首页> 外文期刊>Journal of Cancer >Amide-type local anesthetics may suppress tumor cell proliferation and sensitize Human Hepatocellular Carcinoma Cells to Cisplatin via upregulation of RASSF1A expression and demethylation
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Amide-type local anesthetics may suppress tumor cell proliferation and sensitize Human Hepatocellular Carcinoma Cells to Cisplatin via upregulation of RASSF1A expression and demethylation

机译:酰胺型局部麻醉剂可通过摇滚表达和去甲基化的上调来抑制肿瘤细胞增殖并使人肝细胞癌细胞敏化为顺铂

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Background: It has been reported that local anesthetics are toxic to various types of cells. Furthermore, several local anesthetics have been confirmed to exert demethylation effects and regulate the proliferation of human cancer cells. Our previous findings suggest that lidocaine may exert potential antitumor activity and enhance the sensitivity of cisplatin to hepatocellular carcinoma in vitro and in vivo. A recent study proved that lidocaine sensitizes breast cancer cells to cisplatin via upregulation of RASSF1A, a promotor of tumor suppressive gene (TSG) demethylation. We sought to determine whether amide-type local anesthetics (lidocaine, ropivacaine and bupivacaine) exert growth-inhibitory effects on human hepatoma cells and to determine whether amide-type local anesthetics sensitize human hepatoma cells to cisplatin-mediated cytotoxicity via upregulation of RASSF1A expression. Methods: Human hepatoma cell lines HepG2 and BEL-7402 were incubated with lidocaine, ropivacaine and bupivacaine. The viability of local anesthetic-treated cells with or without cisplatin was investigated. Further, we evaluated RASSF1A expression after treatment of HepG2 and BEL-7402 cells with three local anesthetics and determined the influence of RASSF1A expression on the toxicity of cisplatin to these cells. Results: The viability of HepG2 and BEL-7402 cells was significantly decreased by treatment with amide-type local anesthetics (lidocaine, ropivacaine and bupivacaine). In these cells, the combination treatment with cisplatin and local anesthetics exhibited a stronger reduction in viability. Lidocaine, ropivacaine and bupivacaine promoted a significant increase in RASSF1A expression and a decrease in RASSF1A methylation. The combined treatment with both local anesthetics and cisplatin resulted in a significantly lower level of HepG2 and BEL-7402 cell viability than that with singular local anesthetics or cisplatin treatment. Moreover, local anesthetics enhanced the cytotoxicity of cisplatin against HepG2 and BEL-7402 cells, accompanied by an increase in RASSF1A expression. Conclusions: These data indicated that amide-type local anesthetics (lidocaine, ropivacaine and bupivacaine) have growth-inhibitory and demethylation effects in human hepatoma cells. We also found that these amide local anesthetics may enhance the cytotoxicity of cisplatin in human hepatocellular carcinoma cells possibly via upregulation of RASSF1A expression and demethylation.? The author(s).
机译:背景:据报道,局部麻醉剂对各种类型的细胞有毒。此外,已经证实了几种局部麻醉剂施加去甲基化作用并调节人癌细胞的增殖。我们以前的研究结果表明,利多卡因可能发挥潜在的抗肿瘤活性,并增强顺铂在体外和体内肝细胞癌对肝细胞癌的敏感性。最近的一项研究证明,利多卡因通过rassf1a的上调,肿瘤抑制基因(TSG)去甲基化的促进剂来使乳腺癌细胞敏感到顺铂。我们试图确定酰胺型局部麻醉剂(利多卡因,罗比卡因和Bupivacaine)对人肝癌细胞产生生长抑制作用,并确定酰胺型局部麻醉剂是否通过RASSF1a表达的上调致敏于人肝癌细胞毒性的顺铂介导的细胞毒性。方法:人肝癌细胞系HepG2和Bel-7402与Lidocaine,Ropivacaine和Bupivacaine一起温育。研究了局部麻醉处理的细胞的可行性或没有顺铂的可行性。此外,我们在用三种局部麻醉剂治疗HepG2和Bel-7402细胞后评估RASSF1A表达,并确定RASSF1a表达对这些细胞的顺铂毒性的影响。结果:通过酰胺型局部麻醉剂(Lidocaine,Ropivacaine和Bupivacaine)治疗,HepG2和Bel-7402细胞的可行性显着降低。在这些细胞中,用顺铂和局部麻醉剂的组合治疗表现出更强的活力减少。利多卡因,罗哌卡因和布比卡因促进了rassf1a表达的显着增加和rassf1a甲基化的减少。与局部麻醉剂和顺铂的合并治疗导致HEPG2和BEPG2和BEP-7402细胞活力显着较低,与单数局部麻醉剂或顺铂治疗。此外,局部麻醉剂增强了顺铂对抗HepG2和Bel-7402细胞的细胞毒性,伴随着Rassf1a表达的增加。结论:这些数据表明,酰胺型局部麻醉剂(利多卡因,罗比卡因和Bupivacaine)具有人肝癌细胞的生长抑制和去甲基化作用。我们还发现,这些酰胺局部麻醉剂可能通过rassf1a表达和去甲基化的上调提高人肝细胞癌细胞中顺铂的细胞毒性。作者。

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