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在斑马鱼模型中比较雷莫芦单抗、阿帕替尼、瑞戈非尼和卡博替尼的抗血管生成和抗癌疗效的系统比较。

A systematical comparison of anti-angiogenesis and anti-cancer efficacy of ramucirumab, apatinib, regorafenib and cabozantinib in zebrafish model.

机构信息

College of Biotechnology and Pharmaceutical Engineering, Nanjing Tech University, Nanjing 211816, China.

Department of General Surgery, Jiangsu Province Hospital of Chinese Medicine, Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing 210029, China.

出版信息

Life Sci. 2020 Apr 15;247:117402. doi: 10.1016/j.lfs.2020.117402. Epub 2020 Feb 7.

Abstract

AIMS

Gastric cancer (GC) is one of the most common malignant tumors in the world. Anti-angiogenic therapy is a useful strategy for the treatment of advanced GC. This study was aimed to systemically compare the anti-angiogenesis, anti-cancer efficacy, as well as the safety of four known anti-angiogenic drugs, namely ramucirumab, apatinib, regorafenib and cabozantinib.

MAIN METHODS

Anti-angiogenic effect was evaluated for the intersegmental vessels (ISVs) and subintestinal veins (SIVs) formation in the Tg (fli-1: EGFP) zebrafish embryos. Anti-cancer efficacy was tested for the in vivo cell proliferation in cell line derived tumor xenograft (CDX) model based on Tg (fli-1: EGFP) zebrafish embryos.

KEY FINDINGS

All four drugs exhibited anti-angiogenic abilities and tumor inhibition effects in fli-1: EGFP transgenic zebrafish. Using zebrafish xenografted model, we found that effectiveness of ramucirumab in anti-GC-proliferation is better than apatinib, regorafenib and cabozantinib. The combination of anti-angiogenic drugs and cisplatin showed no significant benefit in tumors. Meanwhile, toxicity assay showed that all tested anti-angiogenic drugs could cause cardiovascular-related side effects. The therapeutic index (LD/ED) of cabozantinib is higher than apatinib and regorafenib, suggesting a potential as an anti-GC drug.

SIGNIFICANCE

The comparison of GC-related anti-angiogenic drugs was first reported. It was found that cabozantinib had a potential as an anti-GC drug. Zebrafish model was an ideal animal model for the research of anti-angiogenic behaviors.

摘要

目的

胃癌(GC)是世界上最常见的恶性肿瘤之一。抗血管生成治疗是治疗晚期 GC 的一种有效策略。本研究旨在系统比较四种已知的抗血管生成药物,即雷莫芦单抗、阿帕替尼、瑞戈非尼和卡博替尼的抗血管生成、抗癌疗效以及安全性。

主要方法

在 Tg(fli-1: EGFP)斑马鱼胚胎中评估节间血管(ISVs)和肠下静脉(SIV)形成的抗血管生成作用。基于 Tg(fli-1: EGFP)斑马鱼胚胎的细胞系衍生肿瘤异种移植(CDX)模型,测试抗癌疗效。

主要发现

四种药物均在 fli-1:EGFP 转基因斑马鱼中表现出抗血管生成能力和肿瘤抑制作用。使用斑马鱼异种移植模型,我们发现雷莫芦单抗在抗 GC 增殖方面的效果优于阿帕替尼、瑞戈非尼和卡博替尼。抗血管生成药物与顺铂联合使用对肿瘤没有明显益处。同时,毒性试验表明,所有测试的抗血管生成药物都可能引起心血管相关的副作用。卡博替尼的治疗指数(LD/ED)高于阿帕替尼和瑞戈非尼,表明其可能是一种治疗 GC 的药物。

意义

首次报道了 GC 相关抗血管生成药物的比较。发现卡博替尼可能是一种治疗 GC 的潜在药物。斑马鱼模型是研究抗血管生成行为的理想动物模型。

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