Study of the Effect of Linoleic Acid on the Expression Level of MicroRNA-106b and MicroRNA-20a and their Related Target MHC Class I Chain-related Protein A in Docetaxel-treated Gastric Cancer Cells

IF 0.4 Q4 ONCOLOGY
N. Shekari, Tohid Kazemi, Maedeh Moradi, E. Eghbali, B. Sepehri, V. K. Shahgoli, M. Shirmohamadi
{"title":"Study of the Effect of Linoleic Acid on the Expression Level of MicroRNA-106b and MicroRNA-20a and their Related Target MHC Class I Chain-related Protein A in Docetaxel-treated Gastric Cancer Cells","authors":"N. Shekari, Tohid Kazemi, Maedeh Moradi, E. Eghbali, B. Sepehri, V. K. Shahgoli, M. Shirmohamadi","doi":"10.30476/MEJC.2021.87303.1406","DOIUrl":null,"url":null,"abstract":"Background: MicroRNAs are involved in response to therapeutic agents and have the ability to regulate the expression level of the targets associated with cancer growth and progression. As a dangerous signal in tumor cells, increased expression level of MHC class I chain-related protein A (MICA) could activate the immune system and induce responses to tumor cells. We conducted the present research to study the effect of linoleic acid (LA) and docetaxel alone or in combination with miR-106b, miR-20a, and MICA expression level in metastatic gastric cancer (GC) cell line, MKN-45. Method: The study was an in vitro study using the gastric cancer cell line MKN-45, which was cultured and treated with docetaxel and LA. Subsequently, the expression level of miR-106b, miR-20a, and MICA were assessed with quantitative real-time PCR. Results: MiR-106b decreased in LA and LA/docetaxel (p p =0.002), and increased in docetaxel alone (p =0.01). Meanwhile, miR-20a significantly decreased in docetaxel and LA/docetaxel (p <0.0001), increased in LA treatment (p =0.02). Regarding MICA, it significantly decreased in all the treated cells (p <0.0001, p <0.0001, and p =0.0002 for docetaxel, LA and docetaxel/LA, respectively) but with different reduction intensities. Conclusion: Using LA or docetaxel alone had a different effect on miR-106b, miR-20a, and MICA expression level, yet in a simultaneous treatment, their positive effects were intensified. LA enhanced the effect of docetaxel concerning the expression level of miR-106b, miR-20a, and MICA and vice versa, which suggested that LA could be employed as an effective complementary agent in GC along with docetaxel.","PeriodicalId":44005,"journal":{"name":"Middle East Journal of Cancer","volume":" ","pages":""},"PeriodicalIF":0.4000,"publicationDate":"2021-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Middle East Journal of Cancer","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.30476/MEJC.2021.87303.1406","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: MicroRNAs are involved in response to therapeutic agents and have the ability to regulate the expression level of the targets associated with cancer growth and progression. As a dangerous signal in tumor cells, increased expression level of MHC class I chain-related protein A (MICA) could activate the immune system and induce responses to tumor cells. We conducted the present research to study the effect of linoleic acid (LA) and docetaxel alone or in combination with miR-106b, miR-20a, and MICA expression level in metastatic gastric cancer (GC) cell line, MKN-45. Method: The study was an in vitro study using the gastric cancer cell line MKN-45, which was cultured and treated with docetaxel and LA. Subsequently, the expression level of miR-106b, miR-20a, and MICA were assessed with quantitative real-time PCR. Results: MiR-106b decreased in LA and LA/docetaxel (p p =0.002), and increased in docetaxel alone (p =0.01). Meanwhile, miR-20a significantly decreased in docetaxel and LA/docetaxel (p <0.0001), increased in LA treatment (p =0.02). Regarding MICA, it significantly decreased in all the treated cells (p <0.0001, p <0.0001, and p =0.0002 for docetaxel, LA and docetaxel/LA, respectively) but with different reduction intensities. Conclusion: Using LA or docetaxel alone had a different effect on miR-106b, miR-20a, and MICA expression level, yet in a simultaneous treatment, their positive effects were intensified. LA enhanced the effect of docetaxel concerning the expression level of miR-106b, miR-20a, and MICA and vice versa, which suggested that LA could be employed as an effective complementary agent in GC along with docetaxel.
亚油酸对多西他赛处理胃癌细胞中MicroRNA-106b、MicroRNA-20a及其相关靶MHC I类链相关蛋白A表达水平的影响研究
背景:MicroRNAs参与对治疗药物的反应,并具有调节与癌症生长和进展相关的靶标表达水平的能力。MHC I类链相关蛋白a (MICA)作为肿瘤细胞中的危险信号,其表达水平升高可激活免疫系统,诱导对肿瘤细胞的应答。我们进行了本研究,研究亚油酸(LA)和多西他赛单独或联合miR-106b、miR-20a和MICA表达水平对转移性胃癌(GC)细胞系MKN-45的影响。方法:采用体外培养的胃癌细胞株MKN-45,经多西紫杉醇和LA处理。随后,采用实时荧光定量PCR检测miR-106b、miR-20a和MICA的表达水平。结果:MiR-106b在LA和LA/多西紫杉醇组中降低(p p =0.002),而在多西紫杉醇组中升高(p =0.01)。同时,miR-20a在多西他赛和LA/多西他赛组中显著降低(p <0.0001),在LA组中升高(p =0.02)。MICA在所有处理细胞中均显著降低(多西他赛、LA和多西他赛/LA分别为p <0.0001、p <0.0001和p =0.0002),但降低程度不同。结论:LA与多西紫杉醇单用对miR-106b、miR-20a、MICA表达水平的影响不同,但同时使用时,其阳性作用增强。LA增强了多西他赛对miR-106b、miR-20a和MICA表达水平的影响,反之亦然,这表明LA可以与多西他赛一起作为GC的有效补充剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
0.80
自引率
0.00%
发文量
0
审稿时长
12 weeks
期刊介绍: Middle East Journal of Cancer (MEJC) is an international peer-reviewed journal which aims to publish high-quality basic science and clinical research in the field of cancer. This journal will also reflect the current status of research as well as diagnostic and treatment practices in the field of cancer in the Middle East, where cancer is becoming a growing health problem. Lastly, MEJC would like to become a model for regional journals with an international outlook. Accordingly, manuscripts from authors anywhere in the world will be considered for publication. MEJC will be published on a quarterly basis.
×
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