肿瘤微环境
血管生成
背景(考古学)
催眠药
癌症
癌症研究
新生血管
血管内皮生长因子
医学
血管内皮生长因子受体
肿瘤细胞
内科学
生物
古生物学
作者
Jihoon Ko,Sujin Hyung,You Jeong Heo,Sangmin Jung,Seung Tae Kim,Se Hoon Park,Jung Yong Hong,Sung Hee Lim,Kyoung‐Mee Kim,Sanghee Yoo,Noo Li Jeon,Jeeyun Lee
出处
期刊:Biomaterials
[Elsevier]
日期:2024-02-12
卷期号:306: 122504-122504
被引量:5
标识
DOI:10.1016/j.biomaterials.2024.122504
摘要
This study addresses the demand for research models that can support patient-treatment decisions and clarify the complexities of a tumor microenvironment by developing an advanced non-animal preclinical cancer model. Based on patient-derived tumor spheroids (PDTS), the proposed model reconstructs the tumor microenvironment with emphasis on tumor spheroid-driven angiogenesis. The resulting microfluidic chip system mirrors angiogenic responses elicited by PDTS, recapitulating patient-specific tumor conditions and providing robust, easily quantifiable outcomes. Vascularized PDTS exhibited marked angiogenesis and tumor proliferation on the microfluidic chip. Furthermore, a drug that targets the vascular endothelial growth factor receptor 2 (VEGFR2, ramucirumab) was deployed, which effectively inhibited angiogenesis and impeded tumor invasion. This innovative preclinical model was used for investigating distinct responses for various drug combinations, encompassing HER2 inhibitors and angiogenesis inhibitors, within the context of PDTS. This integrated platform could potentially advance precision medicine by harmonizing diverse data points within the tumor microenvironment with a focus on the interplay between cancer and the vascular system.
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