Lee Seonhwa, Lee Hae-June, Kang Hyunji, Kim Eun-Ho, Lim Young-Cheol, Park Hyejin, Lim Sang Moo, Lee Yong Jin, Kim Jung Min, Kim Jin Su
Division of RI application, Korea Institute of Radiological and Medical Sciences, 75 Nowon-ro, Nowon-gu, Seoul 01812, Korea.
Department of Bio-convergence Engineering, Korea University, Seoul 02856, Korea.
J Clin Med. 2019 Feb 11;8(2):234. doi: 10.3390/jcm8020234.
The authors identified that chemo-brain was induced after trastuzumab (TZB) therapy. In addition, atorvastatin (ATV) could rescue chemo-brain during trastuzumab (TZB) therapy. Enhanced therapeutic effect of TZB was confirmed after ATV therapy. We also investigated that there was no hair loss side effect due to ATV therapy. In an animal model, 150 μg TZB and five serial doses of 20 mg/kg ATV were administered. F-fluorodeoxyglucose Positron Emission Tomography (PET) and Magnetic Resonance Imaging (MRI) data were acquired. Statistical parametric mapping analysis and voxel-based morphometry analysis were performed to identify differences in glucose metabolism and gray matter concentration. The enhanced therapeutic efficacy of TZB after ATV treatment was assessed using a human epidermal growth factor receptor 2-positive gastric cancer model. We found a decrease in cerebral glucose metabolism and gray matter concentration in the frontal lobe following TZB therapy ( < 0.005). After subsequent ATV administration, glucose metabolism and regional gray matter concentration were rescued ( < 0.005). Cognitive impairment due to TZB and the rescue effect of ATV were confirmed using a passive avoidance test and quantitative real-time reverse transcription PCR. Furthermore, the penetration and accumulation of TZB in tumors increased by 100% after ATV co-administration, which resulted in an enhanced anti-cancer effect. Our study collectively demonstrates that ATV co-administration with TZB rescued the TZB-induced chemo-brain and enhances the therapeutic efficacy of TZB in tumors. We also showed that there was no hair loss during ATV therapy.
作者发现曲妥珠单抗(TZB)治疗后会诱发化疗脑。此外,阿托伐他汀(ATV)可在曲妥珠单抗(TZB)治疗期间挽救化疗脑。ATV治疗后证实了TZB的治疗效果增强。我们还研究发现ATV治疗没有脱发副作用。在动物模型中,给予150μg TZB和五剂连续剂量的20mg/kg ATV。采集了F-氟脱氧葡萄糖正电子发射断层扫描(PET)和磁共振成像(MRI)数据。进行了统计参数映射分析和基于体素的形态计量分析,以确定葡萄糖代谢和灰质浓度的差异。使用人表皮生长因子受体2阳性胃癌模型评估了ATV治疗后TZB增强的治疗效果。我们发现TZB治疗后额叶的脑葡萄糖代谢和灰质浓度降低(<0.005)。随后给予ATV后,葡萄糖代谢和局部灰质浓度得到挽救(<0.005)。使用被动回避试验和定量实时逆转录PCR证实了TZB引起的认知障碍和ATV的挽救作用。此外,ATV联合给药后,TZB在肿瘤中的渗透和积累增加了100%,从而增强了抗癌效果。我们的研究共同表明,ATV与TZB联合给药可挽救TZB诱导的化疗脑,并增强TZB在肿瘤中的治疗效果。我们还表明ATV治疗期间没有脱发。