Next-generation cancer organoids

被引:234
作者
LeSavage, Bauer L. [1 ]
Suhar, Riley A. [2 ]
Broguiere, Nicolas [3 ,4 ,5 ]
Lutolf, Matthias P. [3 ,4 ,5 ]
Heilshorn, Sarah C. [2 ]
机构
[1] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Mat Sci & Engn, Stanford, CA 94305 USA
[3] Ecole Polytech Fed Lausanne EPFL, Lab Stem Cell Bioengn, Inst Bioengn, Sch Life Sci, Lausanne, Switzerland
[4] Ecole Polytech Fed Lausanne EPFL, Sch Engn, Lausanne, Switzerland
[5] Ecole Polytech Fed Lausanne EPFL, Sch Basic Sci, Inst Chem Sci & Engn, Lausanne, Switzerland
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
MODELING COLORECTAL-CANCER; PATIENT-DERIVED ORGANOIDS; PLURIPOTENT STEM-CELLS; EXTRACELLULAR-MATRIX; TUMOR HETEROGENEITY; IN-VITRO; 3D CULTURE; GROWTH; NICHE; RESISTANCE;
D O I
10.1038/s41563-021-01057-5
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Organotypic models of patient-specific tumours are revolutionizing our understanding of cancer heterogeneity and its implications for personalized medicine. These advancements are, in part, attributed to the ability of organoid models to stably preserve genetic, proteomic, morphological and pharmacotypic features of the parent tumour in vitro, while also offering unprecedented genomic and environmental manipulation. Despite recent innovations in organoid protocols, current techniques for cancer organoid culture are inherently uncontrolled and irreproducible, owing to several non-standardized facets including cancer tissue sources and subsequent processing, medium formulations, and animal-derived three-dimensional matrices. Given the potential for cancer organoids to accurately recapitulate the intra- and intertumoral biological heterogeneity associated with patient-specific cancers, eliminating the undesirable technical variability accompanying cancer organoid culture is necessary to establish reproducible platforms that accelerate translatable insights into patient care. Here we describe the current challenges and recent multidisciplinary advancements and opportunities for standardizing next-generation cancer organoid systems. This Review summarizes limitations in the current techniques used for patient-derived cancer organoid culture and highlights recent advancements and future opportunities for their standardization.
引用
收藏
页码:143 / 159
页数:17
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