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Jackson Laboratory nf2 men luc2
The brigatinib + INK128 combination effectively <t>shrank</t> <t>intracranial</t> <t>AG-NF2-Men-Luc2</t> meningioma xenografts. A, Mice with established meningioma xenografts were treated with vehicle, brigatinib, INK128, or the brigatinib + INK128 combination by oral gavage, and tumor growth was monitored by BLI. The relative tumor-emitted BL signals were quantified and denoted as % of total flux after treatment relative to the total flux prior to treatment designated as one (100%). B, To assess potential tumor regrowth, we stopped treating mice in the INK128 or combination treatment group for 8 weeks and continued monitoring tumor growth by BLI for another 6 weeks. To examine the effects of re-treatment, we resumed treatment and continued BLI monitoring for 6 more weeks. The data are shown as the mean ± SE.
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The brigatinib + INK128 combination effectively shrank intracranial AG-NF2-Men-Luc2 meningioma xenografts. A, Mice with established meningioma xenografts were treated with vehicle, brigatinib, INK128, or the brigatinib + INK128 combination by oral gavage, and tumor growth was monitored by BLI. The relative tumor-emitted BL signals were quantified and denoted as % of total flux after treatment relative to the total flux prior to treatment designated as one (100%). B, To assess potential tumor regrowth, we stopped treating mice in the INK128 or combination treatment group for 8 weeks and continued monitoring tumor growth by BLI for another 6 weeks. To examine the effects of re-treatment, we resumed treatment and continued BLI monitoring for 6 more weeks. The data are shown as the mean ± SE.

Journal: Cancer Research Communications

Article Title: Combining Brigatinib with mTOR Inhibition to Effectively Treat NF2-SWN–Associated and Sporadic NF2 -Deficient Meningiomas

doi: 10.1158/2767-9764.CRC-25-0563

Figure Lengend Snippet: The brigatinib + INK128 combination effectively shrank intracranial AG-NF2-Men-Luc2 meningioma xenografts. A, Mice with established meningioma xenografts were treated with vehicle, brigatinib, INK128, or the brigatinib + INK128 combination by oral gavage, and tumor growth was monitored by BLI. The relative tumor-emitted BL signals were quantified and denoted as % of total flux after treatment relative to the total flux prior to treatment designated as one (100%). B, To assess potential tumor regrowth, we stopped treating mice in the INK128 or combination treatment group for 8 weeks and continued monitoring tumor growth by BLI for another 6 weeks. To examine the effects of re-treatment, we resumed treatment and continued BLI monitoring for 6 more weeks. The data are shown as the mean ± SE.

Article Snippet: The clone expressing the highest luciferase activity, designated AG-NF2-Men-Luc2, was tested for its ability to establish xenografts by injecting 5 × 10 5 cells subcutaneously in the flank or stereotactically into the skull base of 8- to 12-week-old NSG mice (The Jackson Laboratory).

Techniques: