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©The Author(s) 2022.
World J Gastroenterol. Aug 28, 2022; 28(32): 4620-4634
Published online Aug 28, 2022. doi: 10.3748/wjg.v28.i32.4620
Published online Aug 28, 2022. doi: 10.3748/wjg.v28.i32.4620
Figure 4 Tumour growth curve of Panc-1 cells in subcutaneous pancreatic tumour growth in nude mice and tumour weight.
Treatments were given when the tumours reached 100 mm3. A: Untreated; B: Gemcitabine (10 mg/kg per 3 d); C: C5EOSEW5050ESA (200 mg/kg per day); D: C5EOSEW5050ESA (200 mg/kg per day) and gemcitabine (10 mg/kg per 3 d) combination; E: C5EOSEW5050ESA (400 mg/kg per day); F: C5EOSEW5050ESA (400 mg/kg per day) and gemcitabine (10 mg/kg per 3 d) combination. Combination treatment of 400 mg/kg C5EOSEW5050ESA and gemcitabine (F) synergistically reduced the tumour growth compared to a single treatment. The combination treatment of 400 mg/kg C5EOSEW5050ESA and gemcitabine (F) significantly reduced tumour weight compared to a single treatment. Error bars represent standard deviations. Statistics analysis (aP < 0.05; bP < 0.01; cP < 0.001, two-way ANOVA for tumour growth, one-way ANOVA with Tukey’s HSD posthoc test for tumour weight, n = 6 animals per group) using SPSS and GraphPad Prism 6.0 software.
- Citation: Yehya AHS, Subramaniam AV, Asif M, Kaur G, Abdul Majid AMS, Oon CE. Anti-tumour activity and toxicological studies of combination treatment of Orthosiphon stamineus and gemcitabine on pancreatic xenograft model. World J Gastroenterol 2022; 28(32): 4620-4634
- URL: https://www.wjgnet.com/1007-9327/full/v28/i32/4620.htm
- DOI: https://dx.doi.org/10.3748/wjg.v28.i32.4620