3D Collagen Vascular Tumor-on-a-Chip Mimetics for Dynamic Combinatorial Drug Screening

被引:10
作者
Wan, Li [1 ]
Yin, Jun [2 ]
Skoko, John [3 ]
Schwartz, Russell [4 ]
Zhang, Mei [2 ]
LeDuc, Philip R. [1 ]
Neumann, Carola A. [3 ]
机构
[1] Carnegie Mellon Univ, Dept Mech Engn, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Med Ctr, Dept Dev Biol, Canc Inst,Magee Womens Res Inst, Pittsburgh, PA 15213 USA
[3] Univ Pittsburgh, Med Ctr, Dept Pharmacol & Chem Biol, Canc Inst,Magee Womens Res Inst, Pittsburgh, PA 15213 USA
[4] Carnegie Mellon Univ, Computat Biol Dept, Pittsburgh, PA 15213 USA
关键词
CELL-CULTURE; BREAST-CANCER; BIWEEKLY PACLITAXEL; EXPERIMENTAL-DESIGN; PHASE-II; CYCLOPHOSPHAMIDE; DOXORUBICIN; CISPLATIN; GROWTH; TRIAL;
D O I
10.1158/1535-7163.MCT-20-0880
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Disease models, including in vitro cell culture and animal models, have contributed significantly to developing diagnostics and treatments over the past several decades. The successes of traditional drug screening methods were generally hampered by not adequately mimicking critical in vivo features, such as a 3D microenvironment and dynamic drug diffusion through the extracellular matrix (ECM). To address these issues, we developed a 3D dynamic drug delivery system for cancer drug screening that mimicks drug dissemination through the tumor vasculature and the ECM by creating collagen-embedded microfluidic channels. Using this novel 3D ECM microsystem, we compared viability of tumor pieces with traditionally used 2D methods in response to three different drug combinations. Drug diffusion profiles were evaluated by simulation methods and tested in the 3D ECM microsystem and a 2D 96-well setup. Compared with the 2D control, the 3D ECM microsystem produced reliable data on viability, drug ratios, and combination indeces. This novel approach enables higher throughput and sets the stage for future applications utilizing drug sensitivity predicting algorithms based on dynamic diffusion profiles requiring only minimal patient tissue. Our findings moved drug sensitivity screening closer to clinical implications with a focus on testing combinatorial drug effects, an option often limited by the amount of available patient tissues.
引用
收藏
页码:1210 / 1219
页数:10
相关论文
共 56 条
[1]   Cell culture: Biology's new dimension [J].
Abbott, A .
NATURE, 2003, 424 (6951) :870-872
[2]  
Abujamra AL, 2011, DIAGNOSTIC TECHNIQUE
[3]  
ALBERTS DS, 1984, INVEST NEW DRUG, V2, P141
[4]   3D microfluidic ex vivo culture of organotypic tumor spheroids to model immune checkpoint blockade [J].
Aref, Amir R. ;
Campisi, Marco ;
Ivanova, Elena ;
Portell, Andrew ;
Larios, Dalia ;
Piel, Brandon P. ;
Mathur, Natasha ;
Zhou, Chensheng ;
Coakley, Raven Vlahos ;
Bartels, Alan ;
Bowden, Michaela ;
Herbert, Zach ;
Hill, Sarah ;
Gilhooley, Sean ;
Carter, Jacob ;
Canadas, Israel ;
Thai, Tran C. ;
Kitajima, Shunsuke ;
Chiono, Valeria ;
Paweletz, Cloud P. ;
Barbie, David A. ;
Kamm, Roger D. ;
Jenkins, Russell W. .
LAB ON A CHIP, 2018, 18 (20) :3129-3143
[5]   Engineering cancer microenvironments for in vitro 3-D tumor models [J].
Asghar, Waseem ;
El Assal, Rami ;
Shafiee, Hadi ;
Pitteri, Sharon ;
Paulmurugan, Ramasamy ;
Demirci, Utkan .
MATERIALS TODAY, 2015, 18 (10) :539-553
[6]  
BASTERT G, 1976, Z KREBSFORSCH KLIN O, V85, P299
[7]   Raise standards for preclinical cancer research [J].
Begley, C. Glenn ;
Ellis, Lee M. .
NATURE, 2012, 483 (7391) :531-533
[8]   The upcoming 3D-printing revolution in microfluidics [J].
Bhattacharjee, Nirveek ;
Urrios, Arturo ;
Kanga, Shawn ;
Folch, Albert .
LAB ON A CHIP, 2016, 16 (10) :1720-1742
[9]   Doxorubicin targets multiple players: A new view of an old problem [J].
Cappetta, Donato ;
Rossi, Francesca ;
Piegari, Elena ;
Quaini, Federico ;
Berrino, Liberato ;
Urbanek, Konrad ;
De Angelis, Antonella .
PHARMACOLOGICAL RESEARCH, 2018, 127 :4-14
[10]   Parallel microfluidic chemosensitivity testing on individual slice cultures [J].
Chang, Tim C. ;
Mikheev, Andrei M. ;
Wilson Huynh ;
Monnat, Raymond J., Jr. ;
Rostomily, Robert C. ;
Folch, Albert .
LAB ON A CHIP, 2014, 14 (23) :4540-4551