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二极管808nm GaAlAs低功率激光照射对体外抑制人肝癌细胞增殖的影响及其可能机制。

Effects of diode 808 nm GaAlAs low-power laser irradiation on inhibition of the proliferation of human hepatoma cells in vitro and their possible mechanism.

作者信息

Liu Yi-Hsiang, Cheng Chiung-Chi, Ho Chin-Chin, Pei Ren-Jeng, Lee Karen Ying, Yeh Kun-Tu, Chan You, Lai Yih-Shyong

机构信息

Center for Research and Development, Chung-tai Institute of Health Sciences and Technology, Taichung, Taiwan.

出版信息

Res Commun Mol Pathol Pharmacol. 2004;115-116:185-201.

Abstract

Low-power laser irradiation (LPLI) has come into a wide range of use in medical field. Considering basic research, LPLI can enhance DNA synthesis and increases proliferation rate of human cells. But only a few data about the effects of LPLI on human liver or hepatoma cells are available. The cytoskeleton plays important roles in cell function and therefore is implicated in the pathogenesis of many human liver diseases, including malignant tumors. In our previous study, we found the stability of cytokeratin molecules in human hepatocytes was related to the intact microtubule network that was influenced by colchicine. In this study, we are going to search the effect of LPLI on proliferation of human hepatoma cell line HepG2 and J-5 cells. In addition, the stability of cytokeratin and synemin (one of the intermediate filament-associated proteins) were analyzed under the action of LPLI to evaluate the possible mechanism of LPLI effects on proliferation of human hepatoma cells. In experiment, HepG2 and J-5 cells were cultured in 24-well plate for 24 hours. After irradiation by 130 mW diode 808 nm GaAlAs continue wave laser in different time intervals, the cell numbers were counted. Western blot and immunofluorescent staining examined the expression and distribution of PCNA, cytokeratin and synemin. The cell number counting and PCNA expression were evaluated to determine the proliferation. The organization and expression of cytokeratin and synemin were studied to identify the stability of cytoskeleton affected by LPLI. The results revealed that proliferation of HepG2 and J-5 cells was inhibited by LPLI since the cell number and PCNA expression was reduced. Maximal effect was achieved with 90 and 120 seconds of exposure time (of energy density 5.85 J/cm2 and 7.8 J/cm2, respectively) for HepG2 and J-5, respectively. The decreased ratio of cell number by this dose of irradiation was 72% and 66% in HepG2 and J-5 cells, respectively. Besides that, the architecture of intermediate filaments in these cells was disorganized by laser irradiation. The expression of intermediate filament-associated protein, synemin, was also reduced. Two significant findings are raised in this study: (1) Diode 808 nm GaAlAs continuous wave laser has an inhibitory effect on the proliferation of human hepatoma cells line HepG2 and J-5. (2) The mechanism of inhibition might be due to down-regulation of synemin expression and alteration of cytokeratin organization that was caused by laser irradiation.

摘要

低功率激光照射(LPLI)已在医学领域得到广泛应用。从基础研究来看,LPLI可增强DNA合成并提高人类细胞的增殖率。但关于LPLI对人类肝脏或肝癌细胞影响的数据却为数不多。细胞骨架在细胞功能中发挥着重要作用,因此与包括恶性肿瘤在内的许多人类肝脏疾病的发病机制有关。在我们之前的研究中,我们发现人类肝细胞中细胞角蛋白分子的稳定性与受秋水仙碱影响的完整微管网络有关。在本研究中,我们将探究LPLI对人类肝癌细胞系HepG2和J - 5细胞增殖的影响。此外,在LPLI作用下分析细胞角蛋白和丝联蛋白(中间丝相关蛋白之一)的稳定性,以评估LPLI对人类肝癌细胞增殖影响的可能机制。实验中,将HepG2和J - 5细胞接种于24孔板中培养24小时。在不同时间间隔用130 mW 808 nm二极管砷化镓铝连续波激光照射后,计数细胞数量。蛋白质免疫印迹法和免疫荧光染色检测增殖细胞核抗原(PCNA)、细胞角蛋白和丝联蛋白的表达及分布。通过评估细胞计数和PCNA表达来确定增殖情况。研究细胞角蛋白和丝联蛋白的组织及表达,以确定受LPLI影响的细胞骨架稳定性。结果显示,LPLI抑制了HepG2和J - 5细胞的增殖,因为细胞数量和PCNA表达均降低。对于HepG2和J - 5细胞,分别在照射时间为90秒和120秒(能量密度分别为5.85 J/cm²和7.8 J/cm²)时达到最大效果。此剂量照射下,HepG2和J - 5细胞的细胞数量减少比例分别为72%和66%。除此之外,激光照射使这些细胞中的中间丝结构紊乱。中间丝相关蛋白丝联蛋白的表达也降低。本研究提出了两个重要发现:(1)808 nm二极管砷化镓铝连续波激光对人类肝癌细胞系HepG2和J - 5的增殖有抑制作用。(2)抑制机制可能是由于激光照射导致丝联蛋白表达下调以及细胞角蛋白组织改变。

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