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Fig. 13 | Journal of Translational Medicine

Fig. 13

From: Immunotherapy landscape analyses of necroptosis characteristics for breast cancer patients

Fig. 13

The silence of IPMK enhanced the expression of immune checkpoint and promoted infiltration and M2 polarization of macrophages. The relative expression levels of PD-1, PD-L1, and CTLA-4 in MCF-7 (A) and MDA-MB-231 cells (B) after silencing IPMK were compared with the si-NC groups. After co-culturing THP-1 generated M0 macrophages with BC cells (C) for 48 h with Transwell plates, the expressions of M2 biomarkers (ARG1 and CD23) and M1 biomarkers (INOS and CCR27) of macrophage (D–G) were detected by qRT-PCR. Then, the macrophages were seeded in the upper chamber of Transwell plates (H). The number of migrated macrophages after co-culture for 48 h with MCF-7 (I) and MDA-MB-231 (J) were calculated by Image J. The protein expressions of IL-4 and IL-6 of MCF-7 (K) and MDA-MB-231 cells (L) were detected using western blot analysis. *P < 0.5; **P < 0.01; ***P < 0.001.

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