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. 2019 Aug 29;27(12):2091–2099. doi: 10.1016/j.ymthe.2019.08.012

Figure 4.

Figure 4

Systemic Administration of 18E7 gRNAs +WT Cas9 Packaged in Stealth Liposomes Effectively Eliminated HeLa Xenografts and Prolonged Survival

(A) HeLa cells were subcutaneously inoculated in Rag1 mice and allowed to grow to 50 mm3 before being treated with a total of 10 μg/dose of plasmid DNA coated in stealth liposomes (18E7 sgRNA+ WT Cas9 plasmids [treatment], nonspecific gRNA + WT Cas9 [control], or PBS [untreated]). Tumor volume was monitored for 46 days (experiment endpoint, tumor size = 1,000 mm3). The arrows represent the days of treatment injection. The legend illustrates whether 18E7 or control treatments were injected to treatment arms (#1 and #2). Data are presented as mean ± SD. (B) The survival analysis of established HeLa xenografts in Rag1 mice after 18E7 targeted treatment, control (nonspecific gRNA + WT Cas9), or untreated (PBS only) in days. (C) The apoptotic cell count in anti-caspase-3-stained tumor tissues in 18E7, control, and untreated tumor sections. (D) Immunohistochemical staining of tumor tissues with H&E or anti-cleaved caspase-3 antibody in 18E7 or control treated tumor specimens. (E) Immunohistochemical staining of tumor tissues after seven doses of treatment (treatment #2 group) with 18E7 sgRNA + WT Cas9, with H&E or p16 antibody. Statistical significance was assessed by ANOVA with post hoc analysis. *p < 0.05, **p < 0.01, ***p < 0.001.