In vivo modelling recapitulates radiotherapy delivery and late-effect profile for childhood medulloblastoma

IF 3.7 Q1 CLINICAL NEUROLOGY
Jemma Castle, Gary Shaw, Dominic Weller, E. Fielder, T. Egnuni, Mankaran Singh, Roderick Skinner, T. von Zglinicki, Steven C. Clifford, Susan C Short, Satomi Miwa, Debbie Hicks
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引用次数: 0

Abstract

Medulloblastoma (MB) is the most common malignant paediatric brain tumour, with 5-year survival rates >70%. Cranial radiotherapy (CRT) to the whole-brain, with posterior fossa boost (PFB), underpins treatment for non-infants, however, radiotherapeutic insult to normal brain has deleterious consequences to neurocognitive and physical functioning, and causes accelerated ageing/frailty. Approaches to ameliorate radiotherapy-induced late-effects are lacking and a paucity of appropriate model systems hinders their development. We have developed a clinically-relevant in vivo model system that recapitulates the radiotherapy dose, targeting and developmental stage of childhood medulloblastoma. Consistent with human regimens, age-equivalent (postnatal days 35-37) male C57Bl/6J mice received CT image-guided CRT (human-equivalent 37.5 Gy EQD2, n=12) ± PFB (human-equivalent 48.7 Gy EQD2, n=12), via the small animal radiation research platform (SARRP) and were longitudinally assessed for >12 months. CRT was well tolerated, independent of PFB receipt. Compared to a sham-irradiated group (n=12), irradiated mice were significantly frailer following irradiation (frailty index; p=0.0002) and had reduced physical functioning; time to fall from a rotating rod (rotarod; p=0.026) and grip strength (p=0.006) were significantly lower. Neurocognitive deficits were consistent with childhood MB survivors; irradiated mice displayed significantly worse working memory (Y-maze; p=0.009) and exhibited spatial memory deficits (Barnes maze; p=0.029). Receipt of PFB did not induce a more severe late-effect profile. Our in vivo model mirrored childhood MB radiotherapy and recapitulated features observed in the late-effect profile of MB survivors. Our clinically-relevant model will facilitate both the elucidation of novel/target mechanisms underpinning MB late-effects and the development of novel interventions for their amelioration.
体内建模再现儿童髓母细胞瘤的放疗给药和后期疗效特征
髓母细胞瘤(MB)是最常见的儿童恶性脑肿瘤,5年生存率超过70%。全脑颅骨放疗(CRT)和后窝增量放疗(PFB)是治疗非婴儿脑肿瘤的主要方法,然而,对正常大脑的放疗损伤会对神经认知和身体功能造成有害影响,并导致加速衰老/虚弱。目前还缺乏改善放疗诱发的晚期效应的方法,而且缺乏合适的模型系统也阻碍了这些方法的开发。 我们开发了一种与临床相关的体内模型系统,该系统再现了儿童髓母细胞瘤的放疗剂量、靶向和发育阶段。通过小动物放射研究平台(SARRP),年龄相当(出生后第35-37天)的雄性C57Bl/6J小鼠接受了CT图像引导的CRT(相当于人类的37.5 Gy EQD2,n=12)± PFB(相当于人类的48.7 Gy EQD2,n=12),并接受了12个月以上的纵向评估。 CRT的耐受性良好,与是否接受PFB无关。与假辐照组(n=12)相比,辐照后的小鼠明显更虚弱(虚弱指数;p=0.0002),身体机能下降;从旋转杆(rotarod;p=0.026)上跌落的时间和握力(p=0.006)明显降低。神经认知缺陷与儿童甲基溴幸存者一致;辐照小鼠的工作记忆(Y-迷宫;p=0.009)和空间记忆(巴恩斯迷宫;p=0.029)明显较差。接受全氟辛酸不会导致更严重的后期效应。 我们的体内模型反映了儿童甲基溴放疗的情况,并再现了在甲基溴幸存者晚期效应特征中观察到的特征。我们的临床相关模型将有助于阐明导致甲基溴晚期效应的新机制/目标机制,并开发新的干预措施来改善晚期效应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.20
自引率
0.00%
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0
审稿时长
12 weeks
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