259 可能增加心脏损伤风险的机制的见解。使用具有内在多态性或 CRISPR-Cas9 介导的 rs28714259 基因座缺失的 hiPSC 衍生心肌细胞系,我们证明了地塞米松预处理后再给予阿霉素暴露时,糖皮质激素受体信号激活可在含有主要等位基因的心肌细胞中保持心肌细胞活力和收缩性。rs28714259 主要等位基因的纯合缺失会降低地塞米松的保护作用。我们进一步证明 rs28714259 的风险等位基因会破坏糖皮质激素受体和 rs28714259 的结合亲和力。最后,我们强调了与心脏肥大信号转导相关的基因和途径的激活,这些基因和途径被风险等位基因阻断,表明对阿霉素相关应激的适应性存活反应降低。