Giron-Michel Julien, Padelli Maël, Oberlin Estelle, Guenou Hind, Duclos-Vallée Jean-Charles
INSERM UMR-S-MD 1197, Paul-Brousse Hospital, Villejuif, France.
Orsay-Vallée Campus, Paris-Saclay University, Gif-sur-Yvette, France.
BioDrugs. 2025 Mar;39(2):237-260. doi: 10.1007/s40259-024-00702-0. Epub 2025 Jan 18.
Liver cancer poses a global health challenge with limited therapeutic options. Notably, the limited success of current therapies in patients with primary liver cancers (PLCs) may be attributed to the high heterogeneity of both hepatocellular carcinoma (HCCs) and intrahepatic cholangiocarcinoma (iCCAs). This heterogeneity evolves over time as tumor-initiating stem cells, or cancer stem cells (CSCs), undergo (epi)genetic alterations or encounter microenvironmental changes within the tumor microenvironment. These modifications enable CSCs to exhibit plasticity, differentiating into various resistant tumor cell types. Addressing this challenge requires urgent efforts to develop personalized treatments guided by biomarkers, with a specific focus on targeting CSCs. The lack of effective precision treatments for PLCs is partly due to the scarcity of ex vivo preclinical models that accurately capture the complexity of CSC-related tumors and can predict therapeutic responses. Fortunately, recent advancements in the establishment of patient-derived liver cancer cell lines and organoids have opened new avenues for precision medicine research. Notably, patient-derived organoid (PDO) cultures have demonstrated self-assembly and self-renewal capabilities, retaining essential characteristics of their respective in vivo tissues, including both inter- and intratumoral heterogeneities. The emergence of PDOs derived from PLCs serves as patient avatars, enabling preclinical investigations for patient stratification, screening of anticancer drugs, efficacy testing, and thereby advancing the field of precision medicine. This review offers a comprehensive summary of the advancements in constructing PLC-derived PDO models. Emphasis is placed on the role of CSCs, which not only contribute significantly to the establishment of PDO cultures but also faithfully capture tumor heterogeneity and the ensuing development of therapy resistance. The exploration of PDOs' benefits in personalized medicine research is undertaken, including a discussion of their limitations, particularly in terms of culture conditions, reproducibility, and scalability.
肝癌对全球健康构成挑战,治疗选择有限。值得注意的是,目前针对原发性肝癌(PLC)患者的治疗效果有限,这可能归因于肝细胞癌(HCC)和肝内胆管癌(iCCA)的高度异质性。随着肿瘤起始干细胞或癌症干细胞(CSC)发生(表观)遗传改变或在肿瘤微环境中遭遇微环境变化,这种异质性会随时间演变。这些改变使CSC表现出可塑性,分化为各种耐药肿瘤细胞类型。应对这一挑战需要迫切努力开发以生物标志物为导向的个性化治疗方法,特别关注靶向CSC。PLC缺乏有效的精准治疗部分原因是缺乏能够准确捕捉CSC相关肿瘤复杂性并预测治疗反应的体外临床前模型。幸运的是,最近在建立患者来源的肝癌细胞系和类器官方面取得的进展为精准医学研究开辟了新途径。值得注意的是,患者来源的类器官(PDO)培养物已证明具有自我组装和自我更新能力,保留了其各自体内组织的基本特征,包括肿瘤间和肿瘤内的异质性。源自PLC的PDO的出现充当了患者替身,能够进行临床前研究以进行患者分层、抗癌药物筛选、疗效测试,从而推动精准医学领域的发展。本综述全面总结了构建源自PLC的PDO模型的进展。重点强调了CSC的作用,CSC不仅对PDO培养物的建立有重大贡献,还能忠实地捕捉肿瘤异质性以及随之而来的治疗耐药性发展。本文探讨了PDO在个性化医学研究中的益处,包括讨论其局限性,特别是在培养条件、可重复性和可扩展性方面。