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整体基因组与组织工程使得在生理相关可灌注的离体培养物中筛选癌症脆弱性成为可能。

Integrated genome and tissue engineering enables screening of cancer vulnerabilities in physiologically relevant perfusable ex vivo cultures.

机构信息

Department of Bioengineering, University of California San Diego, La Jolla, USA.

Tumor Initiation & Maintenance Program, NCI-Designated Cancer Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, USA.

出版信息

Biomaterials. 2022 Jan;280:121276. doi: 10.1016/j.biomaterials.2021.121276. Epub 2021 Dec 2.

Abstract

Genetic screens are powerful tools for both resolving biological function and identifying potential therapeutic targets, but require physiologically accurate systems to glean biologically useful information. Here, we enable genetic screens in physiologically relevant ex vivo cancer tissue models by integrating CRISPR-Cas-based genome engineering and biofabrication technologies. We first present a novel method for generating perfusable tissue constructs, and validate its functionality by using it to generate three-dimensional perfusable dense cultures of cancer cell lines and sustain otherwise ex vivo unculturable patient-derived xenografts. Using this system we enable large-scale CRISPR screens in perfused tissue cultures, as well as emulate a novel point-of-care diagnostics scenario of a clinically actionable CRISPR knockout (CRISPRko) screen of genes with FDA-approved drug treatments in ex vivo PDX cell cultures. Our results reveal differences across in vitro and in vivo cancer model systems, and highlight the utility of programmable tissue engineered models for screening therapeutically relevant cancer vulnerabilities.

摘要

遗传筛选是解决生物学功能和确定潜在治疗靶点的有力工具,但需要生理上准确的系统来获取有生物学意义的信息。在这里,我们通过整合基于 CRISPR-Cas 的基因组工程和生物制造技术,在生理相关的离体癌症组织模型中实现了遗传筛选。我们首先提出了一种生成可灌注组织构建体的新方法,并通过使用该方法生成了三种癌细胞系的可灌注三维致密培养物并维持了否则无法在体外培养的患者来源异种移植物,验证了其功能。使用该系统,我们能够在灌注组织培养物中进行大规模的 CRISPR 筛选,并且能够模拟一种新的即时护理诊断场景,即对具有 FDA 批准药物治疗的基因进行临床可操作的 CRISPR 敲除 (CRISPRko) 筛选离体 PDX 细胞培养物。我们的结果揭示了体外和体内癌症模型系统之间的差异,并强调了可编程组织工程模型在筛选治疗相关癌症脆弱性方面的实用性。

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