a Department of Obstetrics and Gynecology, Shanghai First Maternity and Infant Hospital, Tongji University School of Medicine , Shanghai , China.
Cell Cycle. 2019 Aug;18(16):1925-1937. doi: 10.1080/15384101.2019.1634946. Epub 2019 Jul 10.
The high mortality of epithelial ovarian cancer (EOC) is primarily due to vast intraperitoneal dissemination. 1-calcium phosphate-uracil (1-CP-U) has previously shown the function of inhibiting migration and invasion in multiple tumor cell lines. In this study, we further assessed the possible role of 1-CP-U in suppressing the peritoneal metastasis of EOC cells. First, we demonstrated that 1-CP-U had an inhibitory effect on EOC cells in cell-matrix adhesion, migration and invasion assay . Within the model, animals were intraperitoneally inoculated with SKOV3-Luc cells and then 1-CP-U intraperitoneal (.) injection was performed every 5 d for a total of 3 wk. At the 7th d, omenta from each group were analyzed with luciferase activity and bioluminescence imaging assay, which showed a significant reduction of luciferase activity in the omenta from 1-CP-U group. In addition, the rest mice continued treatment and consistent detection of bioluminescence imaging. The data indicated that intraperitoneal metastatic nodules were less-developed in 1-CP-U group. Peritoneal metastatic tumor nodules were detected for immunofluorescent staining, which showed a reduction in FAK and p-FAK staining with 1-CP-U treatment group. Meanwhile, expressions of FAK and its downstream signaling were detected by western blot in tumor tissues and EOC cell lines, which showed significant decreases in the 1-CP-U treatment group. In conclusion, 1-CP-U had a profound inhibitory effect on adhesion, invasion and metastasis of EOC and suppressed intraperitoneal dissemination and cancer growth assay, which was associated with inhibition on the FAK pathway.
上皮性卵巢癌 (EOC) 的高死亡率主要归因于广泛的腹腔内播散。1-磷酸钙-尿嘧啶 (1-CP-U) 先前已显示出抑制多种肿瘤细胞系迁移和侵袭的功能。在本研究中,我们进一步评估了 1-CP-U 抑制 EOC 细胞腹膜转移的可能作用。首先,我们证明 1-CP-U 对细胞基质黏附、迁移和侵袭测定中的 EOC 细胞具有抑制作用。在该模型中,动物经腹腔接种 SKOV3-Luc 细胞,然后每隔 5 天进行 1-CP-U 腹腔注射,共进行 3 周。在第 7 天,用荧光素酶活性和生物发光成像分析分析各组的大网膜,结果显示 1-CP-U 组大网膜中的荧光素酶活性显著降低。此外,其余的老鼠继续接受治疗并持续进行生物发光成像检测。数据表明 1-CP-U 组腹腔转移结节发育较少。对腹膜转移性肿瘤结节进行免疫荧光染色,结果显示 1-CP-U 治疗组 FAK 和 p-FAK 染色减少。同时,通过 Western blot 检测肿瘤组织和 EOC 细胞系中的 FAK 及其下游信号表达,结果显示 1-CP-U 治疗组表达显著降低。总之,1-CP-U 对 EOC 的黏附、侵袭和转移具有深远的抑制作用,并抑制了腹膜扩散和癌症生长,这与 FAK 通路的抑制有关。