Inhibition effect of miR-598 on migration and invasion of non-small cell lung cancer by targeting MSI2
Objective To investigate the expression level of miR-598 in non-small cell lung cancer (NSCLC) tissues and cells lines, and determine its role on the migration and invasion of NSCLC cells. Methods The expression level of miR-598 in NSCLC tissues and cell lines was determined by real-time quantitat...
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Veröffentlicht in: | Jie fang jun yi xue za zhi 2018-09, Vol.43 (9), p.740 |
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description | Objective To investigate the expression level of miR-598 in non-small cell lung cancer (NSCLC) tissues and cells lines, and determine its role on the migration and invasion of NSCLC cells. Methods The expression level of miR-598 in NSCLC tissues and cell lines was determined by real-time quantitative PCR (qRT-PCR). The miR-598 mimics or miR-598 inhibitors were transiently transfected into A549 cells to up- or down-regulate miR-598 expression, and then the effect of miR-598 on cell migration and invasion was detected by scratch test and Transwell chamber assay. The potential binding site of miR-598 on the MSI2 was predicted by using on-line bioinformation databases, and double luciferase assay was performed to verify the targeting regulatory relationship of miR-598 to MSI2. The migration and invasive ability of A549 cells was detected after transfected with MSI2 alone or with combined MSI2 and miR-598. Results The miR-598 expression was significantly down-regulated in NSCLC tissues compared to that in parac |
doi_str_mv | 10.11855/j.issn.0577-7402.2018.09.04 |
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Methods The expression level of miR-598 in NSCLC tissues and cell lines was determined by real-time quantitative PCR (qRT-PCR). The miR-598 mimics or miR-598 inhibitors were transiently transfected into A549 cells to up- or down-regulate miR-598 expression, and then the effect of miR-598 on cell migration and invasion was detected by scratch test and Transwell chamber assay. The potential binding site of miR-598 on the MSI2 was predicted by using on-line bioinformation databases, and double luciferase assay was performed to verify the targeting regulatory relationship of miR-598 to MSI2. The migration and invasive ability of A549 cells was detected after transfected with MSI2 alone or with combined MSI2 and miR-598. Results The miR-598 expression was significantly down-regulated in NSCLC tissues compared to that in parac</description><identifier>ISSN: 0577-7402</identifier><identifier>DOI: 10.11855/j.issn.0577-7402.2018.09.04</identifier><language>chi</language><publisher>Beijing: People's Military Medical Press</publisher><subject>Binding sites ; Cell adhesion & migration ; Lung cancer</subject><ispartof>Jie fang jun yi xue za zhi, 2018-09, Vol.43 (9), p.740</ispartof><rights>2018] This work is licensed under [CC BY 3.0 Unported - https://creativecommons.org/licenses/by/3.0/ (“the License”). 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Methods The expression level of miR-598 in NSCLC tissues and cell lines was determined by real-time quantitative PCR (qRT-PCR). The miR-598 mimics or miR-598 inhibitors were transiently transfected into A549 cells to up- or down-regulate miR-598 expression, and then the effect of miR-598 on cell migration and invasion was detected by scratch test and Transwell chamber assay. The potential binding site of miR-598 on the MSI2 was predicted by using on-line bioinformation databases, and double luciferase assay was performed to verify the targeting regulatory relationship of miR-598 to MSI2. The migration and invasive ability of A549 cells was detected after transfected with MSI2 alone or with combined MSI2 and miR-598. 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Methods The expression level of miR-598 in NSCLC tissues and cell lines was determined by real-time quantitative PCR (qRT-PCR). The miR-598 mimics or miR-598 inhibitors were transiently transfected into A549 cells to up- or down-regulate miR-598 expression, and then the effect of miR-598 on cell migration and invasion was detected by scratch test and Transwell chamber assay. The potential binding site of miR-598 on the MSI2 was predicted by using on-line bioinformation databases, and double luciferase assay was performed to verify the targeting regulatory relationship of miR-598 to MSI2. The migration and invasive ability of A549 cells was detected after transfected with MSI2 alone or with combined MSI2 and miR-598. Results The miR-598 expression was significantly down-regulated in NSCLC tissues compared to that in parac</abstract><cop>Beijing</cop><pub>People's Military Medical Press</pub><doi>10.11855/j.issn.0577-7402.2018.09.04</doi></addata></record> |
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subjects | Binding sites Cell adhesion & migration Lung cancer |
title | Inhibition effect of miR-598 on migration and invasion of non-small cell lung cancer by targeting MSI2 |
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