Results
Orthotopic Colorectal Cancer Model: B-Tg(Luc) HCT 116 in B-NDG Mice
Establishment of orthotopic colorectal cancer model.
The B-NDG mice were inoculated with a volume of 40 μL of B-Tg(Luc) HCT 116 cell suspension (1×105, 5×105, 1×106), and the body weight and tumor fluorescence signal of the mice were recorded weekly. The results showed that the fluorescence signal gradually increased and body weight of mice had modest weight loss over time. This indicated that the cell line was successfully constructed as an orthotopic tumor model.
Orthotopic Colorectal Cancer Model: B-luc CT26.WT in Balb/c Mice
Establishment of orthotopic colorectal cancer model.
The B-NDG mice (F, n=6) were inoculated with B-Luc CT26.WT cell suspension. Subcutaneous tumor formation of B-Luc CT26.WT is slower than that of wild-type cells. and the body weight and tumor fluorescence signal of the mice were recorded weekly. The results showed that the fluorescence signal gradually increased and body weight of mice had modest weight loss over time. This indicated that the cell line was successfully constructed as an orthotopic tumor model.
Orthotopic Colorectal Cancer Model: B-luc-GFP HT-29 in B-NDG Mice
Establishment of orthotopic colorectal cancer model.
The colon of B-NDG mice were inoculated with B-luc-GFP HT-29 cell suspension, and the body weight and tumor fluorescence signal of the mice were recorded weekly. The results showed that the fluorescence signal gradually increased and body weight of mice had modest weight loss over time. This indicates that the cell line was successfully constructed as an orthotopic tumor model. This indicates that the cell line was successfully constructed as an orthotopic tumor model.
| Study ID: |
Groups |
Animal number |
Treatment |
Dosage (mg/kg) |
Lot No. |
Dosing Volume |
Dosing Route |
Treatment Schedule |
Treatment Times |
| 24P071529 |
G1 |
6 |
PBS |
- |
2933643 |
10μL/g |
i.v. |
QW |
2 |
| G2 |
6 |
DS-8201 |
3 |
394042 |
10μL/g |
i.v. |
QW |
2 |
| G3 |
6 |
DS-8201 |
6 |
394042 |
10μL/g |
i.v. |
QW |
2 |
Antitumor activity of anti-HER2 antibody in B-luc-GFP HT-29 colorectal orthotopic model.The DS-8201 significantly inhibited B-luc-GFP HT-29 tumor growth in B-NDG mice. B-luc-GFP HT-29 cells (5×10⁴) suspension mixed in Matrigel solution (1:1) was orthotopically implanted into B-NDG mice (female, 7 week-old, n=6). Mice were grouped when Imaging signal value reached approximately 2×10⁸ p/sec, at which time they were treated with the DS-8201 with different doses and schedules indicated in panel (A) Body weight during treatment. As shown in panel B, this drug was efficacious but mild, demonstrating that B-luc-GFP HT-29 colorectal orthotopic model could provide a powerful preclinical model for in vivo evaluation of DS-8201. Values are expressed as mean ± SEM. *p<0.05, ***p<0.01, ****p<0.001.
Orthotopic Colorectal Cancer Model: B-Tg(Luc) RKO in B-NDG Mice
Establishment of orthotopic colorectal cancer model
Establishment of orthotopic colorectal cancer model.
The colon of B-NDG mice were inoculated with B-Tg(Luc) RKO cell suspension (5×105, 1×106), and the body weight and tumor fluorescence signal of the mice were recorded weekly. The results showed that the fluorescence signal gradually increased and body weight of mice had modest weight loss over time. This indicates that the cell line was successfully constructed as an orthotopic tumor model. H&E staining showed that tumors metastasized in the liver, small intestine and pancreas.
Evaluation of the efficacy of orthotopic colorectal cancer model
| Study ID: |
Groups |
Animal number |
Treatment |
Dosage (mg/kg) |
Lot No. |
Dosing Volume |
Dosing Route |
Treatment Schedule |
Treatment Times |
| 21P079536 |
G1 |
6 |
PBS |
- |
2393840 |
10μL/g |
i.p. |
QW |
2 |
| G2 |
6 |
BsADC |
1mpk |
P220217A01 |
10μL/g |
i.p. |
QW |
2 |
| G3 |
6 |
BsADC |
3mpk |
P220217A01 |
10μL/g |
i.p. |
QW |
2 |
Evaluation of the efficacy of orthotopic colorectal cancer model.
The mice were randomly divided into PBS and BsADC groups after tumor inoculation based on imaging values. The body weight and tumor fluorescence signal of the mice were recorded weekly. BsADC significantly inhibited the growth of B-Tg(Luc) RKO orthotopic colorectal cancer, and the survival of the mice was significantly longer, demonstrating that this model can be well used for preclinical evaluation.
Orthotopic Colorectal Cancer Model: B-CMV-Luc LOVO#3-F03 + B-NDG mice (orthotopic)
| Study ID: |
Groups |
Animal strain |
Sex |
Cell line |
The amount of cells Inoculated |
The Volume of cells |
Animal number |
Remarks |
| 24P071544 |
G1 |
B-NDG mice |
F |
B-CMV-Luc LOVO |
1×106 |
0.04ml/mice |
6 |
Orthotopic, Cells mixed with Matrigel;1:1 |
| G2 |
B-NDG mice |
F |
B-CMV-Luc LOVO |
2×106 |
0.04ml/mice |
6 |
Orthotopic, Cells mixed with Matrigel;1:1 |
| G3 |
B-NDG mice |
F |
B-CMV-Luc LOVO |
5×106 |
0.1ml/mice |
6 |
Subcutaneously on the right flank Cells mixed with Matrigel;1:1 |
Establishment of orthotopic colorectal cancer model.
The B-NDG mice (F, n=6) were inoculated with B-CMV-Luc LOVO cell suspension (1×10⁶, 2×10⁶, 5×10⁶). And the body weight and tumor fluorescence signal of the mice were recorded weekly. The results showed that the fluorescence signal gradually increased. This indicates that the cell line was successfully constructed as an orthotopic tumor model.