摘要
背景:转移性乳腺癌的脑癌患者死亡率高。损伤的治疗在很大程度上受到血脑屏障(BBB)的阻碍,这阻止了抗癌化合物对脑转移的适当分布。 方法:在本研究中,我们使用了一种新的筛选方法来鉴定非常适合利用BBB胆碱转运蛋白分布到脑实质中的候选分子。 结果:从我们的屏幕,我们确定了两种化合物Ch-1和Ch-2能够减少乳腺癌脑转移鼠鼠模型中的脑肿瘤负荷。这些化合物也显着增加小鼠的存活超过10天。机制研究表明,Ch-1能够通过骨质疏松症(OA;糖蛋白非转移性黑素瘤蛋白B GPNMB)阻止促生存丝裂原活化激酶(MAPKs)的活化。 结论:本研究的结果表明,营养转运体虚拟筛选是一种可行的新型替代传统药物筛选程序,用于鉴定治疗脑癌的抗癌化合物。
关键词: 耐药性,CNS,分布,脑癌,药物发现,化疗,ADME。
图形摘要
Current Cancer Drug Targets
Title:Identification of Novel Agents for the Treatment of Brain Metastases of Breast Cancer
Volume: 17 Issue: 5
关键词: 耐药性,CNS,分布,脑癌,药物发现,化疗,ADME。
摘要: Background: Brain cancer from metastasized breast cancer has a high mortality rate in women. The treatment of lesions is hampered in large part by the blood-brain barrier (BBB), which prevents adequate distribution of anti-cancer compounds to brain metastases.
Method: In this study we used a novel screening method to identify candidate molecules that are well-suited to utilizing the BBB choline transporter for distribution into the brain parenchyma. Results: From our screen we identified two compounds, Ch-1 and Ch-2 that were able to reduce the brain tumor burden in a murine mouse model of brain metastasis of breast cancer. These compounds also significantly increased the survival of mice by more than 10 days. Mechanistic studies indicated that Ch-1 is able to prevent the activation of the pro-survival mitogen-activated kinases (MAPKs) by osteoactivin (OA; Glycoprotein nonmetastatic melanoma protein B GPNMB). Conclusion: The results from this study show that nutrient transporter virtual screening is a viable novel alternative to traditional drug screening programs to identify anti-cancer compounds for the treatment of brain cancers.Export Options
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Cite this article as:
Identification of Novel Agents for the Treatment of Brain Metastases of Breast Cancer, Current Cancer Drug Targets 2017; 17 (5) . https://dx.doi.org/10.2174/1568009617666161121123948
DOI https://dx.doi.org/10.2174/1568009617666161121123948 |
Print ISSN 1568-0096 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-5576 |
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