建立顺铂耐药胃癌细胞株MGC-803/顺铂,并揭示其作用机制

Jin-lu Liu, K. Zhao, Y. Qiu, Zhen Wang, Yuan-tian Mao, Bo-pei Li, Yeyang Chen
{"title":"建立顺铂耐药胃癌细胞株MGC-803/顺铂,并揭示其作用机制","authors":"Jin-lu Liu, K. Zhao, Y. Qiu, Zhen Wang, Yuan-tian Mao, Bo-pei Li, Yeyang Chen","doi":"10.3760/CMA.J.ISSN.1001-9030.2019.12.022","DOIUrl":null,"url":null,"abstract":"Objective \nTo establish a cisplatin-resistant gastric cancer cell line MGC-803/cisplatin (DDP) and to explore its drug resistance mechanism. \n \n \nMethods \nThe cisplatin was used to induce the drug resistance of MGC-803 cells. The half maximal inhibitory concentration (IC50) of the drug-resistant strains was detected by the cell counting kit-8 (CCK-8) method. The expression of chloride intracellular channel 1 (CLIC1) was detected by Western blotting analyses. The wild-type CLIC1 plasmid and the short hairpin RNA (shRNA) plasmid targeting CLIC1 were constructed. After Lipo3000 was transfected into gastric cancer cells, the IC50 of gastric cancer cells to cisplatin was detected, and then the intracellular Cl-concentration was detected by MQAE fluorescent probe. \n \n \nResults \nThe cisplatin-resistant cell line MGC-803/DDP was successfully induced with an IC50 of (7.02±0.13) mg/L, while the IC50 of MGC803 was (1.29±0.09) mg/L, (t=36.090, P<0.05). The CLIC1 protein of MGC803/DDP was up-regulated by (2.27±0.15) times relative to MGC803 (t=7.841, P<0.05). After silencing the CLIC1 gene of MGC803/DDP, the IC50 of the CON, CN, and KD groups were (6.96±0.09), (6.93±0.15) and (3.02±0.20) mg/L, respectively, which was significantly decreased in the KD group (F=0.209, P<0.05). After overexpression of the CLIC1 gene in MGC803 cells, the IC50 of the CON, CN, and OE groups were (1.35±0.07), (1.25±0.07) and (4.77±0.12) mg/L, respectively, and the OE group was significantly elevated (F=0.508, P<0.05). The concentration of chloride ion was detected by MQAE. The relative fluorescence intensity of MGC-803, MGC-803/OE, MGC-803/DDP and MGC-803/DDP-KD were (1.02±0.03), (0.61±0.02), (0.67±0.01) and (1.39±0.02), respectively. The concentration of Cl- in MGC-803/OE cells was higher than that in MGC-803 (t=10.800, P<0.05), while the concentration of Cl- in MGC-803/DDP was higher than that in MGC-803 and MGC-803/DDP-KD, and the concentration of Cl- in KD group was the lowest (F=229, P<0.05). \n \n \nConclusion \nThe CLIC1 gene can induce the resistance of gastric cancer cell line MGC-803 to cisplatin in vitro. The mechanism may be related to the up-regulation of CLIC1 expression, which leads to an increase of intracellular chloride ion concentration. \n \n \nKey words: \nGastric cancer; Chloride intracellular channel 1; Cisplatin; Drug resistance","PeriodicalId":10065,"journal":{"name":"中华实验外科杂志","volume":"36 1","pages":"2200-2202"},"PeriodicalIF":0.0000,"publicationDate":"2019-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Establish cisplatin-resistant gastric cancer cell line MGC-803/cisplatin and reveal its mechanism\",\"authors\":\"Jin-lu Liu, K. Zhao, Y. Qiu, Zhen Wang, Yuan-tian Mao, Bo-pei Li, Yeyang Chen\",\"doi\":\"10.3760/CMA.J.ISSN.1001-9030.2019.12.022\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Objective \\nTo establish a cisplatin-resistant gastric cancer cell line MGC-803/cisplatin (DDP) and to explore its drug resistance mechanism. \\n \\n \\nMethods \\nThe cisplatin was used to induce the drug resistance of MGC-803 cells. The half maximal inhibitory concentration (IC50) of the drug-resistant strains was detected by the cell counting kit-8 (CCK-8) method. The expression of chloride intracellular channel 1 (CLIC1) was detected by Western blotting analyses. The wild-type CLIC1 plasmid and the short hairpin RNA (shRNA) plasmid targeting CLIC1 were constructed. After Lipo3000 was transfected into gastric cancer cells, the IC50 of gastric cancer cells to cisplatin was detected, and then the intracellular Cl-concentration was detected by MQAE fluorescent probe. \\n \\n \\nResults \\nThe cisplatin-resistant cell line MGC-803/DDP was successfully induced with an IC50 of (7.02±0.13) mg/L, while the IC50 of MGC803 was (1.29±0.09) mg/L, (t=36.090, P<0.05). The CLIC1 protein of MGC803/DDP was up-regulated by (2.27±0.15) times relative to MGC803 (t=7.841, P<0.05). After silencing the CLIC1 gene of MGC803/DDP, the IC50 of the CON, CN, and KD groups were (6.96±0.09), (6.93±0.15) and (3.02±0.20) mg/L, respectively, which was significantly decreased in the KD group (F=0.209, P<0.05). After overexpression of the CLIC1 gene in MGC803 cells, the IC50 of the CON, CN, and OE groups were (1.35±0.07), (1.25±0.07) and (4.77±0.12) mg/L, respectively, and the OE group was significantly elevated (F=0.508, P<0.05). The concentration of chloride ion was detected by MQAE. The relative fluorescence intensity of MGC-803, MGC-803/OE, MGC-803/DDP and MGC-803/DDP-KD were (1.02±0.03), (0.61±0.02), (0.67±0.01) and (1.39±0.02), respectively. The concentration of Cl- in MGC-803/OE cells was higher than that in MGC-803 (t=10.800, P<0.05), while the concentration of Cl- in MGC-803/DDP was higher than that in MGC-803 and MGC-803/DDP-KD, and the concentration of Cl- in KD group was the lowest (F=229, P<0.05). \\n \\n \\nConclusion \\nThe CLIC1 gene can induce the resistance of gastric cancer cell line MGC-803 to cisplatin in vitro. The mechanism may be related to the up-regulation of CLIC1 expression, which leads to an increase of intracellular chloride ion concentration. \\n \\n \\nKey words: \\nGastric cancer; Chloride intracellular channel 1; Cisplatin; Drug resistance\",\"PeriodicalId\":10065,\"journal\":{\"name\":\"中华实验外科杂志\",\"volume\":\"36 1\",\"pages\":\"2200-2202\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-12-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"中华实验外科杂志\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.3760/CMA.J.ISSN.1001-9030.2019.12.022\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"中华实验外科杂志","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3760/CMA.J.ISSN.1001-9030.2019.12.022","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

目的建立顺铂耐药胃癌细胞株MGC-803/顺铂(DDP),并探讨其耐药机制。方法采用顺铂诱导MGC-803细胞耐药。采用细胞计数试剂盒-8 (CCK-8)法检测耐药菌株的半数最大抑制浓度(IC50)。Western blotting检测细胞内氯离子通道1 (CLIC1)的表达。构建了野生型CLIC1质粒和靶向CLIC1的短发夹RNA (shRNA)质粒。Lipo3000转染胃癌细胞后,检测胃癌细胞对顺铂的IC50,然后用MQAE荧光探针检测细胞内cl浓度。结果成功诱导顺铂耐药细胞株MGC-803/DDP, IC50为(7.02±0.13)mg/L,而MGC803的IC50为(1.29±0.09)mg/L, (t=36.090, P<0.05)。MGC803/DDP的CLIC1蛋白表达量较MGC803上调(2.27±0.15)倍(t=7.841, P<0.05)。沉默MGC803/DDP CLIC1基因后,CON组、CN组和KD组的IC50分别为(6.96±0.09)、(6.93±0.15)和(3.02±0.20)mg/L, KD组的IC50显著降低(F=0.209, P<0.05)。CLIC1基因在MGC803细胞中过表达后,CON、CN、OE组的IC50分别为(1.35±0.07)、(1.25±0.07)、(4.77±0.12)mg/L, OE组显著升高(F=0.508, P<0.05)。采用MQAE法检测氯离子浓度。MGC-803、MGC-803/OE、MGC-803/DDP和MGC-803/DDP- kd的相对荧光强度分别为(1.02±0.03)、(0.61±0.02)、(0.67±0.01)和(1.39±0.02)。MGC-803/OE细胞Cl-浓度高于MGC-803组(t=10.800, P<0.05), MGC-803/DDP细胞Cl-浓度高于MGC-803和MGC-803/DDP-KD组,且KD组Cl-浓度最低(F=229, P<0.05)。结论CLIC1基因可诱导胃癌细胞株MGC-803体外对顺铂耐药。其机制可能与CLIC1表达上调导致细胞内氯离子浓度升高有关。关键词:胃癌;细胞内氯离子通道1;顺铂;耐药性
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Establish cisplatin-resistant gastric cancer cell line MGC-803/cisplatin and reveal its mechanism
Objective To establish a cisplatin-resistant gastric cancer cell line MGC-803/cisplatin (DDP) and to explore its drug resistance mechanism. Methods The cisplatin was used to induce the drug resistance of MGC-803 cells. The half maximal inhibitory concentration (IC50) of the drug-resistant strains was detected by the cell counting kit-8 (CCK-8) method. The expression of chloride intracellular channel 1 (CLIC1) was detected by Western blotting analyses. The wild-type CLIC1 plasmid and the short hairpin RNA (shRNA) plasmid targeting CLIC1 were constructed. After Lipo3000 was transfected into gastric cancer cells, the IC50 of gastric cancer cells to cisplatin was detected, and then the intracellular Cl-concentration was detected by MQAE fluorescent probe. Results The cisplatin-resistant cell line MGC-803/DDP was successfully induced with an IC50 of (7.02±0.13) mg/L, while the IC50 of MGC803 was (1.29±0.09) mg/L, (t=36.090, P<0.05). The CLIC1 protein of MGC803/DDP was up-regulated by (2.27±0.15) times relative to MGC803 (t=7.841, P<0.05). After silencing the CLIC1 gene of MGC803/DDP, the IC50 of the CON, CN, and KD groups were (6.96±0.09), (6.93±0.15) and (3.02±0.20) mg/L, respectively, which was significantly decreased in the KD group (F=0.209, P<0.05). After overexpression of the CLIC1 gene in MGC803 cells, the IC50 of the CON, CN, and OE groups were (1.35±0.07), (1.25±0.07) and (4.77±0.12) mg/L, respectively, and the OE group was significantly elevated (F=0.508, P<0.05). The concentration of chloride ion was detected by MQAE. The relative fluorescence intensity of MGC-803, MGC-803/OE, MGC-803/DDP and MGC-803/DDP-KD were (1.02±0.03), (0.61±0.02), (0.67±0.01) and (1.39±0.02), respectively. The concentration of Cl- in MGC-803/OE cells was higher than that in MGC-803 (t=10.800, P<0.05), while the concentration of Cl- in MGC-803/DDP was higher than that in MGC-803 and MGC-803/DDP-KD, and the concentration of Cl- in KD group was the lowest (F=229, P<0.05). Conclusion The CLIC1 gene can induce the resistance of gastric cancer cell line MGC-803 to cisplatin in vitro. The mechanism may be related to the up-regulation of CLIC1 expression, which leads to an increase of intracellular chloride ion concentration. Key words: Gastric cancer; Chloride intracellular channel 1; Cisplatin; Drug resistance
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
18226
期刊介绍:
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信