{"title":"microRNA-146a 通过 Notch1/Hes-1 信号通路对肺癌细胞的作用机制","authors":"Hui Xu, Xuan Guo, Ping Xiang, Yang Liu","doi":"","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>We explored the mechanism of action of microRNA-146a in the lung cancer cell line A549 through the Noth1/Hes-1 signal pathway.</p><p><strong>Methods: </strong>A549 cells were divided into a control NT group without transfection, NC group with transfection of miR-146a-NC, and MM group with transfection of miR-146a mimics. We employed qRT-PCR, MTT, Hoechst33258 fluorescence staining, Transwell assay, cell wound scratch assay, and Western blot for detection of the expression of miR-146a and Notch1/Hes-1, cell activity, apoptotic capacity, and invasion and migration abilities.</p><p><strong>Results: </strong>The expression of miR-146a in MM group was the highest, illustrating transfection was successful. The expression of Notch1 and Hes-1 mRNA in MM group was reduced compared to in the NC and NT groups (<i>P</i><0.05). The activity of Notch1 and Hes-1 were reduced by transfection of miR-146a as documented by the double luciferase reporter gene assay (<i>P</i><0.05). The cellular activity in the MM group was lowest after the 48 hours of culture. There was a significant difference compared with the other two groups (<i>P</i><0.05). Cell activity in the three groups after the 96 hours of culture was higher than after the 72 hours and 48 hours of culture equally (<i>P</i><0.05).</p><p><strong>Conclusion: </strong>The low expression of miR-146a could have tumor-prompting action on human NSCLC cells. Up-regulation of the expression of miR-146a restrained biological behaviors such as cell apoptosis and migration through targeted regulation involving the signal pathway of Noth1/Hes-1.</p>","PeriodicalId":8228,"journal":{"name":"Annals of clinical and laboratory science","volume":"55 1","pages":"3-9"},"PeriodicalIF":1.1000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Mechanism of Action of microRNA-146a on Lung Cancer Cells through Notch1/Hes-1 Signaling Pathway.\",\"authors\":\"Hui Xu, Xuan Guo, Ping Xiang, Yang Liu\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>We explored the mechanism of action of microRNA-146a in the lung cancer cell line A549 through the Noth1/Hes-1 signal pathway.</p><p><strong>Methods: </strong>A549 cells were divided into a control NT group without transfection, NC group with transfection of miR-146a-NC, and MM group with transfection of miR-146a mimics. We employed qRT-PCR, MTT, Hoechst33258 fluorescence staining, Transwell assay, cell wound scratch assay, and Western blot for detection of the expression of miR-146a and Notch1/Hes-1, cell activity, apoptotic capacity, and invasion and migration abilities.</p><p><strong>Results: </strong>The expression of miR-146a in MM group was the highest, illustrating transfection was successful. The expression of Notch1 and Hes-1 mRNA in MM group was reduced compared to in the NC and NT groups (<i>P</i><0.05). The activity of Notch1 and Hes-1 were reduced by transfection of miR-146a as documented by the double luciferase reporter gene assay (<i>P</i><0.05). The cellular activity in the MM group was lowest after the 48 hours of culture. There was a significant difference compared with the other two groups (<i>P</i><0.05). Cell activity in the three groups after the 96 hours of culture was higher than after the 72 hours and 48 hours of culture equally (<i>P</i><0.05).</p><p><strong>Conclusion: </strong>The low expression of miR-146a could have tumor-prompting action on human NSCLC cells. Up-regulation of the expression of miR-146a restrained biological behaviors such as cell apoptosis and migration through targeted regulation involving the signal pathway of Noth1/Hes-1.</p>\",\"PeriodicalId\":8228,\"journal\":{\"name\":\"Annals of clinical and laboratory science\",\"volume\":\"55 1\",\"pages\":\"3-9\"},\"PeriodicalIF\":1.1000,\"publicationDate\":\"2025-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Annals of clinical and laboratory science\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"MEDICAL LABORATORY TECHNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of clinical and laboratory science","FirstCategoryId":"3","ListUrlMain":"","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"MEDICAL LABORATORY TECHNOLOGY","Score":null,"Total":0}
Mechanism of Action of microRNA-146a on Lung Cancer Cells through Notch1/Hes-1 Signaling Pathway.
Objective: We explored the mechanism of action of microRNA-146a in the lung cancer cell line A549 through the Noth1/Hes-1 signal pathway.
Methods: A549 cells were divided into a control NT group without transfection, NC group with transfection of miR-146a-NC, and MM group with transfection of miR-146a mimics. We employed qRT-PCR, MTT, Hoechst33258 fluorescence staining, Transwell assay, cell wound scratch assay, and Western blot for detection of the expression of miR-146a and Notch1/Hes-1, cell activity, apoptotic capacity, and invasion and migration abilities.
Results: The expression of miR-146a in MM group was the highest, illustrating transfection was successful. The expression of Notch1 and Hes-1 mRNA in MM group was reduced compared to in the NC and NT groups (P<0.05). The activity of Notch1 and Hes-1 were reduced by transfection of miR-146a as documented by the double luciferase reporter gene assay (P<0.05). The cellular activity in the MM group was lowest after the 48 hours of culture. There was a significant difference compared with the other two groups (P<0.05). Cell activity in the three groups after the 96 hours of culture was higher than after the 72 hours and 48 hours of culture equally (P<0.05).
Conclusion: The low expression of miR-146a could have tumor-prompting action on human NSCLC cells. Up-regulation of the expression of miR-146a restrained biological behaviors such as cell apoptosis and migration through targeted regulation involving the signal pathway of Noth1/Hes-1.
期刊介绍:
The Annals of Clinical & Laboratory Science
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biotechnology, molecular biology, cytogenetics,
microbiology, immunology, hematology, transfusion
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