The Donnelly Centre, University of Toronto, Toronto, 160 College St, Ontario, M5S 3E1, Canada.
Department of Chemical Engineering and Applied Chemistry, University of Toronto, 200 College Street, Toronto, Ontario, M5S 3E5, Canada.
Adv Mater. 2019 Sep;31(36):e1901166. doi: 10.1002/adma.201901166. Epub 2019 Jul 19.
Many 3D in vitro models induce breast cancer spheroid formation; however, this alone does not recapitulate the complex in vivo phenotype. To effectively screen therapeutics, it is urgently needed to validate in vitro cancer spheroid models against the gold standard of xenografts. A new oxime-crosslinked hyaluronan (HA) hydrogel is designed, manipulating gelation rate and mechanical properties to grow breast cancer spheroids in 3D. This HA-oxime breast cancer model maintains the gene expression profile most similar to that of tumor xenografts based on a pan-cancer gene expression profile (comprising 730 genes) of three different human breast cancer subtypes compared to Matrigel or conventional 2D culture. Differences in gene expression between breast cancer cultures in HA-oxime versus Matrigel or 2D are confirmed for 12 canonical pathways by gene set variation analysis. Importantly, drug response is dependent on the culture method. Breast cancer cells respond better to the Rac inhibitor (EHT-1864) and the PI3K inhibitor (AZD6482) when cultured in HA-oxime versus Matrigel. This study demonstrates the superiority of an HA-based hydrogel as a platform for in vitro breast cancer culture of both primary, patient-derived cells and cell lines, and provides a hydrogel culture model that closely matches that in vivo.
许多 3D 体外模型可诱导乳腺癌球体形成;然而,这本身并不能再现复杂的体内表型。为了有效地筛选治疗方法,迫切需要将体外癌症球体模型与异种移植物的金标准进行验证。设计了一种新的肟交联透明质酸(HA)水凝胶,通过控制凝胶化速率和机械性能来在 3D 中生长乳腺癌球体。与 Matrigel 或传统的 2D 培养相比,基于三种不同人类乳腺癌亚型的泛癌基因表达谱(包含 730 个基因),这种 HA-肟乳腺癌模型保持与肿瘤异种移植物最相似的基因表达谱。通过基因集变异分析,对 HA-肟与 Matrigel 或 2D 中乳腺癌培养物之间的 12 条经典途径的基因表达差异进行了确认。重要的是,药物反应取决于培养方法。与在 Matrigel 中培养相比,当在 HA-肟中培养时,乳腺癌细胞对 Rac 抑制剂(EHT-1864)和 PI3K 抑制剂(AZD6482)的反应更好。这项研究证明了基于 HA 的水凝胶作为体外乳腺癌培养的平台的优越性,无论是原代、患者来源的细胞还是细胞系,并且提供了一种与体内非常匹配的水凝胶培养模型。