Crouchet Emilie, Almeida Nuno, Durand Sarah C, Parnot Marie, Oudot Marine A, Giannone Fabio, Gadenne Cloé, Roehlen Natascha, Saviano Antonio, Felli Emanuele, Pessaux Patrick, Duong Hong Tuan, Ohdan Hideki, Aikata Hiroshi, Chayama Kazuaki, Baumert Thomas F, Schuster Catherine
University of Strasbourg, Inserm, Institute for Translational Medicine and Liver Disease UMR S1110, Strasbourg, France.
Hepato-Pancreato-Biliary, Oncologic and Robotic Unit, Azienda Ospedaliero-Universitaria SS, Antonio e Biagio e Cesare Arrigo, Alessandria, Italy.
JHEP Rep. 2024 Oct 28;7(2):101252. doi: 10.1016/j.jhepr.2024.101252. eCollection 2025 Feb.
BACKGROUND & AIMS: Hepatocellular carcinoma (HCC) is the third-leading and fastest rising cause of cancer-related death worldwide. The discovery and preclinical development of compounds targeting HCC are hampered by the absence of authentic tractable systems recapitulating the heterogeneity of HCC tumors in patients and the tumor microenvironment (TME).
We established a novel and simple patient-derived multicellular tumor spheroid model based on clinical HCC tumor tissues, processed using enzymatic and mechanical dissociation. After quality controls, 22 HCC tissues and 17 HCC sera were selected for tumor spheroid generation and perturbation studies. Cells were grown in 3D in optimized medium in the presence of patient serum. Characterization of the tumor spheroid cell populations was performed by flow cytometry, immunohistochemistry (IHC), and functional assays. As a proof of concept, we treated patient-derived spheroids with FDA-approved anti-HCC compounds.
The model was successfully established independently from cancer etiology and grade from 22 HCC tissues. The use of serum from patients with HCC was essential for tumor spheroid generation, TME function, and maintenance of cell viability. The tumor spheroids comprised the main cell compartments, including epithelial cancer cells, as well as all major cell populations of the TME [ cancer-associated fibroblasts (CAFs), macrophages, T cells, and endothelial cells]. Tumor spheroids reflected HCC heterogeneity, including variability in cell type proportions and TME, and mimicked the original tumor features. Moreover, differential responses to FDA-approved anti-HCC drugs were observed between the donors, as observed in patients.
This patient HCC serum-tumor spheroid model provides novel opportunities for drug discovery and development as well as mechanism-of-action studies including compounds targeting the TME. This model will likely contribute to improve the therapeutic outcomes for patients with HCC.
HCC is a leading and fast-rising cause of cancer-related death worldwide. Despite approval of novel therapies, the outcome of advanced HCC remains unsatisfactory. By developing a novel patient-derived tumor spheroid model recapitulating tumor heterogeneity and microenvironment, we provide new opportunities for HCC drug development and analysis of mechanism of action in authentic patient tissues. The application of the patient-derived tumor spheroids combined with other HCC models will likely contribute to drug development and to improve the outcome of patients with HCC.
肝细胞癌(HCC)是全球癌症相关死亡的第三大且增长最快的原因。由于缺乏能够再现患者HCC肿瘤异质性和肿瘤微环境(TME)的真实且易于处理的系统,靶向HCC的化合物的发现和临床前开发受到阻碍。
我们基于临床HCC肿瘤组织建立了一种新颖且简单的患者来源的多细胞肿瘤球体模型,通过酶解和机械解离进行处理。经过质量控制后,选择22个HCC组织和17份HCC血清用于肿瘤球体的生成和干扰研究。细胞在含有患者血清的优化培养基中进行三维培养。通过流式细胞术、免疫组织化学(IHC)和功能测定对肿瘤球体细胞群体进行表征。作为概念验证,我们用FDA批准的抗HCC化合物处理患者来源的球体。
该模型成功地从22个HCC组织独立建立,与癌症病因和分级无关。使用HCC患者的血清对于肿瘤球体的生成、TME功能和细胞活力的维持至关重要。肿瘤球体包含主要的细胞成分,包括上皮癌细胞,以及TME的所有主要细胞群体[癌症相关成纤维细胞(CAF)、巨噬细胞、T细胞和内皮细胞]。肿瘤球体反映了HCC的异质性,包括细胞类型比例和TME的变异性,并模拟了原始肿瘤特征。此外,正如在患者中观察到的那样,在供体之间观察到了对FDA批准的抗HCC药物的不同反应。
这种患者HCC血清 - 肿瘤球体模型为药物发现和开发以及包括靶向TME的化合物在内的作用机制研究提供了新的机会。该模型可能有助于改善HCC患者的治疗效果。
HCC是全球癌症相关死亡的主要且快速上升的原因。尽管新型疗法已获批准,但晚期HCC的治疗结果仍不尽人意。通过开发一种能够再现肿瘤异质性和微环境的新型患者来源的肿瘤球体模型,我们为HCC药物开发和在真实患者组织中分析作用机制提供了新的机会。患者来源的肿瘤球体与其他HCC模型的联合应用可能有助于药物开发并改善HCC患者的治疗结果。