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. 2020 Nov 17;16(11):e1009117. doi: 10.1371/journal.pgen.1009117

Fig 3. Blocking DHODH with brequinar reduced reduces glioblastoma tumor xenografts growth in vivo.

Fig 3

(A) Representation of the subcutaneous xenograft experiment using LN229 cells. Mice were treated with 10 mg/kg brequinar with daily intraperitoneal injections (IP). (B) Tumor volume measurements of LN229 xenografts once the tumors reached 100 mm3. (C) Tumor weight of LN229 xenografts at day 60 (end of experiment). See also Supplementary S5B and S5C Fig. (D) Representative xenograft tumors from control and brequinar-treated mice. See also Supplementary S5B Fig. (E) Mouse weights at day 60 before the tumors were harvested. (F) Three representative control and brequinar-treated LN229 xenografts tumors showing increased blood vascularity in the control group (left panel) and qPCR for VEGFA in the LN229 xenografts. (G) Western blot of 5 control and brequinar-treated LN229 xenograft tumors for DHODH, p53, acetyl-tubulin, and HIF1α. * indicates p-values ≦ 0.05. Numerical values for each of the experiments represented are available in S3 Data.