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新型表型荧光三维共培养平台,可重现体内肿瘤进展并用于个体化治疗。

Novel Phenotypic Fluorescent Three-Dimensional Co-Culture Platforms for Recapitulating Tumor in vivo Progression and for Personalized Therapy.

机构信息

1. Advanced Personalized Diagnostics, 6006 Bangor Drive, Alexandria, VA 22303, USA.

出版信息

J Cancer. 2013 Dec 1;4(9):755-63. doi: 10.7150/jca.7813. eCollection 2013.

Abstract

Because three-dimensional (3D) in vitro models are more accurate than 2D cell culture models and faster and cheaper than animal models, they have become a prospective trend in the biomedical and pharmaceutical fields, especially for personalized and targeted therapies. Because appropriate 3D models can be customized to mimic the in vivo microenvironment wherein various cell populations grow within an intricate but well organized extracellular matrix (ECM), they can accurately recapitulate physiological and pathophysiological progressions. The majority of cancers are carcinomas, which originate from epithelial cells, and dynamically interact with non-malignant cells including stromal cells (fibroblasts), vascular cells (endothelial cells and pericytes), immune cells (macrophages and mast cells), and the ECM. Employing a tumor monoclonal colony, tumor xenograft or patient cancer biopsy into an in vivo-like microenvironment, the native signaling pathways, cell-cell and cell-matrix interactions, and cell phenotypes are preserved and our fluorescent phenotypic 3D co-culture platforms can then accurately recapitulate the tumor in vivo scenario including tumor induced angiogenesis, tumor growth, and metastasis. In this paper, we describe a robust and standardized method to co-culture a tumor colony or biopsy with different cell populations, e.g., endothelial cells, immune cells, pericytes, etc. The procedures for recovering cells from the co-culture for molecular analyses, imaging, and analyzing are also described. We selected ECM solubilized extract derived from Engelbreth-Holm-Swam sarcoma cells. Because the 3D co-culture platforms can provide drug chemosensitivity data within 9 days that is equivalent to the results generated from mouse tumor xenograft models in 50 days, the 3D co-culture platforms are more accurate, efficient, and cost-effective and may replace animal models in the near future to predict drug efficacy, personalize therapies, prevent drug resistance, and improve the quality of life.

摘要

由于三维(3D)体外模型比 2D 细胞培养模型更准确,比动物模型更快、更便宜,因此它们已成为生物医学和制药领域的一个有前途的趋势,特别是对于个性化和靶向治疗。由于适当的 3D 模型可以定制以模拟体内微环境,其中各种细胞群体在复杂但组织良好的细胞外基质(ECM)中生长,因此它们可以准确地再现生理和病理生理进展。大多数癌症是起源于上皮细胞的癌,它们与包括基质细胞(成纤维细胞)、血管细胞(内皮细胞和周细胞)、免疫细胞(巨噬细胞和肥大细胞)和 ECM 在内的非恶性细胞动态相互作用。将肿瘤单细胞克隆、肿瘤异种移植物或患者癌症活检置于类似于体内的微环境中,可以保留天然信号通路、细胞-细胞和细胞-基质相互作用以及细胞表型,然后我们的荧光表型 3D 共培养平台可以准确地再现包括肿瘤诱导血管生成、肿瘤生长和转移在内的体内肿瘤情况。在本文中,我们描述了一种稳健且标准化的方法,用于将肿瘤克隆或活检与不同的细胞群体(例如内皮细胞、免疫细胞、周细胞等)共培养。还描述了从共培养中回收细胞进行分子分析、成像和分析的程序。我们选择了从 Engelbreth-Holm-Swam 肉瘤细胞中提取的 ECM 溶解提取物。由于 3D 共培养平台可以在 9 天内提供相当于 50 天内从小鼠肿瘤异种移植模型获得的药物药敏数据,因此 3D 共培养平台更准确、高效、具有成本效益,并且可能在不久的将来取代动物模型,以预测药物疗效、个性化治疗、预防耐药性和提高生活质量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e4d/3842444/737f1159b30a/jcav04p0755g007.jpg

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