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. Author manuscript; available in PMC: 2011 Dec 1.
Published in final edited form as: Oncogene. 2010 Aug 23;29(49):6418–6427. doi: 10.1038/onc.2010.373

Figure 5. High Taxol concentrations dramatically reduce tumour number and size in benign and invasive mouse models of intestinal cancer.

Figure 5

Cohorts of APCMIN/+ mice (45 days of age, n≥16) were treated every 2 weeks with either 10, 20mg/kg Taxol or vehicle until they reached 100 days of age. The most efficient treatment, 20mg/kg, was then increased to 3 injections a week every other week (Txl 20 x3). The same regime was used in an invasive model of tumourigenesis using Cre+ APCfl/+ PTEN fl/fl mice. Mice started treatment 2 weeks after induction and were sacrificed at 60 days post-induction. (a) Tumour number is not decreased in APCMIN/+ mice treated with Taxol 10mg/kg once every 2 weeks (p=0.48). (b) Taxol 20mg/kg treatment (once every 2 weeks) reduces significantly the number of tumours in APCMIN/+ (p=0.0007). (c) Taxol 20mg/kg administered 3 times a week every 2 weeks further reduces the number of tumours in APCMIN/+ (p=0.0001). (d) All Taxol regimes reduce the average tumour size in APCMIN/+ mice. Vehicle versus 10/mg/kg p=0.015, vehicle versus 20mg/kg p≤0.006. (e) Taxol reduces tumour number in Cre+ APCfl/+ PTEN fl/fl mice, p=0.001.