Marasovic Maja, Ivankovic Sinisa, Stojkovic Ranko, Djermic Damir, Galic Borivoj, Milos Mladen
a Faculty of Chemistry and Technology , University of Split , Split , Croatia.
b Division of Molecular Medicine , Rudjer Boskovic Institute , Zagreb , Croatia.
J Enzyme Inhib Med Chem. 2017 Dec;32(1):1299-1304. doi: 10.1080/14756366.2017.1384823.
The cytotoxic activity of phenylboroxine acid was evaluated in vitro on mouse mammary adenocarcinoma 4T1, mouse squamous cell carcinoma SCCVII, hamster lung fibroblast V79 and mouse dermal fibroblasts L929 cell lines. The cytotoxic effects were dose dependent for all tested tumour and non-tumour cell lines. Under in vivo conditions, three application routes of phenylboronic acid were studied: intra-peritoneal (i.p.), intra-tumour (i.t.) and per-oral. After tumour transplantation in syngeneic mice, phenylboronic acid was shown to slow the growth of both tumour cell lines (4T1 and SCCVII) compared with the control. The inhibitory effects were pronounced during the application of phenylboronic acid. For both tested tumour cell lines, the most prominent antitumour effect was obtained by intraperitoneal administration, followed significantly by oral administration.
在体外对小鼠乳腺腺癌4T1、小鼠鳞状细胞癌SCCVII、仓鼠肺成纤维细胞V79和小鼠皮肤成纤维细胞L929细胞系评估了苯硼酸的细胞毒性活性。对于所有测试的肿瘤和非肿瘤细胞系,细胞毒性作用均呈剂量依赖性。在体内条件下,研究了苯硼酸的三种给药途径:腹腔内(i.p.)、肿瘤内(i.t.)和口服。在同基因小鼠中进行肿瘤移植后,与对照组相比,苯硼酸显示出可减缓两种肿瘤细胞系(4T1和SCCVII)的生长。在应用苯硼酸期间,抑制作用明显。对于两种测试的肿瘤细胞系,腹腔内给药获得了最显著的抗肿瘤效果,其次是口服给药,其效果明显次之。