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罗哌卡因通过损伤线粒体和激活 caspase-3 活性促进肝癌细胞凋亡。

Ropivacaine promotes apoptosis of hepatocellular carcinoma cells through damaging mitochondria and activating caspase-3 activity.

机构信息

Hainan Provincial Key Laboratory of Carcinogenesis and Intervention, Hainan Medical College, 3 Xueyuan Road, Longhua District, Haikou, 571199, Hainan, People's Republic of China.

Department of Anaesthesiology, Second Affiliated Hospital, Hainan Medical College, Haikou, 570311, Hainan, People's Republic of China.

出版信息

Biol Res. 2019 Jul 12;52(1):36. doi: 10.1186/s40659-019-0242-7.

Abstract

BACKGROUND

Recent evidences indicated that some local anaesthetic agents played a role in inhibiting the proliferation of cancer cells; Whether ropivacaine is able to promote apoptosis of hepatocellular carcinoma (HCC) cells is still unclear. The aim of this study was to investigate the effect of ropivacaine on the apoptosis of HCC cells.

METHODS

In the present study, we treated the HCC cell lines, Bel7402 and HLE with ropivacaine. MTT, DAPI stain, trypan blue exclusion dye assay, flow cytometry, electron microscopy, computational simulation, laser confocal microscope, Western blotting, and enzyme activity analysis of caspase-3 were applied to detect the growth and apoptosis of HCC cells and to explore the role mechanism of ropivacaine.

RESULTS

Ropivacaine was able to inhibit proliferation and promote apoptosis of HCC cells in a dose- and time-dependent manner. Ropivacaine also has a trait to inhibit the migration of HCC cells; ropivacaine damaged the mitochondria of HCC cells. The results also indicated that ropivacaine was able to interact with caspase-3, promote cytoplasmic caspase-3 migration into the nucleus, stimulate cleavage of caspase-3 and PARP-1, caspase-9 proteins, inhibit the expression of Bcl-2, promote expression of Apaf-1 and mitochondria release cytochrome C, and activate the activity of caspase-3.

CONCLUSIONS

Ropivacaine has a novel role in promoting apoptosis of HCC cells; The role mechanism of ropivacaine maybe involve in damaging the function of mitochondria and activating the caspase-3 signalling pathway in HCC cells. Our findings provide novel insights into the local anaesthetic agents in the therapy of HCC patients.

摘要

背景

最近的证据表明,一些局部麻醉剂在抑制癌细胞增殖方面发挥作用;罗哌卡因是否能促进肝癌(HCC)细胞凋亡尚不清楚。本研究旨在探讨罗哌卡因对肝癌细胞凋亡的影响。

方法

在本研究中,我们用罗哌卡因处理肝癌细胞系 Bel7402 和 HLE。MTT、DAPI 染色、台盼蓝排斥染料检测、流式细胞术、电子显微镜、计算机模拟、激光共聚焦显微镜、Western blot 和 caspase-3 酶活性分析用于检测 HCC 细胞的生长和凋亡,并探讨罗哌卡因的作用机制。

结果

罗哌卡因能够以剂量和时间依赖的方式抑制 HCC 细胞的增殖并促进其凋亡。罗哌卡因还具有抑制 HCC 细胞迁移的特性;罗哌卡因损伤 HCC 细胞的线粒体。结果还表明,罗哌卡因能够与 caspase-3 相互作用,促进细胞质 caspase-3 向核内迁移,刺激 caspase-3 和 PARP-1、caspase-9 蛋白的切割,抑制 Bcl-2 的表达,促进 Apaf-1 和线粒体释放细胞色素 C 的表达,并激活 caspase-3 的活性。

结论

罗哌卡因在促进肝癌细胞凋亡方面具有新的作用;罗哌卡因的作用机制可能涉及破坏 HCC 细胞中线粒体的功能并激活 caspase-3 信号通路。我们的发现为局部麻醉剂在 HCC 患者治疗中的作用提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/340d/6625015/0e263579fc39/40659_2019_242_Fig1_HTML.jpg

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