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衰老改变舒尼替尼诱导的心脏毒性严重程度:探究丝裂原活化蛋白激酶激酶7信号通路的关联

Ageing alters the severity of Sunitinib-induced cardiotoxicity: Investigating the mitogen activated kinase kinase 7 pathway association.

作者信息

Cooper Samantha, Sandhu Hardip, Hussain Afthab, Mee Christopher, Maddock Helen

机构信息

Centre for Sport, Exercise and Life Sciences, Alison Gingell Building, Faculty of Health and Life Sciences, Coventry University, CV1 2DS, United Kingdom.

出版信息

Toxicology. 2019 Jan 1;411:49-59. doi: 10.1016/j.tox.2018.10.016. Epub 2018 Oct 26.

Abstract

Anti-cancer drug Sunitinib is linked to adverse cardiovascular events, which have shown to involve mitogen activated kinase kinase 7 (MKK7) pathway. Sunitinib-induced cardiotoxicity in 3, 12 and 24 months old male Sprague-Dawley rats and MKK7 expression and activation was investigated using the Langendorff perfused heart model followed by Western blot analysis. Cardiac function and infarct size were measured during/after 125 min of Sunitinib treatment. Left ventricular cardiac samples were analysed by qRT-PCR for expression of MKK7 mRNA and cardiac injury associated microRNAs. Infarct size was increased in all Sunitinib treated age groups. Haemodynamic alterations were observed following Sunitinib administration. Left ventricular developed pressure (LVDP) was decreased in all age groups, while heart rate (HR) was decreased in 3 and 12 months groups. Sunitinib treatment decreased the expression of miR-27a in all age groups, while miR-133a and miR-133b levels were increased in 3 months and decreased in 24 months groups. MKK7 mRNA and p-MKK7 levels were decreased in the 3 months group after Sunitinib treatment. MKK7 mRNA level was increased in 24 months group and p-MKK7 levels were increased in 12 months group following Sunitinib treatment. This study highlights the importance and impact of ageing and anti-cancer therapy-induced cardiotoxicity.

摘要

抗癌药物舒尼替尼与不良心血管事件有关,这些事件已被证明涉及丝裂原活化激酶激酶7(MKK7)通路。使用Langendorff灌注心脏模型,随后进行蛋白质印迹分析,研究了舒尼替尼在3、12和24月龄雄性Sprague-Dawley大鼠中诱导的心脏毒性以及MKK7的表达和激活情况。在舒尼替尼治疗125分钟期间/之后测量心脏功能和梗死面积。通过qRT-PCR分析左心室心脏样本中MKK7 mRNA和与心脏损伤相关的微小RNA的表达。所有接受舒尼替尼治疗的年龄组梗死面积均增加。舒尼替尼给药后观察到血流动力学改变。所有年龄组的左心室舒张末压(LVDP)均降低,而3个月和12个月组的心率(HR)降低。舒尼替尼治疗使所有年龄组的miR-27a表达降低,而3个月组的miR-133a和miR-133b水平升高,24个月组降低。舒尼替尼治疗后,3个月组的MKK7 mRNA和p-MKK7水平降低。舒尼替尼治疗后,24个月组的MKK7 mRNA水平升高,12个月组的p-MKK7水平升高。这项研究突出了衰老和抗癌治疗诱导的心脏毒性的重要性和影响。

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