Feng Hao, Ou Bao-Chi, Zhao Jing-Kun, Yin Shuai, Lu Ai-Guo, Oechsle Eva, Thasler Wolfgang E
Department of Digestive Surgery, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, 200025, Shanghai, China.
Medical Faculty, University Hospital of LMU Munich, 81377, Munich, Germany.
J Cancer Res Clin Oncol. 2017 Sep;143(9):1771-1786. doi: 10.1007/s00432-017-2434-2. Epub 2017 May 11.
Pancreatic cancer 3D in vitro models including multicellular tumor spheroid (MCTS), single cell-derived tumor spheroid (SCTS), tissue-derived tumor spheroid, and organotypic models provided powerful platforms to mimic in vivo tumor. Recent work supports that circulating tumor cell (CTC) clusters are more efficient in metastasis seeding than single CTCs. The purpose of this study is to establish 3D culture models which can mimic single CTC, monoclonal CTC clusters, and the expansion of macrometastases.
Seven pancreatic ductal adenocarcinoma cell lines were used to establish MCTS and SCTS using hanging drop and ultra-low attachment plates. Spheroid immunofluorescence staining, spheroid formation assay, immunoblotting, and literature review were performed to investigate molecular biomarkers and the morphological characteristics of pancreatic tumor spheroids.
Single cells experienced different growth patterns to form SCTS, like signet ring-like cells, blastula-like structures, and solid core spheroids. However, golf ball-like hollow spheroids could also be detected, especially when DanG and Capan-1 cells were cultivated with fibroblast-conditioned medium (p < 0.05). The size of golf ball-like hollow spheroids hardly grew after getting matured. Only DanG and Capan-1 could establish SCTS- and MCTS-derived hollow spheroids using hanging drop plates and ultra-low attachment plates. Other PDA cell lines could also establish tumor spheroid with hanging drop plates by adding methylated cellulose. Tumor spheroids derived from pancreatic cancer cell line DanG possessed asymmetrically distributed proliferation center, immune-checkpoint properties. ß-catenin, Ki-67, and F-actin were active surrounding the crater-like structure distributing on the inner layer of viable rim cover of the spheroids, which was relevant to well-differentiated tumor cells.
It is possible to establish 3D CTC cluster models from homogenous PDA cell lines using hanging drop and ultra-low attachment plates. PDA cell line displays its own intrinsic properties or heterogeneity. The mechanism of formation of the crater-like structure as well as golf ball-like structure needs further exploration.
胰腺癌的三维体外模型,包括多细胞肿瘤球(MCTS)、单细胞衍生肿瘤球(SCTS)、组织衍生肿瘤球和器官型模型,为模拟体内肿瘤提供了强大的平台。最近的研究支持循环肿瘤细胞(CTC)簇在转移播种方面比单个CTC更有效。本研究的目的是建立能够模拟单个CTC、单克隆CTC簇以及大转移灶扩展的三维培养模型。
使用七种胰腺导管腺癌细胞系,通过悬滴法和超低吸附板建立MCTS和SCTS。进行球状体免疫荧光染色、球状体形成试验、免疫印迹和文献综述,以研究胰腺肿瘤球状体的分子生物标志物和形态特征。
单个细胞经历不同的生长模式形成SCTS,如印戒样细胞、囊胚样结构和实心核心球状体。然而,也可以检测到高尔夫球样空心球状体,尤其是当DanG和Capan-1细胞与成纤维细胞条件培养基一起培养时(p < 0.05)。高尔夫球样空心球状体成熟后大小几乎不再增长。只有DanG和Capan-1能够使用悬滴板和超低吸附板建立SCTS和MCTS衍生的空心球状体。其他PDA细胞系也可以通过添加甲基纤维素用悬滴板建立肿瘤球状体。源自胰腺癌细胞系DanG的肿瘤球状体具有不对称分布的增殖中心、免疫检查点特性。β-连环蛋白、Ki-67和F-肌动蛋白在球状体活边缘覆盖层内层分布的火山口样结构周围活跃,这与高分化肿瘤细胞有关。
使用悬滴板和超低吸附板从同质PDA细胞系建立三维CTC簇模型是可能的。PDA细胞系表现出其自身的内在特性或异质性。火山口样结构以及高尔夫球样结构的形成机制需要进一步探索。