Key Laboratory for Biorheological Science and Technology of Ministry of Education (Chongqing University), Chongqing University Cancer Hospital, Chongqing, China (mainland).
Department of Clinical Laboratory, The Traditional Chinese Medicine Hospital of Wuxi, Chongqing, China (mainland).
Med Sci Monit. 2020 Jul 31;26:e924507. doi: 10.12659/MSM.924507.
BACKGROUND Curcumin derivative C086 (cur C086) is a potential chemotherapeutic agent for patients with osteosarcoma. In this study, the effects of cur C086 combined with cisplatin on the biological processes of osteosarcoma cells were investigated. MATERIAL AND METHODS In this study, expression of BMIL1 was detected by real-time quantitative reverse transcription polymerase chain reaction and Western blotting in MG-63 cells treated with cur C086+cisplatin. Functions of cur C086+cisplatin on proliferation ability, apoptosis response, and metastatic potential of MG-63 cells were determined by MTT, flow cytometry, Hoechst 33258 staining and Transwell assays, respectively. In additionally, expression of P16, E-cadherin, epidermal growth factor (EGFR), and Notch1 was measured by Western blotting. RESULTS Expression of BMIL1 decreased significantly in MG-63 cells treated with cur C086 (20 µM)+cisplatin (1.28 nM). Treatment with cur C086+cisplatin considerably inhibited growth, migration, and invasion potential in MG-63 cells, whereas apoptosis was obviously upregulated. Moreover, cur C086+cisplatin suppressed BMIL1 expression or its potential downstream targets, P16, E-cadherin, EGFR, and Notch1. CONCLUSIONS The current results demonstrate that combined treatment with cur C086+cisplatin may be an effective form of chemotherapy for patients with osteosarcoma.
姜黄素衍生物 C086(cur C086)是骨肉瘤患者的一种潜在化疗药物。在本研究中,研究了 cur C086 联合顺铂对骨肉瘤细胞生物学过程的影响。
在本研究中,通过实时定量逆转录聚合酶链反应和 Western blot 检测 cur C086+顺铂处理的 MG-63 细胞中 BMIL1 的表达。通过 MTT、流式细胞术、Hoechst 33258 染色和 Transwell 测定分别确定 cur C086+顺铂对 MG-63 细胞增殖能力、凋亡反应和转移潜能的影响。此外,通过 Western blot 测定 P16、E-钙黏蛋白、表皮生长因子(EGF)和 Notch1 的表达。
cur C086(20µM)+顺铂(1.28nM)处理的 MG-63 细胞中 BMIL1 的表达明显降低。cur C086+顺铂处理显著抑制 MG-63 细胞的生长、迁移和侵袭能力,而凋亡明显上调。此外,cur C086+顺铂抑制了 BMIL1 表达或其潜在下游靶点 P16、E-钙黏蛋白、EGF 和 Notch1。
目前的结果表明,cur C086+顺铂联合治疗可能是骨肉瘤患者有效的化疗形式。