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肿瘤学研究中的三维体外培养模型

Three-dimensional in vitro culture models in oncology research.

作者信息

Jubelin Camille, Muñoz-Garcia Javier, Griscom Laurent, Cochonneau Denis, Ollivier Emilie, Heymann Marie-Françoise, Vallette François M, Oliver Lisa, Heymann Dominique

机构信息

Nantes Université, CNRS, US2B, UMR 6286, 44000, Nantes, France.

Institut de Cancérologie de l'Ouest, Tumor Heterogeneity and Precision Medicine Lab.. Université de Nantes, 44805, Saint-Herblain, France.

出版信息

Cell Biosci. 2022 Sep 11;12(1):155. doi: 10.1186/s13578-022-00887-3.

Abstract

Cancer is a multifactorial disease that is responsible for 10 million deaths per year. The intra- and inter-heterogeneity of malignant tumors make it difficult to develop single targeted approaches. Similarly, their diversity requires various models to investigate the mechanisms involved in cancer initiation, progression, drug resistance and recurrence. Of the in vitro cell-based models, monolayer adherent (also known as 2D culture) cell cultures have been used for the longest time. However, it appears that they are often less appropriate than the three-dimensional (3D) cell culture approach for mimicking the biological behavior of tumor cells, in particular the mechanisms leading to therapeutic escape and drug resistance. Multicellular tumor spheroids are widely used to study cancers in 3D, and can be generated by a multiplicity of techniques, such as liquid-based and scaffold-based 3D cultures, microfluidics and bioprinting. Organoids are more complex 3D models than multicellular tumor spheroids because they are generated from stem cells isolated from patients and are considered as powerful tools to reproduce the disease development in vitro. The present review provides an overview of the various 3D culture models that have been set up to study cancer development and drug response. The advantages of 3D models compared to 2D cell cultures, the limitations, and the fields of application of these models and their techniques of production are also discussed.

摘要

癌症是一种多因素疾病,每年导致1000万人死亡。恶性肿瘤的内部和之间的异质性使得难以开发单一的靶向方法。同样,它们的多样性需要各种模型来研究癌症起始、进展、耐药性和复发所涉及的机制。在基于体外细胞的模型中,单层贴壁(也称为二维培养)细胞培养使用的时间最长。然而,对于模拟肿瘤细胞的生物学行为,特别是导致治疗逃逸和耐药性的机制,它们似乎往往不如三维(3D)细胞培养方法合适。多细胞肿瘤球体被广泛用于三维研究癌症,并且可以通过多种技术生成,例如基于液体和基于支架的三维培养、微流控和生物打印。类器官是比多细胞肿瘤球体更复杂的三维模型,因为它们是由从患者分离的干细胞产生的,并且被认为是在体外重现疾病发展的强大工具。本综述概述了为研究癌症发展和药物反应而建立的各种三维培养模型。还讨论了三维模型与二维细胞培养相比的优势、局限性以及这些模型及其生产技术的应用领域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9549/9465969/aae2a93a53c3/13578_2022_887_Fig1_HTML.jpg

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