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. Author manuscript; available in PMC: 2021 Mar 3.
Published in final edited form as: Lab Chip. 2020 Mar 3;20(5):873–888. doi: 10.1039/c9lc00550a

Figure.2.

Figure.2

Tumor-on-a-chip models to induce chemotaxis and study cell-cell crosstalk. A. A V-shape double-channel microfluidic device for chemotaxis. Inlet 1 was designed for media flow and inlet 2 for chemokine perfusion. (reproduced with permission from ref. 32) B. Microfluidic channel design for single-cell chemotaxis. Chemical gradients were generated from the right channel to the left channel. (reproduced with permission from ref. 36) C. Parallel-channels in a 3D collagen scaffold to induce a response of endothelial cells in an angiogenic factors gradient. (reproduced with permission from ref. 39) D. Tumor spheroids and CAFs co-cultured in a 3D hydrogel-based microfluidic chip, separated with medium channels. (reproduced with permission from ref. 46) E. A metastasis-on-a-chip model with a gut organoid and a liver organoid located in two connected PDMS chambers. (reproduced with permission from ref. 50)