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
相关论文
共 50 条
  • [41] Dual-Responsive Carbon Dots for Tumor Extracellular Microenvironment Triggered Targeting and Enhanced Anticancer Drug Delivery
    Feng, Tao
    Ai, Xiangzhao
    Ong, Huimin
    Zhao, Yanli
    ACS APPLIED MATERIALS & INTERFACES, 2016, 8 (29) : 18732 - 18740
  • [42] A novel tumor-immune microenvironment (TIME)-on-Chip mimics three dimensional neutrophil-tumor dynamics and neutrophil extracellular traps (NETs)-mediated collective tumor invasion
    Surendran, Vikram
    Rutledge, Dylan
    Colmon, Ramair
    Chandrasekaran, Arvind
    BIOFABRICATION, 2021, 13 (03)
  • [43] On-Chip Organoid Formation to Study CXCR4/CXCL-12 Chemokine Microenvironment Responses for Renal Cancer Drug Testing
    Ozcelik, Adem
    Abas, Burcin Irem
    Erdogan, Omer
    Cevik, Evrim
    Cevik, Ozge
    Biosensors, 2022, 12 (12):
  • [44] On-Chip Organoid Formation to Study CXCR4/CXCL-12 Chemokine Microenvironment Responses for Renal Cancer Drug Testing
    Ozcelik, Adem
    Abas, Burcin Irem
    Erdogan, Omer
    Cevik, Evrim
    Cevik, Ozge
    BIOSENSORS-BASEL, 2022, 12 (12):
  • [45] Cutting Edge: Targeting Thrombocytes to Rewire Anticancer Immunity in the Tumor Microenvironment and Potentiate Efficacy of PD-1 Blockade
    Riesenberg, Brian P.
    Ansa-Addo, Ephraim A.
    Gutierrez, Jennifer
    Timmers, Cynthia D.
    Liu, Bei
    Li, Zihai
    JOURNAL OF IMMUNOLOGY, 2019, 203 (05): : 1105 - 1110
  • [46] Real-time and regional analysis of the efficacy of anticancer drugs in a patient-derived intratumoral heterogeneous tumor microenvironment
    Lin, Ya-Hui
    Lin, Chiao-Min
    Man, Kee-Ming
    Hung, Chih-Chiang
    Hsu, Hsin-Ling
    Chen, Yunching
    Mu, Hsuan-Yu
    Hsiao, Tzu-Hung
    Huang, Jen-Huang
    LAB ON A CHIP, 2025, 25 (07) : 1728 - 1743
  • [47] Release of Anticancer Agents in the Tumor Microenvironment Using Cathepsin B and Cathepsin L Cleavable Drug-Linker Constructs
    Deng, Yuling
    Ford, Jacob
    Maguire, Casey
    Mondal, Deboprosad
    Pinney, Kevin
    Trawick, Mary Lynn
    FASEB JOURNAL, 2021, 35
  • [48] On-chip drug testing of an aggressive intra-abdominal variant of inflammatory myofibroblastic tumor by kinase activity profiling.
    Ruijtenbeek, Rob
    van den Berg, Adrienne
    Hilhorst, Riet
    Kueffer, Stefan
    Gaiter, Timo
    Kievits, Tim
    Ebert, Matthias
    JOURNAL OF CLINICAL ONCOLOGY, 2013, 31 (15)
  • [49] Characterization of Cell-Type-Specific Drug Transport and Resistance of Breast Cancers Using Tumor-Microenvironment-on-Chip
    Shin, Kyeonggon
    Klosterhoff, Brett S.
    Han, Bumsoo
    MOLECULAR PHARMACEUTICS, 2016, 13 (07) : 2214 - 2223
  • [50] INFLUENCE OF POLYBUTYLCYANOACRYLATE NANOPARTICLES AND LIPOSOMES ON THE EFFICACY AND TOXICITY OF THE ANTICANCER DRUG MITOXANTRONE IN MURINE TUMOR-MODELS
    BECK, P
    KREUTER, J
    RESZKA, R
    FICHTNER, I
    JOURNAL OF MICROENCAPSULATION, 1993, 10 (01) : 101 - 114