Skip to main content
. 2020 Jul 24;15(7):e0219632. doi: 10.1371/journal.pone.0219632

Fig 4. DCH-paclitaxel reduces hGBM growth progression rates monitored by luciferase bioluminescence imaging in vivo and prolongs survival.

Fig 4

A. Schematic of the mouse brain identifying the anatomical location of the gliomasphere and then DCH injections within the caudate putamen (CP) region of the striatum. B and C. Graphs showing Luciferase Total Flux (p/s = photons/second) progression as a function of time as measured by bioluminescence IVIS imaging for each animal receiving either DCH only or DCH-paclitaxel in cohort 1 (n = 4 animals per group) (B) or cohort 2 (n = 10 animals per group) (C). An exponential growth regression was applied to each treatment group in B and C which is represented by a straight line on the semi-log plot. The delta t (Δt) is the time between the same absolute average flux value between the two treatment groups and was calculated to be approximately 1.5 weeks for cohort 2 D. Kaplan Meyer survival curve for cohort 2 animals which demonstrated that DHC-paclitaxel conferred a significant median survival time increase of 2.5 week (or a 23% extension of life) compared to the DCH alone (p = 0.0063). Statistic calculated by log rank test calculated by Prism 6 software. E. In a third cohort, animals were injected with gliomasphere cells followed by DHC two weeks later. The effect was smaller and the survival curve did not meet statistical significance.