Oh Sungryong, Choi Kiheon, Kim Kyoung Mee, Jung Joohee
1College of Pharmacy, Duksung Women's University, 33, 144-gil, Samyang-ro, Dobong-gu, Seoul, 01369 Korea.
2Duksung Innovative Drug Center, Duksung Women's University, Seoul, Korea.
Toxicol Res. 2019 Dec 2;36(2):109-114. doi: 10.1007/s43188-019-00020-6. eCollection 2020 Apr.
Liver cancer shows noticeable differences in the incidence rate and mortality between genders. To investigate the estrogen effect on tumor progression in liver cancer, we developed a xenograft model using estrogen pellets. SK-Hep1 cells (human male liver carcinoma) were inoculated into male or female nude mice. Subsequently, estrogen pellets were subcutaneously implanted into these xenograft models. Interestingly, the marked adverse effect of estrogen pellets (0.5 mg/21 days) were observed in the male-derived xenograft model, with increased ulcerative dermatitis in male mice than in female mice. Additionally, necrosis was observed in male mice with SK-Hep1-derived tumors. However, the estrogen pellet (0.5 mg/60 days) did not exhibit these adverse effects. Tumor growth in female mice was significantly suppressed by estrogen (0.5 mg/60 days). Tumor growth was also suppressed in male mice implanted with estrogen (0.5 mg/60 days), but the suppression was not significant. We found that estrogen-induced skin damage was more severe in male mice than female mice. The tumor suppression of estrogen was effective in female mice compared to male mice bearing liver cancer. The results suggest that the sex difference affects estrogen activity and thus should be considered in the preclinical assessment.
肝癌在男女发病率和死亡率上存在显著差异。为研究雌激素对肝癌肿瘤进展的影响,我们使用雌激素药丸建立了异种移植模型。将SK-Hep1细胞(人男性肝癌细胞)接种到雄性或雌性裸鼠体内。随后,将雌激素药丸皮下植入这些异种移植模型中。有趣的是,在雄性来源的异种移植模型中观察到雌激素药丸(0.5毫克/21天)有明显的不良影响,雄性小鼠的溃疡性皮肤炎比雌性小鼠更严重。此外,在患有SK-Hep1来源肿瘤的雄性小鼠中观察到坏死。然而,雌激素药丸(0.5毫克/60天)并未表现出这些不良影响。雌激素(0.5毫克/60天)显著抑制了雌性小鼠的肿瘤生长。植入雌激素(0.5毫克/60天)的雄性小鼠的肿瘤生长也受到抑制,但抑制作用不显著。我们发现,雌激素诱导的皮肤损伤在雄性小鼠中比雌性小鼠更严重。与患有肝癌的雄性小鼠相比,雌激素对雌性小鼠的肿瘤抑制作用更有效。结果表明,性别差异会影响雌激素活性,因此在临床前评估中应予以考虑。