Automated Analysis of Extracellular Matrix Invasion of Cancer Cells from Tumor Spheroids

被引:2
作者
Heiss, Jacob [1 ]
Tavana, Hossein [1 ]
机构
[1] Univ Akron, Dept Biomed Engn, Akron, OH 44325 USA
来源
ACS MEASUREMENT SCIENCE AU | 2023年 / 4卷 / 03期
关键词
breast cancer; image analysis; cancer invasion; automation; tumor model; MIGRATION;
D O I
10.1021/acsmeasuresciau.3c00064
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The main cause of mortality among cancer patients is metastatic disease. Metastasis develops from cancer cells that invade the stromal tissue and intravasate the circulatory or lymphatic systems to eventually form new tumors in other organs. Blocking cancer cell invasion can potentially prevent or reduce the metastatic progression of cancers. Testing different chemical compounds against cell invasion in three-dimensional cultures is a common laboratory technique. The efficacy of the treatments is often evaluated from confocal microscopic images of the cells using image processing. However, the analysis approaches are often subject to variations and inconsistencies due to user decisions that must be made while processing each image. To overcome this limitation, we developed a fully automated method to quantify the invasion of cancer cells from a 3D tumor spheroid into the surrounding extracellular matrix. We demonstrated that this method resolves cell invasion from spheroids of different shapes and sizes and from cells that invade as a cluster or individually. We also showed that this approach can help quantify the dose-dependent anti-invasive effects of a commonly used chemotherapy drug. Our automated method significantly reduces the time and increases the consistency and accuracy of cancer cell invasion analysis in three-dimensional cultures.
引用
收藏
页码:260 / 266
页数:7
相关论文
共 30 条
[1]   High Throughput, Polymeric Aqueous Two-Phase Printing of Tumor Spheroids [J].
Atefi, Ehsan ;
Lemmo, Stephanie ;
Fyffe, Darcy ;
Luker, Gary D. ;
Tavana, Hossein .
ADVANCED FUNCTIONAL MATERIALS, 2014, 24 (41) :6509-6515
[2]   Dynamic EMT: a multi-tool for tumor progression [J].
Brabletz, Simone ;
Schuhwerk, Harald ;
Brabletz, Thomas ;
Stemmler, Marc P. .
EMBO JOURNAL, 2021, 40 (18)
[3]   Targeting disseminated estrogen-receptor-positive breast cancer cells in bone marrow [J].
Buschhaus, Johanna M. ;
Humphries, Brock A. ;
Eckley, Samantha S. ;
Robison, Tanner H. ;
Cutter, Alyssa C. ;
Rajendran, Shrila ;
Haley, Henry R. ;
Bevoor, Avinash S. ;
Luker, Kathryn E. ;
Luker, Gary D. .
ONCOGENE, 2020, 39 (34) :5649-5662
[4]   High-throughput Image Analysis of Tumor Spheroids: A User-friendly Software Application to Measure the Size of Spheroids Automatically and Accurately [J].
Chen, Wenjin ;
Wong, Chung ;
Vosburgh, Evan ;
Levine, Arnold J. ;
Foran, David J. ;
Xu, Eugenia Y. .
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS, 2014, (89)
[5]  
Conti S, 2021, METHODS MOL BIOL, V2179, P243, DOI 10.1007/978-1-0716-0779-4_19
[6]   The Use of Microfluidic Platforms to Probe the Mechanism of Cancer Cell Extravasation [J].
Coughlin, Mark F. ;
Kamm, Roger D. .
ADVANCED HEALTHCARE MATERIALS, 2020, 9 (08)
[7]   Morphologic instability and cancer invasion [J].
Cristini, V ;
Frieboes, HB ;
Gatenby, R ;
Caserta, S ;
Ferrari, M ;
Sinek, J .
CLINICAL CANCER RESEARCH, 2005, 11 (19) :6772-6779
[8]   Chemotherapy-Induced Collagen IV Drives Cancer Cell Motility through Activation of Src and Focal Adhesion Kinase [J].
Fatherree, Jackson P. ;
Guarin, Justinne R. ;
McGinn, Rachel A. ;
Naber, Stephen P. ;
Oudin, Madeleine J. .
CANCER RESEARCH, 2022, 82 (10) :2031-2044
[9]   The amoeboid state as part of the epithelial-to-mesenchymal transition programme [J].
Graziani, Vittoria ;
Rodriguez-Hernandez, Irene ;
Maiques, Oscar ;
Sanz-Moreno, Victoria .
TRENDS IN CELL BIOLOGY, 2022, 32 (03) :228-242
[10]   Molecular characterisation of cell line models for triple-negative breast cancers [J].
Grigoriadis, Anita ;
Mackay, Alan ;
Noel, Elodie ;
Wu, Pei Jun ;
Natrajan, Rachel ;
Frankum, Jessica ;
Reis-Filho, Jorge S. ;
Tutt, Andrew .
BMC GENOMICS, 2012, 13