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Image Search Results
Journal: Scientific Reports
Article Title: The IAP Antagonist SM-164 Eliminates Triple-Negative Breast Cancer Metastasis to Bone and Lung in Mice
doi: 10.1038/s41598-020-64018-z
Figure Lengend Snippet: SM-164 induces apoptosis of breast cancer cells in combination with TNFα released by tumor-associated macrophages. ( A ) The parental MDA-MB-231 cells were treated with vehicle, TNFα (1 ng/ml) or TNFα + the indicated doses of SM-164 or BV6 overnight. Annexin V + PI +/− apoptotic cells were analyzed by flow cytometry. ( B ) Parental MDA-MB-231 cells were treated with the indicated doses of SM-164, BV6 or AT-406 alone, or with a combination of them plus TNFα (1 ng/ml) for 8 hours. Cell lysates were used to test protein levels of cIAP1/cIAP2 and GAPDH. ( C ) 1 × 10 4 GFP + MDA-MB-231 cells were cultured alone or together with WT mouse BM cells in the presence of M-CSF +/− PBS (P) or IL-4 for 3 d, during which 3 nM SM-164 and 1 μg/ml TNFR:Fc (R:Fc) were added for the last 16 hr (last group on right +R:Fc). Annexin V + PI +/− apoptotic cells in the GFP + population were analyzed by flow cytometry (left panel). The total number of GFP + cells (left graph) was calculated based on % of GFP + cells in the total cell number, and % of Annexin V + PI +/− apoptotic cells in the GFP + population (right graph) was calculated. *p < 0.05 and **p < 0.01, one-way ANOVA +/Dunnett test.
Article Snippet: MDA-MB-231 cells were treated with different doses of SM-164 +/− 1 ng/ml
Techniques: Flow Cytometry, Cell Culture
Journal: Scientific Reports
Article Title: The IAP Antagonist SM-164 Eliminates Triple-Negative Breast Cancer Metastasis to Bone and Lung in Mice
doi: 10.1038/s41598-020-64018-z
Figure Lengend Snippet: ADR-resistant (R) MDA-MB-231 cells are also resistant to SM-164, while SM-164-R MDA-MB-231 cells are sensitive to ADR. ( A ) Growth curve of the parental and ADR-R MDA-MB-231 cells, starting at 1 × 10 4 cells/well, in a well of 6-well-plates treated with 30 ng/ml ADR or vehicle, and passaged to 60- and 100-mm dishes, respectively, when untreated cells grew to sub-confluence. 3 wells/group, **p < 0.01, one-way ANOVA +/Dunnett test. ( B ) Parental and ADR-R MDA-MB-231cells were treated with the indicated doses of SM-164 plus 1 ng/ml of TNFα overnight. Annexin V + PI +/− apoptotic cells were analyzed by flow cytometry. ( C ) 0.5 × 10 4 parental and SM-R MDA-MB-231 cells in 60 mm dishes were cultured overnight followed by treatment with 1 ng/ml TNFα plus the indicated doses of SM-164 for 3 days, and surviving cells were counted. ( D ) The parental and SM-164-R cells (0.5 × 10 4 cells in 60 mm dishes) were treated with the indicated doses of ADR for 6 days and cell numbers were counted after digestion with 0.2% trypsin. **p < 0.01 vs. the respective parental cells, one-way ANOVA +/Dunnett test. The experiments were repeated 3 times with similar results.
Article Snippet: MDA-MB-231 cells were treated with different doses of SM-164 +/− 1 ng/ml
Techniques: Flow Cytometry, Cell Culture