fig7

Novel <i>N</i>-chloroacetyl-2-pyrazoline analogs with 2-naphthyl and ferrocenyl groups: targeting histamine receptor H1 to overcome colorectal cancer drug resistance

Figure 7. Clac10 (5c) and Clac12 (5e) reduce the growth of colon cancer xenografts in NSG mice. (A) HCT116 cells were injected into both flanks of NSG mice (n = 5), and tumors (n = 10; each mouse carrying 2 xenograft tumors, totaling 10 tumors per group) were allowed to develop until palpable. Then, Clac10 and Clac12 (20 mg/kg body weight) were injected intraperitoneally daily for 24 days; At the end of the study, the tumors were removed, imaged (B), and analyzed further; (C) The tumors in Clac10-treated mice were smaller than those in the control group; (D) Treatment with Clac10 and Clac12 resulted in significantly lower tumor volumes than in the control group. Tumor volume was measured weekly. The data are shown as mean ± SEM. We used ordinary one-way ANOVA for statistical comparisons. *P < 0.05, **P < 0.01, ***P < 0.001. SEM: Standard error of the mean; ANOVA: analysis of variance.

Cancer Drug Resistance
ISSN 2578-532X (Online)

Portico

All published articles will preserved here permanently:

https://www.portico.org/publishers/oae/

Portico

All published articles will preserved here permanently:

https://www.portico.org/publishers/oae/