Details

Autor(en) / Beteiligte

• Sakai, Kosei
• Kato, Daiki
• Yoshinaka, Junka
• Takahashi, Yosuke
• Ikeda, Namiko
• Aoki, Susumu
• Iguchi, Takaaki
• Ishikawa, Shingo
• Yamagishi, Norio
• Shimamura, Shunsuke
• Nakagawa, Takayuki

Titel

Effects of trastuzumab emtansine on canine urothelial carcinoma cells in vitro and in vivo

Ist Teil von

• Veterinary & comparative oncology, 2024-06, Vol.22 (2), p.230-238

Ort / Verlag

Oxford, UK: Blackwell Publishing Ltd

Erscheinungsjahr

2024

Quelle

Alma/SFX Local Collection

Beschreibungen/Notizen

• Urothelial carcinoma (UC) is the most common malignancy of the urinary tract in dogs and has aggressive behaviour. Although human epidermal growth factor receptor 2 (HER2) is a known therapeutic target with evidence in canine UC, the efficacy of anti‐HER2 antibody drugs remains unknown. This study aimed to investigate the effects of anti‐HER2 antibody drugs including trastuzumab and trastuzumab emtansine (T‐DM1) on canine UC cell lines in vitro and in vivo. Four canine UC cell lines (Nene, TCCUB, Love, and Sora) were used. In western blotting, HER2 protein expression was observed in all the cell lines. Although both trastuzumab and T‐DM1 showed dose‐dependent growth inhibitory activity in the cell lines, T‐DM1 showed much stronger activity than that of trastuzumab. In flow cytometry analyses with the canine UC cell line (Sora), T‐DM1 but not trastuzumab significantly increased the percentages of early and late apoptotic cells in annexin V apoptotic assays and the sub‐G1 phase fraction in cell cycle analyses. For the in vivo experiment, the canine UC cells (Sora) were subcutaneously injected into nude mice. Four days after inoculation, trastuzumab, T‐DM1, or vehicle was administered intraperitoneally once a week for three times. Tumour volumes were significantly smaller in the T‐DM1 group compared to the trastuzumab and vehicle control groups. These findings indicate that T‐DM1 exerts a stronger antitumour effect than that of trastuzumab on canine UC cells in vitro and in vivo, possibly by inducing apoptosis due to DM1.