PO.TB04.07 · 肿瘤生物学

生物打印的结直肠癌类器官作为大规模治疗筛选平台

Bioprinted colorectal cancer organoids as a platform for large-scale therapeutic screening

编号 3421 展板 26 时间 4/20 02:00–05:00 区域 Section 28 主讲 Taehee Kim, BS;MS
分会场 In Vitro Models 1: 2D and 3D
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作者与单位 Authors & Affiliations

Taehee Kim, Jonathan Levi, Catherine Chen, Lindsay Ng, Alice Soragni

UCLA - University of California Los Angeles, Los Angeles, CA

摘要 Abstract

中文摘要
结直肠癌是美国癌症相关死亡的第四大原因。在转移性结直肠癌患者中,约70-75%在诊断后存活超过1年,30-35%存活超过3年,不到20%存活超过5年。不可切除转移性结直肠癌的主要治疗选择包括细胞毒性化疗、生物制剂、免疫治疗及其组合。不可切除转移性疾病的治疗选择仍然有限,迫切需要更具预测性的临床前平台。为满足这一需求,我们开发了一种高通量微环筛选平台,使用通过3D生物打印生成的患者来源结直肠癌类器官。我们生成并筛选了超过28,000个生物打印类器官微环,以确保各模型间尺寸、结构和可重现性的一致性。筛选纳入了标准结直肠癌药物,包括5-氟尿嘧啶、卡培他滨、伊立替康、亚叶酸钙和奥沙利铂,以及一个涵盖多种通路的100种化合物的靶向组合。剂量反应分析实现了稳健的IC50测定,并揭示了代表多个疾病阶段的类器官模型间不同的敏感性和耐药模式。整合了每个模型的转录组分析,以将这些功能特征置于背景中并识别与治疗易感性相关的通路水平特征。这项工作展示了生物打印的结直肠癌类器官如何提供一个可扩展且具生物相关性的平台,用于高通量药物筛选,以支持开发更精确有效的结直肠癌治疗策略。
查看英文原文 English abstract
Colorectal cancer is the fourth leading cause of cancer-related deaths in the United States. Among patients with metastatic colorectal cancer, approximately 70-75% survive more than 1 year after diagnosis, 30-35% survive more than 3 years, and fewer than 20% survive beyond 5 years. The main treatment options for unresectable metastatic colorectal cancer include cytotoxic chemotherapy, biologics, immunotherapy, and combinations thereof. Therapeutic options for unresectable metastatic disease remain limited, and more predictive preclinical platforms are urgently needed. To address this need, we developed a high-throughput mini-ring screening platform using patient-derived colorectal cancer organoids generated through 3D bioprinting. We generated and screened more than 28,000 bioprinted organoid mini-rings to ensure uniform size, architecture, and reproducibility across models.Screens incorporated standard colorectal cancer agents, including 5-fluorouracil, capecitabine, irinotecan, leucovorin, and oxaliplatin, along with a targeted 100-compound targeted panel spanning diverse pathways. Dose-response profiling enabled robust IC50 determination and revealed distinct sensitivity and resistance patterns across organoid models representing multiple disease stages. Transcriptomic analyses for each model were integrated to contextualize these functional profiles and identify pathway-level features associated with therapeutic vulnerability.This work shows how bioprinted colorectal cancer organoids provide a scalable and biologically relevant platform for high-throughput drug screening to support the development of more precise and effective therapeutic strategies for colorectal cancer.
利益披露 Disclosure
T. Kim, None.. J. Levi, None.. C. Chen, None.. L. Ng, None.. A. Soragni, None.

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