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. Author manuscript; available in PMC: 2020 May 1.
Published in final edited form as: Cancer Res. 2019 Sep 13;79(21):5626–5639. doi: 10.1158/0008-5472.CAN-19-0800

Figure 2. Tumor growth is reduced in neutrophil extracellular traps (NETs) depleted mice.

Figure 2.

Subcutaneous tumors using MC38 cells (1×106) injected subcutaneously (A) or through the spleen (C) for the metastasis model showing smaller tumors harvested 3 weeks post-inoculation in PAD4 KO compared to WT mice (n=5/group). B and D, Graphs showing significantly decreased tumor volume and surface liver nodules, respectively, in PAD4 KO mice compared to WT control *P <0.05. E, Hematoxylin and Eosin (H&E) staining of liver sections exhibit decreased tumor burden in PAD4 KO mice (n=5) compared to WT **P <0.01. F, Similarly, mice treated daily with DNAse (50ug) or Neutrophil Elastase inhibitor (NEi) (2.0 mg/kg) in both subcutaneous (n=5) and metastatic model (n=4) showed decrease tumor growth compared to controls. G, Graph representing tumor growth curve in DNAse (50ug) treated Nu/Nu athymic mice inoculated with HCT116 and Huh7 cell lines (1×106) (n=5/group). Data presented as mean SEM. *P <0.05.