酮咯酸通过胰岛素样生长因子2信号通路抑制卵巢癌的生长和转移

目的 探讨酮咯酸对卵巢癌生长、转移影响及机制。方法 实验于2019年8月至2020年3月进行。细胞计数试剂盒（CCK-8）法检测不同剂量（0.10 g/L、0.50 g/L、1.00 g/L、1.50 g/L）酮咯酸对人卵巢癌细胞SKOV3的抑制率，筛选酮咯酸的最佳作用浓度。SKOV3细胞分为NC组、酮咯酸组、DMSO组、Linsitinib组、酮咯酸+pcDNA 3.1组和酮咯酸+pcDNA 3.1-IGF2组，TraNCwell法检测各组细胞迁移和侵袭，蛋白质印迹法（Western blotting）法检测各组细胞中胰岛素样生长因子2(IGF2)、胰岛素样生长因子1受体（IGF1R）的蛋白表达。裸鼠分为NC组和酮咯酸组，每组10只，观察酮咯酸对肿瘤生长及肿瘤组织中IGF2、IGF1R的蛋白表达的影响。结果 与NC组相比，不同剂量（0.10、0.50、1.00、1.50 g/L）酮咯酸组细胞抑制率升高（6.99±0.06）%、（23.31±2.11）%、（51.39±6.91）%、（76.14±4.36）%比（0.02±0.00）%,P <0.05]，选择1.0 g/L酮咯酸...

Ketorolac inhibits ovarian cancer growth and metastasis via IGF2 signaling pathway

Objective To investigate the effect of ketorolac on the growth and metastasis of ovarian cancer and its mechanism.Meth? ods Experiments were conducted from August 2019 to March 2020. Cell counting kit (CCK-8) method was used to detect the inhibition rates of ketorolac (0.10 g/L, 0.50 g/L, 1.00 g/L, 1.50 g/L) on human ovarian cancer cell line SKOV3. The optimal concentration ofketorolac was sorted out. Patients were assigned into NC group, ketorolac group, DMSO group, Linsitinib group, ketorolac + pcDNA 3.1group and ketorolac + pcDNA3.1-IGF2 group. Cell migration and invasion were detected by TraNCwell, the protein expressions of insulin-like growth factor 2 (IGF2) and insulin-like growth factor 1 receptor (IGF1R) were detected by western blotting. Nude mice were assigned into NC group and ketorolac group, with 10 in each group. Observation was made of the effect of ketorolac on tumor growth andprotein expressions of IGF2 and IGF1R in tumor tissue.Results Compared with the NC group, the cell inhibition rates of ketorolacgroups at different doses (0.10 g/L, 0.50 g/L, 1.00 g/L, 1.50 g/L) increased (6.99±0.06) %, (23.31±2.11) %, (51.39±6.91) %, (76.14±4.36) % vs. (0.02±0.00) %, P<0.05], and 1.00 g/L of ketorolac was selected as the best concentration. Compared with the NC group, thenumber of cell migration (54±5) vs. (103±9)], the number of invasion (41±4) vs. (76±6)] and the protein expressions of IGF2 (0.31± 0.03) vs. (1.01±0.06)] and IGF1R (0.26±0.02) vs. (0.99±0.08)] in the ketorolac groups were significantly reduced (all P<0.05). Compared with the NC group or the DMSO group, the number of cell migration (63±6) vs. (98±9), (99±7)], the number of invasion (51±5) vs. (73±5), (75±6)] and the protein expressions of IGF2 (0.28±0.02) vs. (0.98±0.05), (1.00±0.07)] and IGF1R (0.29±0.02) vs. (0.99± 0.06), (1.02±0.08)] in the Linsitinib group were significantly reduced (all P<0.05). Compared with the ketorolac group or the ketorolac+pcDNA 3.1 group, the number of cell migration (87±7) vs. (52±5), (53±5)], the number of cell invasion (75±6) vs. (44±4), (42±4)] and the protein expressions of IGF2 (1.28±0.13) vs. (0.31±0.03), (0.33±0.04)] and IGF1R (1.19±0.12) vs. (0.26±0.02), (0.27±0.03)] in the ketorolac+pcDNA 3.1-IGF2 group were significantly increased (all P<0.05). Compared with the NC group, the weight (0.53±0.05) g vs. (1.01±0.07) g] and volume (0.55±0.05) cm3 vs. (1.00±0.04) cm3] of the nude mouse tumors in the ketorolac group were significantly reduced (both P<0.05), and the protein expressions of IGF2 (0.46±0.04) vs. (0.99±0.08)] and IGF1R (0.52±0.05) vs. (0.97±0.09)] in tumor tissue were significantly reduced (both P<0.05).Conclusion Ketorolac can inhibit the migration and invasion of ovarian cancercells in vitro and tumor growth in vivo, and its mechanism may be related to the inhibition of IGF2 signaling pathway.