在国家肿瘤医学研究中心进行肺癌原代细胞培养收集的实践经验

I. Mezhevova, A. Sitkovskaya, S. Filippova, T. V. Shamova, S. V. Timofeeva, N. Gnennaya, I. Novikova, D. Haragezov, A. Milakin, I. A. Leiman, O. Stateshny, E. Rostorguev, D. Atmachidi, T. Lapteva, M. V. Voloshin, K. S. Eremin, I. A. Suhar
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引用次数: 0

摘要

研究目的:在转化医学和生物医学中,新的化疗药物的测试需要对永生化细胞系进行研究。然而,与原代细胞培养相比,这种模型并不总是具有原位肿瘤的生物学特性。肺癌细胞原代培养物具有与活体肿瘤细胞相近或相同的生物学、形态学和分子特征。获得原发性肺癌细胞系的收集是为临床前研究创建各种模型的重要任务。材料和方法。这些材料来自25例未经治疗的新诊断的肺癌患者的术后肿瘤样本。采用以下方法获得原代培养物:在汉克斯溶液中添加300单位/ml胶原酶I (Thermo Fisher Scientific,美国),酶解法在汉克斯溶液中添加300单位/ml胶原酶I,酶解法在脑肿瘤分离试剂盒(Miltenyi Biotec,德国)中添加150单位/ml。ml的胶原酶I,以及外植体的方法。采用以下方法去除成纤维细胞:使用FibrOut™系统(CHI Scientific,美国),使用Anti-Fibroblast MicroBeads (Miltenyi Biotec,德国)磁性分离成纤维细胞,冷胰蛋白酶化。我们获得了15个通过零级传代的原发性肺癌细胞培养物。在这项工作中,酶解方法被证明是最有效的。肺肿瘤样品与胶原酶孵育1小时,可保持细胞的活力和粘附性。外植体法长期培养效果不明显,肿瘤细胞没有向塑料中迁移。磁分离是一种去除成纤维细胞基质成分效果最好的方法,同时能保持肿瘤细胞的活性。所获得的肺癌原代细胞培养物可用于实验肿瘤学的许多任务:肺癌生物学特性的研究,开发新的化疗药物的临床前模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Practical experience of a lung cancer primary cell culture collection creation at the National Medical Research Centre for Oncology
Purpose of the study. Testing of new chemotherapeutic agents in translational and biology medicine needs studies on immortalized cell lines. However, such models do not always have the biological properties of a tumor in situ, in contrast to primary cell cultures. Primary cultures of lung cancer cells have biological, morphological and molecular characteristics close or identical to tumor cells in vivo. Obtaining collections of primary lung cancer cell lines is an important task in creating various models for preclinical studies.Materials and methods. The materials are represented by postoperative tumor samples obtained from 25 patients with newly diagnosed lung cancer without prior treatment. The following methods were used to obtain primary cultures: enzymatic dissociation in Hanks' solution with the addition of 300 units/ml collagenase I (Thermo Fisher Scientific, USA), enzymatic dissociation using the Brain Tumor Dissoсiation Kit (Miltenyi Biotec, Germany) and 150 units/ml. ml of collagenase I, as well as the method of explants. The following methods were used to remove fibroblasts: the use of the FibrOut™ system (CHI Scientific, USA), magnetic separation of fibroblasts using Anti-Fibroblast MicroBeads (Miltenyi Biotec, Germany), and cold trypsinization.Results. We have obtained 15 primary lung cancer cell cultures that have passed the zero order passage. In this work, the method of enzymatic dissociation turned out to be the most effective. Incubation of lung tumor samples with collagenase for 1 hour preserves the viability and adhesiveness of the cells. The explant method did not show its effectiveness for long-term cultivation, there was no migration of tumor cells to plastic. Magnetic separation, as a method of removing stromal components of fibroblasts, showed the greatest efficiency, while maintaining the viability of tumor cells.Conclusion. The obtained primary cell cultures of lung cancer can be used for many tasks of experimental oncology: studies of the biological characteristics of lung cancer, development of preclinical models for the studies on new chemotherapeutic drugs. 
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