Breast cancer PDxO cultures for drug discovery and functional precision oncology

被引:6
|
作者
Scherer, Sandra D. [1 ,2 ]
Zhao, Ling [1 ,2 ]
Butterfield, Andrew J. [1 ,2 ]
Yang, Chieh-Hsiang [1 ,2 ]
Cortes-Sanchez, Emilio [1 ,2 ]
Guillen, Katrin P. [1 ]
Welm, Bryan E. [1 ,3 ]
Welm, Alana L. [1 ,2 ]
机构
[1] Univ Utah, Huntsman Canc Inst, 2000 Circle Hope, Salt Lake City, UT 84112 USA
[2] Univ Utah, Dept Oncol Sci, 2000 Circle Hope, Salt Lake City, UT 84112 USA
[3] Univ Utah, Dept Surg, 30 N 1900 E, Salt Lake City, UT 84132 USA
来源
STAR PROTOCOLS | 2023年 / 4卷 / 03期
基金
美国国家卫生研究院;
关键词
Cancer; Cell Culture; Cell-based Assays; Model Organisms; Organoids;
D O I
10.1016/j.xpro.2023.102402
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Patient-derived xenografts (PDXs) have clinical value but are time-, cost-, and labor-intensive and thus ill-suited for large-scale experiments. Here, we present a protocol to convert PDX tumors into PDxOs for long-term cultures amenable to moderate-throughput drug screens, including in-depth PDxO validation. We describe steps for PDxO preparation and mouse cell removal. We then detail PDxO validation and characterization and drug response assay. Our PDxO drug screening platform can predict therapy response in vivo and inform functional precision oncology for patients.For complete details on the use and execution of this protocol, please refer to Guillen et al.1
引用
收藏
页数:43
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