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. 2018 May 4;9(34):23462–23481. doi: 10.18632/oncotarget.25231

Table 2. Effect of SAR100842 on ovarian cancer metastasis incidence in two model systemsa.

Site: Lesion Depth, where applicable: Fraction of mice with metastasesb:
SKOV3 Model System: OVCAR5 Model System:
Vehicle: SAR100842:
Day 2 pi
SAR100842:
Day 10 pi
Vehicle: SAR100842:
Day 2 pi
SAR100842:
Day 10 pi
Omentum 13/13 10/10 10/10 9/12 8/10 7/10
Liver Surface 11/13 9/10 9/10 9/12 9/10 6/10
Invasive 1/13 0/10 0/10 2/12 2/10 1/10
Diaphragm Surface 12/13 7/10 10/10 7/12 5/10 4/10
Invasive 12/13 7/10 10/10 7/12 5/10 2/10
Lymph Node Surface 4/13 2/10 3/10 0/12 1/10 3/10
Invasive 0/13 0/10 0/10 0/12 0/10 0/10
Kidney Surface 5/13 1/10 2/10 0/12 0/10 0/10
Invasive 0/13 0/10 0/10 0/12 0/10 0/10
Pancreas Surface 0/13 0/10 0/10 7/12 8/10 6/10
Invasive 0/13 0/10 0/10 5/12 5/10 4/10
Peritoneal Surface 13/13 10/10 10/10 11/12 9/10 7/10
Invasive 0/13 0/10 0/10 0/12 0/10 0/10
Ascites 0/13 0/10 0/10 3/12 1/10 1/10

aMice were injected intraperitoneally with either SKVO3 or OVCAR5 and treated with either vehicle or 30 mg/kg SAR100842 twice daily starting on either day 2 or day 10 post cell injection (pi). At endpoint, all organs thought to harbor tumor were fixed in 10% NBF before embedding in paraffin for sectioning and H&E staining.

bMetastases were quantified in three sections every 200 μm through each tissue, and characterized as being on the surface of the tissue or invading into the tissue, in consultation with a pathologist.