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International Journal of Bioprinting                                     Bioprinting of a multicellular model



                         A                                   D













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                         C                                    F














            Figure 12. Dose response curve of 5-FU (A), oxaliplatin (B), and irinotecan (C) between 2D culture group and 3D Printing-S group after 72 h of treatment.
            IC  represents median inhibitory concentration. Dose-effect curves of 5-FU (D), oxaliplatin (E), and irinotecan (F) in the 3D printing-M after 72 h of
             50
            treatment.

            well in the 3D printing-M and that the constructed 3D   3D printing-S group. GO enrichment analysis indicated
            printing-M of mesenchymal tumor cells was successful.   that compared with colorectal cancer cells cultured in
            In addition, through exploration and attempts, we were   2D culture, the gene expression of colorectal cancer
            able to produce frozen tissue sections of 3D bioprinted   cells cultured in a 3D bioprinted model was significantly
            models and understand the morphological characteristics   different in biological processes, cell composition, and
                                                                              [39]
            of tumor cells and interstitial cells through HE staining of   molecular function . KEGG enrichment analysis showed
            the frozen sections. The results show that the cell lines have   that compared with the 2D culture group, metabolic
            a certain degree of tissue characteristics depending on the   pathway, and oxidative phosphorylation pathway were the
            bionic characteristics of the 3D bioprinting technology.  most significantly upregulated gene enrichment pathways
                                                               in the 3D printing-S group [40-42] . These results suggest
              From the perspective of transcriptome, we analyzed the   that colorectal cancer cells in the 3D bioprinted model
            differences in gene expression among the 3D printing-S   are significantly different from those in the 2D cultures.
            group, 2D culture group, sandwich culture group, and 3D   The main sources of these differences are the different
            printing-M group. As can be seen from the volcano map of   cell culture models, the different structures of the cell
            DEGs, the number of DEGs in SW480 cells was as high as   survival space, and the different degrees of communication
            11107 between the two culture models of 2D culture and   between cells. The functions of the hub genes between the


            Volume 9 Issue 3 (2023)                        393                         https://doi.org/10.18063/ijb.694
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