Channel-assembling tumor microenvironment on-chip for evaluating anticancer drug efficacy

被引:0
|
作者
Lee, Jaehun [1 ,2 ]
Kim, Youngwon [1 ,2 ]
Jung, Hyo-Il [1 ,5 ]
Lim, Jiseok [3 ,4 ]
Kwak, Bong Seop [2 ,3 ]
机构
[1] Yonsei Univ, Sch Mech Engn, 50 Yonsei Ro, Seoul 03722, South Korea
[2] Dongguk Univ, Coll Med, 32 Dongguk Ro, Goyangsi 10326, Gyeonggi Do, South Korea
[3] MediSphere Inc, Gyongsan, Gyeongsanbuk Do, South Korea
[4] Yeungnam Univ, Sch Mech Engn, 280 Daehak Ro, Gyongsan 38541, Gyeongsangbuk D, South Korea
[5] DABOM Inc, 50 Yonsei Ro, Seoul 03722, South Korea
基金
新加坡国家研究基金会;
关键词
Organ-on-a-chip; Tumor microenvironment-on-chip; Channel-assembling tumor microenvironmenton-chip (CATOC); Chemical and targeted anticancer drug; Precision medicine; CANCER; TRASTUZUMAB; DOXORUBICIN; RESISTANCE;
D O I
10.1016/j.jconrel.2024.11.030
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Organ-on-a-chip is an advanced system for evaluating drug response in diseases. It simulates the in vivo tumor microenvironment, aiding in the understanding of drug mechanisms and tumor responses. It mimics the structure of the tumor microenvironment and the dynamic conditions within the body. As a result, it holds the potential for applications in precision and personalized medicine. However, there are still limitations in sequential development processes and complex structures, resulting in time-consuming molecular interference during system development. In this study, we developed a channel-assembling tumor microenvironment-on-chip (CATOC) system to overcome these limitations. CATOC was easily segmented into blood vessels and a tumor microenvironment-on-chip, which can be independently developed. The tumor microenvironment-on-chip consists of two independent channels for evaluating drug responses in different types of tumor microenvironments. Each fully developed system was physically interconnected to create a CATOC. Interconnected CATOC was used to validate chemical and targeted anticancer drug responses in different subtypes of the breast tumor microenvironment. We also emphasized the significance of on-chip experiments by observing the drug response of tumor spheroids on CATOC and scaffold-free platforms.
引用
收藏
页码:376 / 384
页数:9
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