NCI-H1703 Subcutaneous Xenograft Tumor Mouse Model

MP Michael R. Paillasse
ME Michael Esquerré
FB Florie A. Bertrand
CP Céline Poussereau-Pomié
MP Mélanie Pichery
VV Virgile Visentin
GG Geneviève Gueguen-Dorbes
FG Florence Gaujarengues
PB Pauline Barron
GB Gaelle Badet
AB Anne Briaux
PA Pierre-Benoit Ancey
DS David Sibrac
EE Eric Erdociain
Dennis Özcelik
JM Jérôme Meneyrol
VM Valérie Martin
AG Anne Gomez-Brouchet
JS Janik Selves
PR Philippe Rochaix
MB Maxime Battistella
CL Céleste Lebbé
JD Jean-Pierre Delord
FD Frédérique Dol-Gleizes
FB Françoise Bono
IB Isabelle Blanc
AA Antoine Alam
IH Ian Hunneyball
MW Mark Whittaker
PF Pierre Fons
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A total number of 40 homozygous NOD.CB17 Prkdcscid/NCrHsd mice were used for the xenograft tumor model. On the day of implantation, NCI-H1703 cells were harvested and suspended at a concentration of 1 × 108 cells per mL in an equal mix of Cultrex:RPMI without supplements. A volume of 100 μL was injected into the right hind flank of each animal. Tumor volumes were monitored until mean tumor volume reached 150 mm3. Then, mice were stratified into four treatment groups of each 10 mice and orally dosed twice per day with either EVT801 30 mg/kg and EVT801 vehicle [Soluplus (BASF)/water/hydroxypropylcellulose SL (Nisso America)], or 30 mk/kg pazopanib and pazopanib vehicle (0.5% Hydroxypropyl methylcellulose trimellitate (HPMCT) + 0.1% Tween-80). A period of 8 hours was observed between the first and second daily dose.

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