Figure 5.
Concurrent Bcl-xL blockade outperforms venetoclax in the presence of stromal support. (A-B) Dose-response curves of S63845 in the presence or absence of stromal support: MSCT+ cells (A); HS-5 cells (B). (C) Dose-response curves of A-1210477 in the presence or absence of stromal support (MSCT+). (D) Efficacy studies of S63845 in MM cell monoculture, direct cell-cell contact coculture or Transwell coculture with MSCT+ or HS-5 stromal cells. (A-D) Graphs represent the mean ± standard deviation of 3 independent experiments performed in triplicate. *P < .05, **P < .01; ***P < .001. (E) Dose-response curves of S63845 in monoculture and coculture (MSCT+) in the presence or absence of the Bcl-xL inhibitor A-1331852 (100 nM) or the Bcl-2 inhibitor venetoclax (100 nM), respectively. Corresponding IC50 values are indicated. Dose-response curves represent the mean of 3 independent experiments performed in triplicate. (F) Primary CD138+ MM cells (n = 10) escape S63845 therapy in the presence of stromal support (MSCT+). This effect is overcome by the concurrent treatment with A-1331852 (complete rescue) or venetoclax (partial rescue). Viable cells were determined via annexin V/7 AAD staining 24 hours after treatment initiation. Graph shows median viability with interquartile range. *P < .05; **P < .01.

Concurrent Bcl-xL blockade outperforms venetoclax in the presence of stromal support. (A-B) Dose-response curves of S63845 in the presence or absence of stromal support: MSCT+ cells (A); HS-5 cells (B). (C) Dose-response curves of A-1210477 in the presence or absence of stromal support (MSCT+). (D) Efficacy studies of S63845 in MM cell monoculture, direct cell-cell contact coculture or Transwell coculture with MSCT+ or HS-5 stromal cells. (A-D) Graphs represent the mean ± standard deviation of 3 independent experiments performed in triplicate. *P < .05, **P < .01; ***P < .001. (E) Dose-response curves of S63845 in monoculture and coculture (MSCT+) in the presence or absence of the Bcl-xL inhibitor A-1331852 (100 nM) or the Bcl-2 inhibitor venetoclax (100 nM), respectively. Corresponding IC50 values are indicated. Dose-response curves represent the mean of 3 independent experiments performed in triplicate. (F) Primary CD138+ MM cells (n = 10) escape S63845 therapy in the presence of stromal support (MSCT+). This effect is overcome by the concurrent treatment with A-1331852 (complete rescue) or venetoclax (partial rescue). Viable cells were determined via annexin V/7 AAD staining 24 hours after treatment initiation. Graph shows median viability with interquartile range. *P < .05; **P < .01.

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