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Experimental Study on PEG10 Antiserise Gene Therapy for Hepatocellular Carcinoma Mediated by Nanoscale Ultrasound Contrast Agent

机译:纳米级超声造影剂介导的肝细胞癌PEG10抗腐殖基因治疗的实验研究

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Objective: To explore the application of nanoscale ultrasound contrast agent mediating PEG10 antisense gene transfection in the treatment of hepatocellular carcinoma. Methods: The optimal concentration and ultrasound parameters of nanoscale ultrasound contrast agent were screened via cell viability assay. PEG10 antisense oligodeoxynucleotide (ASODN) and fluorescein-labeled specific ligand galactose terminal glycol-poly-L-lysine (G-PLL) were combined with nanoscale ultrasound contrast agent. Then PEG10 ASODN was translected into human HepG2 cells under ultrasonic irradiation. RT-PCR was used to detect the expression of PEG10. MTT assay was conducted to assess the proliferation inhibition of hepatocellular carcinoma cells. And the tumor inhibition rate in vivo was analyzed by establishing the nude mice transplantation tumor model. Results: Of all the conjugates, the optimal molar ratio of PEG10 ASODN to G-PLL was 1:2. The best parameters after screening showed that nanoscale ultrasound contrast agent of 15% microbubble concentration and ultrasound exposure at 1.5 MHz, 1.0 W/cm~2, and 10% duty cycle for 60 s had no significant influence on the viability of HepG2 cells (P > 0.05). Compared with other groups, PEG10 ASODN+G-PLL+microbubble group had the weakest PEG 10 expression, the most significant cell growth inhibition, and the highest tumor inhibition rate up to 38.5%. Conclusion: Under ultrasonic irradiation, G-PLL conjugating nanoscale microbubble ultrasound contrast agent and antisense gene can effectively enhance the inhibition of antisense gene on PEG10 expression, which has targetedly inhibitory effect on hepatoma cells. This is expected to provide an efficient means for the treatment of hepatocellular carcinoma.
机译:目的:探讨纳米级超声造影剂中介质PEG10反义基因转染治疗肝细胞癌的应用。方法:通过细胞活力测定筛选纳米级超声造影剂的最佳浓度和超声参数。将PEG10反义寡脱氧核苷酸(ASODN)和荧光素标记的特异性配体半乳糖末端二醇 - 聚-L-赖氨酸(G-PLL)与纳米级超声造影剂合并。然后在超声辐射下将PEG10 ASODN转化为人HEPG2细胞。 RT-PCR用于检测PEG10的表达。进行MTT测定以评估肝细胞癌细胞的增殖抑制。通过建立裸鼠移植肿瘤模型分析体内肿瘤抑制率。结果:在所有缀合物中,PEG10 ASODN至G-PLL的最佳摩尔比为1:2。筛选后的最佳参数表明,纳米级超声造影剂15%微泡浓度和在1.5MHz,1.0W / cm〜2的超声曝光和60℃的10%占空比对HepG2细胞的可生存率没有显着影响(P > 0.05)。与其他组相比,PEG10 ASODN + G-PLL +微胶质组具有最弱的PEG 10表达,最显着的细胞生长抑制,最高的肿瘤抑制率高达38.5%。结论:在超声波照射下,G-PLL缀合纳米级微泡超声造影剂和反义基因可以有效地增强反义基因对PEG10表达的抑制,这对肝癌细胞具有靶向抑制作用。这预计将提供治疗肝细胞癌的有效手段。

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