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他汀类药物与醋酸阿比特龙对靶向雄激素受体的神经母细胞瘤生长抑制的协同作用

Synergistic Effect of Statins and Abiraterone Acetate on the Growth Inhibition of Neuroblastoma Targeting Androgen Receptor.

作者信息

Hu Zengchun, Cheng Chuandong, Wang Yue, Chen Tianrui, Tu Junhong, Niu Chaoshi, Xing Rong, Wang Yang, Xu Yinghui

机构信息

Dalian Medical University, Dalian, China.

Department of Neurosurgery, 2nd Affiliated Hospital of Dalian Medical University, Dalian, China.

出版信息

Front Oncol. 2021 May 10;11:595285. doi: 10.3389/fonc.2021.595285. eCollection 2021.

Abstract

Neuroblastoma is the most common extracranial neuroendocrine tumor in childhood. Although many studies have tried to find effective treatments, there are still numerous limitations in current clinical targeted therapy. So, it is important to find new therapeutic targets and strategies from a new perspective. Our previous study reported that the androgen receptor (AR) promotes the growth of neuroblastoma and . Based on documentary investigation, we postulated that the AR-SCAP-SREBPs-CYP17/HMGCR axis may regulate cholesterol and androgens synthesis and form a positive enhancement loop promoting NB progression. Clinical samples and Oncomine database analysis proved the activation of AR-SCAP-SREBPs-CYP17/HMGCR axis in neuroblastoma. The combination of inhibitors of HMGCR (statins) and CYP17A1 (abiraterone acetate) showed synergistic effect that significantly inhibited the proliferation and migration with decreased expression of related genes detected and suggesting the dual-targeted therapy had the potential to inhibit the progression of neuroblastoma in spite of its MYCN status. This study provides new ideas for clinical treatment of neuroblastoma with efficacy and reduced toxicity.

摘要

神经母细胞瘤是儿童时期最常见的颅外神经内分泌肿瘤。尽管许多研究试图找到有效的治疗方法,但目前临床靶向治疗仍存在诸多局限性。因此,从新的角度寻找新的治疗靶点和策略很重要。我们之前的研究报道雄激素受体(AR)促进神经母细胞瘤的生长。基于文献调查,我们推测AR-SCAP-SREBPs-CYP17/HMGCR轴可能调节胆固醇和雄激素的合成,并形成促进神经母细胞瘤进展的正反馈增强环路。临床样本和Oncomine数据库分析证实了神经母细胞瘤中AR-SCAP-SREBPs-CYP17/HMGCR轴的激活。HMGCR抑制剂(他汀类药物)和CYP17A1抑制剂(醋酸阿比特龙)联合使用显示出协同效应,显著抑制了增殖和迁移,相关基因表达降低,这表明双靶点治疗尽管与MYCN状态无关,但仍有可能抑制神经母细胞瘤的进展。本研究为神经母细胞瘤的临床治疗提供了疗效好且毒性低的新思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11f5/8141582/79d7a23a3ba4/fonc-11-595285-g001.jpg

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