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. 2018 Apr 19;3(8):e99263. doi: 10.1172/jci.insight.99263

Figure 1. Specific targeting of iExosomes for human PDAC cells with KrasG12D.

Figure 1

(A) Volcano plots depicting log2 fold change (red, upregulated genes; blue, downregulated genes; gray, genes that were not significantly deregulated) and –log10 (P value) of differentially expressed genes between siKrasG12D–1 iExo–treated Panc-1 cells and all controls and BxPC-3 cells. (B) Tumor volume measured by MRI of siKrasG12D–1 iExo (n = 7) or siScrbl iExo (n = 7) at baseline (day 0 = day 62 after tumor induction) and after treatment (day 30, 81, and 228 posttreatment start [PTS]). #, no measurement available; mice died. (C) Representative MRI images of PDX pancreas tumors; a yellow dashed line encircles the tumors. (D) Kaplan-Meier curve indicating the survival of PDX mice in the listed treatment groups after birth (siKrasG12D–1 iExo [n = 7], siScrbl iExo [n = 7]; log-rank (Mantel-Cox) test). The approximated time for the natural life span of nude mice is indicated by the red dotted line. (E) Tumor weight at end point in studies with PDX mice (siKrasG12D iExo [n = 7], siScrbl iExo [n = 7]). (F) Representative H&E image of aggressively invasive pancreatic tumors in siScrbl iExo–treated mice, in comparison with predominant inflammation and markedly reduced tumors in pancreata of siKrasG12D–1 iExo–treated mice. Scale bars: 100 μm (left); 50 μm (right). The data are presented as the mean ± SEM. Unless otherwise stated, unpaired 2-tailed t test was used to determine statistical significance. *P < 0.05, ** P < 0.01. See Supplemental Source Data 1 and 2.

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