首页> 外文期刊>Journal of Cancer >Novel Phenotypic Fluorescent Three-Dimensional Co-Culture Platforms for Recapitulating Tumor in vivo Progression and for Personalized Therapy
【24h】

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

机译:新型表型荧光三维共培养平台,用于概括肿瘤在体内的进展并进行个性化治疗

获取原文
       

摘要

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.
机译:由于三维(3D)体外模型比2D细胞培养模型更精确,并且比动物模型更快且更便宜,因此它们已成为生物医学和制药领域的一种前瞻性趋势,尤其是针对个性化和靶向疗法。因为可以定制合适的3D模型来模拟体内微环境,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,所以它们可以准确地概括生理和病理生理学进程。大多数癌症是癌,其起源于上皮细胞,并与非恶性细胞动态相互作用,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)以及ECM。将肿瘤单克隆,肿瘤异种移植或患者癌症活检应用于体内类似的微环境中,天然的信号传导途径,细胞-细胞和细胞-基质相互作用以及细胞表型得以保留,然后我们的荧光表型3D共培养平台可以准确地概括了体内肿瘤的情况,包括肿瘤诱导的血管生成,肿瘤生长和转移。在本文中,我们描述了一种强大且标准化的方法,可与不同细胞群(例如内皮细胞,免疫细胞,周细胞等)共培养肿瘤集落或活检组织。从共培养物中回收细胞的步骤用于分子分析,还介绍了成像和分析。我们选择了来自Engelbreth-Holm-Swam肉瘤细胞的ECM增溶提取物。由于3D共培养平台可以在9天之内提供药物化学敏感性数据,相当于50天小鼠肿瘤异种移植模型产生的结果,因此3D共培养平台更准确,有效且具有成本效益,可以替代动物模型可在不久的将来预测药物疗效,个性化疗法,预防耐药性并改善生活质量。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号