PO.TB04.08 · 肿瘤生物学

用于转化癌症研究的多癌种患者来源类器官平台

Multi-cancer patient-derived organoid platform for translational cancer research

海报缩略图:用于转化癌症研究的多癌种患者来源类器官平台
编号 7532 展板 13 时间 4/22 09:00–12:00 区域 Section 32 主讲 Jubi Heo, MS
分会场 Tumor Models and Assays: In Vitro, In Vivo
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作者与单位 Authors & Affiliations

JUBI HEO1, Choong-Jae LEE1, Eun Joo LEE1, Sung Weon Choi2, Sang-Jae Park3, Sang Myung Woo3, Sang Yoon Park4, Myong Cheol Lim4, So-Youn Jung5, Bo Hyun Kim3, Jung Won Chun3, Joohyun Hong6, Wonyoung Choi1, Sun-Young Kong1

1Targeted Therapy Branch, National Cancer Center(NCC), Goyang, Korea, Republic of,2Department of Oral and Maxilofacial Surgery, National Cancer Center(NCC), Goyang, Korea, Republic of,3Center for Liver and Pancreatobiliary Cancer, National Cancer Center(NCC), Goyang, Korea, Republic of,4Center for Gynecologic Cancer, National Cancer Center(NCC), Goyang, Korea, Republic of,5Center for Breast Cancer, National Cancer Center(NCC), Goyang, Korea, Republic of,6Center for Colorectal Cancer, National Cancer Center(NCC), Goyang, Korea, Republic of

摘要 Abstract

中文摘要
目的:患者来源类器官(PDO)是有用的癌症模型,因为它们反映了每位患者肿瘤的重要特征。然而在韩国,研究人员一直缺乏具有明确临床信息的充足PDO样本。为改善这一状况,国立癌症中心建立了一个平台,以收集来自不同癌种的类器官,并提供可用于研究的可靠模型。 方法:肿瘤标本通过手术切除、影像引导活检及恶性体液获取。所有样本均采用统一的工作流程处理,涵盖组织处理、酶解分离、类器官培养及长期生长的标准。持续生长超过五代的PDO被判定为成功建立。质量检查包括STR分型、支原体检测以及组织学和基因组学评估,以确保准确性和安全性。临床和病理信息与每个PDO相关联,并采用生物样本库程序进行长期储存。选定的模型采用384孔筛选形式在药物反应检测中进行评估。 结果:该平台目前维持着涵盖多种癌型的122个PDO模型,包括口腔癌(n = 33)、胰腺癌(n = 20)、舌癌(n = 16)、胃癌(n = 16)、卵巢癌(n = 9)、胆囊癌(n = 8)、胆道癌(n = 8)、乳腺癌(n = 5)、肝癌(n = 4)和结直肠癌(n = 3)。这些PDO保留了其匹配肿瘤的关键组织病理学、遗传学和表型特征,并成功冷冻保存以供长期使用。对42个PDO使用46种治疗药物进行的药物反应分析揭示了显著的肿瘤间变异性,且若干在研化合物表现出显著的抗肿瘤活性。在代表性病例中,离体细胞毒性反应与临床治疗结局相符,凸显了该平台的转化相关性。 结论:该PDO平台提供了一个集中化的高质量资源,反映了人类癌症的生物学和临床多样性。通过支持系统性药物筛选、机制研究及基于生物标志物的精准方法,该平台为推进转化肿瘤学研究、促进韩国个体化治疗策略的开发提供了必要的基础设施。本研究由韩国政府(MSIT)资助的国家研究基金会(NRF)生物与医学技术开发计划支持(编号:RS-2025-19542979)。
查看英文原文 English abstract
Purpose Patient-derived organoids (PDOs) are useful cancer models because they reflect important features of each patient's tumor. In Korea, however, researchers have not had enough PDO samples with clear clinical information. To improve this situation, the National Cancer Center created a platform to collect organoids from different cancers and provide reliable models that can be used for research. Methods Tumor specimens were obtained through surgical resection, image-guided biopsy, and malignant body fluids. All samples were processed using a unified workflow covering tissue handling, enzymatic dissociation, organoid culture, and criteria for long-term growth. PDOs that continued to grow for more than five passages were classified as successfully established. Quality checks included STR profiling, mycoplasma testing, and histologic and genomic evaluation to ensure accuracy and safety. Clinical and pathological information was linked to each PDO, and biobanking procedures were used for long-term storage. Selected models were evaluated in drug-response assays using a 384-well screening format. Results The platform currently maintains 122 PDO models across multiple cancer types, including oral (n = 33), pancreatic (n = 20), tongue (n = 16), gastric (n = 16), ovarian (n = 9), gallbladder (n = 8), biliary tract (n = 8), breast (n = 5), liver (n = 4), and colorectal cancers (n = 3). These PDOs preserved key histopathologic, genetic, and phenotypic characteristics of their matched tumors and were successfully cryopreserved for long-term use. Drug-response profiling of 42 PDOs with 46 therapeutic agents revealed substantial inter-tumoral variability, and several investigational compounds demonstrated notable antitumor activity. In representative cases, ex vivo cytotoxic responses corresponded with clinical treatment outcomes, underscoring the translational relevance of the platform. Conclusions This PDO platform provides a centralized and high-quality resource that reflects the biological and clinical diversity of human cancers. By supporting systematic drug screening, mechanistic studies, and biomarker-based precision approaches, the platform offers essential infrastructure to advance translational oncology research and promote the development of personalized therapeutic strategies in Korea. This research was supported by the Bio&Medical Technology Development Program of the National Research Foundation (NRF) funded by the Korean government (MSIT) (No. RS-2025-19542979)
利益披露 Disclosure
J. Heo, None.. C. Lee, None.. E. Lee, None.. S. Choi, None.. S. Park, None.. S. Woo, None.. S. Park, None.. M. Lim, None.. S. Jung, None.. B. Kim, None.. J. Chun, None.. J. Hong, None.. W. Choi, None.. S. Kong, None.

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