Wang C T, Zhou J L, Lin G L, Yin S Y, Cong L, Zhang G N, An Y, Qiu X Y
Department of General Surgery, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing 100730, China.
State Key Laboratory of Natural and Biomimetic Drugs, Institute of Molecular Medicine, Department of Biomedical Engineering, College of Engineering, Peking University, Beijing 100080, China.
Zhonghua Zhong Liu Za Zhi. 2023 Jun 23;45(6):464-470. doi: 10.3760/cma.j.cn112152-20220928-00661.
Conventional tumor culture models include two-dimensional tumor cell cultures and xenograft models. The former has disadvantages including lack of tumor heterogeneity and poor clinical relevance, while the latter are limited by the slow growth, low engraftment successful rate, and high cost. In recent years, in vitro three-dimensional (3D) tumor models have emerged as the tool to better recapitulate the spatial structure and the environment of tumors. In addition, they preserve the pathological and genetic features of tumor cells and reflect the complex intracellular and extracellular interactions of tumors, which have become a powerful tool for investigating the tumor mechanism, drug screening, and personalized cancer treatment. 3D tumor model technologies such as spheroids, organoids, and microfluidic devices are maturing. Application of new technologies such as co-culture, 3D bioprinting, and air-liquid interface has further improved the clinical relevance of the models. Some models recapitulate the tumor microenvironment, and some can even reconstitute endogenous immune components and microvasculature. In recent years, some scholars have combined xenograft models with organoid technology to develop matched / model biobanks, giving full play to the advantages of the two technologies, and providing an ideal research platform for individualized precision therapy for specific molecular targets in certain subtypes of tumors. So far, the above technologies have been widely applied in the field of colorectal cancer research. Our research team is currently studying upon the application of patient-derived tumor cell-like clusters, a self-assembly 3D tumor model, in guiding the selection of postoperative chemotherapy regimens for colorectal cancer. A high modeling success rate and satisfactory results in the drug screening experiments have been achieved. There is no doubt that with the advancement of related technologies, 3D tumor models will play an increasingly important role in the research and clinical practice of colorectal cancer.
传统的肿瘤培养模型包括二维肿瘤细胞培养和异种移植模型。前者存在缺乏肿瘤异质性和临床相关性差等缺点,而后者则受到生长缓慢、植入成功率低和成本高的限制。近年来,体外三维(3D)肿瘤模型已成为更好地模拟肿瘤空间结构和环境的工具。此外,它们保留了肿瘤细胞的病理和遗传特征,反映了肿瘤复杂的细胞内和细胞外相互作用,已成为研究肿瘤机制、药物筛选和个性化癌症治疗的有力工具。球体、类器官和微流控装置等3D肿瘤模型技术正在成熟。共培养、3D生物打印和气液界面等新技术的应用进一步提高了模型的临床相关性。一些模型模拟了肿瘤微环境,有些甚至可以重建内源性免疫成分和微血管。近年来,一些学者将异种移植模型与类器官技术相结合,开发了匹配的/模型生物样本库,充分发挥了两种技术的优势,为某些肿瘤亚型中特定分子靶点的个体化精准治疗提供了理想的研究平台。到目前为止,上述技术已在结直肠癌研究领域得到广泛应用。我们的研究团队目前正在研究患者来源的肿瘤细胞样簇(一种自组装3D肿瘤模型)在指导结直肠癌术后化疗方案选择中的应用。在药物筛选实验中已取得了较高的建模成功率和满意的结果。毫无疑问,随着相关技术的进步,3D肿瘤模型将在结直肠癌的研究和临床实践中发挥越来越重要的作用。