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. 2013 Mar;344(3):589–599. doi: 10.1124/jpet.112.199646

Fig. 7.

Fig. 7.

(A) DB16, DB21, and 6DBF7 were tested in the LS174T lung cancer mouse model. As with the B16F10 model, tumors were allowed to grow to approximately 50 mm3. Treatment was initiated on day 8 by i.p. injection twice daily for a total dose of 10 mg/kg/day for 7 days. A control group of animals was treated with PBS alone. (B) As a preliminary assessment of pharmacodynamics in mice, we used the slower-growing MA148 tumor model, in which tumors grew to about 70 mm3 in 35 days. Treatment was then initiated with DB21 in four groups of animals (n = 10 each): control; two injections on days 35 and 42; three injections on days 35, 40, and 45; and five injections on day 35, 38, 41, 44, and 47. Tumor volumes in (A) and (B) are plotted as cubic millimeters versus days postinoculation (for all groups n = 11, ±S.E.M.). Tumor volumes were determined by measuring diameters of tumors using calipers, and the equation for the volume of a spheroid, (a2 × b × Π) / 6, where “a” is the width and “b” the length of the tumor. Tumor weights correlated well with tumor volumes calculated in this way.