Weigelt Britta, Bissell Mina J
Life Sciences Division, Lawrence Berkeley National Laboratory, 1 Cyclotron Road, MS 977-225A, Berkeley, CA 94720, USA.
Semin Cancer Biol. 2008 Oct;18(5):311-21. doi: 10.1016/j.semcancer.2008.03.013. Epub 2008 Mar 26.
The normal mammary gland and invasive breast tumors are both complex 'organs' composed of multiple cell types as well as extracellular matrix in three-dimensional (3D) space. Conventionally, both normal and malignant breast cells are studied in vitro as two-dimensional monolayers of epithelial cells, which results in the loss of structure and tissue function. Many laboratories are now investigating regulation of signaling function in the normal mammary gland using 3D cultures. However, it is also important to assay malignant breast cells ex vivo in a physiologically relevant environment to more closely mimic tumor architecture, signal transduction regulation and tumor behavior in vivo. Here we present the potential of these 3D models for drug testing, target validation and guidance of patient selection for clinical trials. We also argue that in order to get full insight into the biology of the normal and malignant breast, and to create in vivo-like models for therapeutic approaches in humans, we need to continue to create more complex heterotypic models to approach the full context the cells encounter in the human body.
正常乳腺和浸润性乳腺肿瘤都是复杂的“器官”,由多种细胞类型以及三维(3D)空间中的细胞外基质组成。传统上,正常和恶性乳腺细胞都作为上皮细胞的二维单层在体外进行研究,这导致了结构和组织功能的丧失。现在许多实验室正在使用3D培养来研究正常乳腺中信号功能的调节。然而,在生理相关环境中对恶性乳腺细胞进行体外分析也很重要,以便更紧密地模拟体内的肿瘤结构、信号转导调节和肿瘤行为。在这里,我们展示了这些3D模型在药物测试、靶点验证和临床试验患者选择指导方面的潜力。我们还认为,为了全面了解正常和恶性乳腺的生物学特性,并为人类治疗方法创建类似体内的模型,我们需要继续创建更复杂的异型模型,以接近细胞在人体中遇到的完整环境。