4.7 Article

Engineering a Vascularized 3D Hybrid System to Model Tumor-Stroma Interactions in Breast Cancer

Journal

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fbioe.2021.647031

Keywords

hydrogel; alginate; vascularized stroma; outgrowth endothelial cells; angiogenesis; tissue engineering; organoid

Funding

  1. FEDER - Fundo Europeu de Desenvolvimento Regional funds through the COMPETE 2020 - Operational Programme Competitiveness and Internationalization (POCI), Portugal 2020
  2. Portuguese funds through FCT - Fundacao para a Ciencia e a Tecnologia/Ministerio da Ciencia, Tecnologia e Ensino Superior [POCI-01-0145-FEDER028744, PTDC/BTMMAT/28744/2017]
  3. FCT [DL 57/2016/CP1360/CT0006]
  4. IF research position [IF/00296/2015]
  5. Fundação para a Ciência e a Tecnologia [DL 57/2016/CP1360/CT0006] Funding Source: FCT

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The stromal microenvironment of breast tumors plays a crucial role in tumor development and metastasis, with tumor angiogenesis requiring cooperation between various cell types and extracellular matrix. The developed hybrid alginate-based 3D system allows for the simulation and support of epithelial morphogenesis and endothelial tubulogenesis in breast tumors.
The stromal microenvironment of breast tumors, namely the vasculature, has a key role in tumor development and metastatic spread. Tumor angiogenesis is a coordinated process, requiring the cooperation of cancer cells, stromal cells, such as fibroblasts and endothelial cells, secreted factors and the extracellular matrix (ECM). In vitro models capable of capturing such complex environment are still scarce, but are pivotal to improve success rates in drug development and screening. To address this challenge, we developed a hybrid alginate-based 3D system, combining hydrogel-embedded mammary epithelial cells (parenchymal compartment) with a porous scaffold co-seeded with fibroblasts and endothelial cells (vascularized stromal compartment). For the stromal compartment, we used porous alginate scaffolds produced by freeze-drying with particle leaching, a simple, low-cost and non-toxic approach that provided storable ready-to-use scaffolds fitting the wells of standard 96-well plates. Co-seeded endothelial cells and fibroblasts were able to adhere to the surface, spread and organize into tubular-like structures. For the parenchymal compartment, a designed alginate gel precursor solution load with mammary epithelial cells was added to the pores of pre-vascularized scaffolds, forming a hydrogel in situ by ionic crosslinking. The 3D hybrid system supports epithelial morphogenesis in organoids/tumoroids and endothelial tubulogenesis, allowing heterotypic cell-cell and cell-ECM interactions, while presenting excellent experimental tractability for whole-mount confocal microscopy, histology and mild cell recovery for down-stream analysis. It thus provides a unique 3D in vitro platform to dissect epithelial-stromal interactions and tumor angiogenesis, which may assist in the development of selective and more effective anticancer therapies.

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