Horita Hanane, Tsukiboshi Yosuke, Ogata Kenichi, Ogata Aya, Kurita Hisaka, Yamashita Shuji, Yamashita Hirotaka, Inagaki Naoki, Horiguchi Hyogo, Yoshioka Hiroki
Faculty of Pharmacy, Gifu University of Medical Science, 4-3-3 Nijigaoka, Kani 509-0293, Gifu, Japan.
Section of Oral and Maxillofacial Oncology, Division of Maxillofacial Diagnostic and Surgical Sciences, Faculty of Dental Science, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Fukuoka, Japan.
Plants (Basel). 2025 Apr 7;14(7):1150. doi: 10.3390/plants14071150.
Cleft palate is a common birth defect worldwide and is caused by both genetic and environmental factors. Intrauterine drug exposure is one of the environmental factors that can induce cleft palate. Mycophenolate mofetil (MPM) is an immunosuppressant drug with teratogenic effects, including cleft palate. However, the research on MPM-induced cleft palate remains limited. extract (SE), a medical plant extract, is commercially available in Asia and has been reported to show effectiveness against oral diseases. The purpose of the present study is to evaluate whether SE protects against MPM-induced immunosuppression in human embryonic palatal mesenchymal (HEPM) cells. Cell viability and G1 phase-related cell cycle markers were assessed by co-treatment with MPM and SE. Furthermore, we quantified cleft palate-associated miRNA levels and the expression of its downstream genes. MPM treatment reduced cell viability in a concentration-dependent manner. Co-treatment with SE alleviated MPM-induced inhibition of HEPM cell proliferation. Additionally, SE reduced MPM-induced upregulation and the downregulation of its downstream genes ( and ). These results suggest that SE alleviated MPM-induced cell proliferation inhibition through modulating expression.
腭裂是一种全球常见的出生缺陷,由遗传和环境因素共同导致。宫内药物暴露是可诱发腭裂的环境因素之一。霉酚酸酯(MPM)是一种具有致畸作用(包括腭裂)的免疫抑制药物。然而,关于MPM诱发腭裂的研究仍然有限。娑罗子提取物(SE)是一种药用植物提取物,在亚洲有商业销售,据报道对口腔疾病有疗效。本研究的目的是评估SE是否能保护人胚胎腭间充质(HEPM)细胞免受MPM诱导的免疫抑制。通过MPM与SE共同处理来评估细胞活力和G1期相关细胞周期标志物。此外,我们对腭裂相关的微小RNA水平及其下游基因的表达进行了定量分析。MPM处理以浓度依赖的方式降低细胞活力。SE与MPM共同处理减轻了MPM对HEPM细胞增殖的抑制作用。此外,SE降低了MPM诱导的 上调及其下游基因( 和 )的下调。这些结果表明,SE通过调节 表达减轻了MPM诱导的细胞增殖抑制。