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Effect of docetaxel-loaded lipid microbubble in combination with ultrasound-triggered microbubble destruction on the growth of a gastric cancer cell line

机译:载有多西他赛的脂质微泡联合超声触发的微泡破坏对胃癌细胞株生长的影响

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摘要

Although gastric cancer therapy has been improved, more efficient treatment strategies still need to be developed. In the present study, a docetaxel (DOC)-loaded lipid microbubble (DLLD) was prepared and the effect of DLLD combined with ultrasound-triggered microbubble destruction (UTMD) on the growth of a gastric cancer cell line was investigated. The following four groups were included in the present study: Control, DOC, DLLD and DLLD plus UTMD. The determined entrapment efficiency of DLLD is 76±3.5%. The present study demonstrated that treatment with DLLD plus UTMD could significantly inhibit the growth of the cultured gastric cancer cell line BGC-823 via arresting the cell cycle in G2/M phase, inhibiting cell DNA synthesis, promoting cell apoptosis and disrupting mitochondrial membrane potential, as compared with treatment with DOC or DLLD alone. Furthermore, the expression of p53, p21 and Bax were identified to be significantly upregulated, while that of Bcl-2 was significantly downregulated in the DLLD plus UTMD group. Therefore, treatment with DLLD plus UTMD was more efficient in inhibiting cell proliferation and inducing cell apoptosis in the gastric cancer cell line, when compared with treatment with DOC or DLLD alone, suggesting that DLLD plus UTMD could serve as a promising strategy for the treatment of gastric cancer.
机译:尽管胃癌治疗已得到改善,但仍需要开发更有效的治疗策略。在本研究中,制备了装载多西紫杉醇(DOC)的脂质微泡(DLLD),并研究了DLLD联合超声触发的微泡破坏(UTMD)对胃癌细胞系生长的影响。本研究包括以下四组:对照,DOC,DLLD和DLLD加UTMD。所确定的DLLD的包封效率为76±3.5%。本研究表明,用DLLD加UTMD处理可以通过阻止G2 / M期的细胞周期,抑制细胞DNA合成,促进细胞凋亡并破坏线粒体膜电位来显着抑制培养的胃癌细胞BGC-823的生长,与仅使用DOC或DLLD进行治疗相比。此外,在DLLD加UTMD组中,p53,p21和Bax的表达被认为显着上调,而Bcl-2的表达被显着下调。因此,与单独使用DOC或DLLD相比,用DLLD和UTMD联合治疗在抑制胃癌细胞株中的细胞增殖和诱导细胞凋亡方面更为有效,这表明DLLD和UTMD联合治疗可以作为治疗胃癌的有前途的策略。胃癌。

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