MiR-889 promotes cell growth in human non-small cell lung cancer by regulating KLF9

Currently, non-small cell lung cancer (NSCLC) is still the most common malignancy worldwide. Although miR-889 has been reported to play an important role in various malignancies, the physiological function of miR-889 in NSCLC remains unknown. This paper places emphasis on the influence of miR-889 on...

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Veröffentlicht in:Gene 2019-05, Vol.699, p.94-101
Hauptverfasser: Han, Xu, Tang, Yihu, Dai, Yawei, Hu, Shuai, Zhou, Jingxin, Liu, Xiang, Zhu, Jinfu, Wu, Yanhu
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container_title Gene
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creator Han, Xu
Tang, Yihu
Dai, Yawei
Hu, Shuai
Zhou, Jingxin
Liu, Xiang
Zhu, Jinfu
Wu, Yanhu
description Currently, non-small cell lung cancer (NSCLC) is still the most common malignancy worldwide. Although miR-889 has been reported to play an important role in various malignancies, the physiological function of miR-889 in NSCLC remains unknown. This paper places emphasis on the influence of miR-889 on the development and progression of non-small cell lung cancer. To detect the expression level of miR-889 in NSCLC tissues and cell lines, quantitative real-time polymerase chain reaction (qRT-PCR) assay and In Situ Hybridization (ISH) were adopted in this study. Cell proliferation and colony forming ability were examined by Cell Counting Kit-8 (CCK-8) and colony formation assays. Furthermore, transwell experiments were conducted to determine the influence of miR-889 on migration. KLF9 expression was evaluated by qRT-PCR and Western blotting. First, miR-889 expression was increased in the cancer tissues of non-small cell lung cancer patients (n = 40) compared with adjacent tissues. Subsequently, knockdown of miR-889 significantly inhibited cell proliferation and migration, while overexpression of miR-889 had the opposite effect. KLF9 may be a potential target of miR-889. In addition, upregulation of miR-889 promotes tumorigenesis in vitro, and KLF9 protein levels are also reduced. The current study suggests that miR-889 may play a potential therapeutic role for NSCLC by targeting KLF9 to control NSCLC proliferation and migration. •miR-889 play an important role in NSCLC.•miR-889 promotes NSCLC cell proliferation and migration by regulating KLF9.•miR-889 may become a new targeted therapy for lung cancer.
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Although miR-889 has been reported to play an important role in various malignancies, the physiological function of miR-889 in NSCLC remains unknown. This paper places emphasis on the influence of miR-889 on the development and progression of non-small cell lung cancer. To detect the expression level of miR-889 in NSCLC tissues and cell lines, quantitative real-time polymerase chain reaction (qRT-PCR) assay and In Situ Hybridization (ISH) were adopted in this study. Cell proliferation and colony forming ability were examined by Cell Counting Kit-8 (CCK-8) and colony formation assays. Furthermore, transwell experiments were conducted to determine the influence of miR-889 on migration. KLF9 expression was evaluated by qRT-PCR and Western blotting. First, miR-889 expression was increased in the cancer tissues of non-small cell lung cancer patients (n = 40) compared with adjacent tissues. Subsequently, knockdown of miR-889 significantly inhibited cell proliferation and migration, while overexpression of miR-889 had the opposite effect. KLF9 may be a potential target of miR-889. In addition, upregulation of miR-889 promotes tumorigenesis in vitro, and KLF9 protein levels are also reduced. The current study suggests that miR-889 may play a potential therapeutic role for NSCLC by targeting KLF9 to control NSCLC proliferation and migration. •miR-889 play an important role in NSCLC.•miR-889 promotes NSCLC cell proliferation and migration by regulating KLF9.•miR-889 may become a new targeted therapy for lung cancer.</description><identifier>ISSN: 0378-1119</identifier><identifier>EISSN: 1879-0038</identifier><identifier>DOI: 10.1016/j.gene.2019.02.077</identifier><identifier>PMID: 30849540</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>A549 Cells ; Carcinoma, Non-Small-Cell Lung - genetics ; Cell Line, Tumor ; Cell Movement - genetics ; Cell Proliferation - genetics ; Gene Expression Regulation, Neoplastic - genetics ; Humans ; KLF9 ; Kruppel-Like Transcription Factors - genetics ; Lung Neoplasms - genetics ; MicroRNAs - genetics ; Migration ; miR-889 ; NSCLC ; Proliferation ; Up-Regulation - genetics</subject><ispartof>Gene, 2019-05, Vol.699, p.94-101</ispartof><rights>2019</rights><rights>Copyright © 2019. 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Subsequently, knockdown of miR-889 significantly inhibited cell proliferation and migration, while overexpression of miR-889 had the opposite effect. KLF9 may be a potential target of miR-889. In addition, upregulation of miR-889 promotes tumorigenesis in vitro, and KLF9 protein levels are also reduced. The current study suggests that miR-889 may play a potential therapeutic role for NSCLC by targeting KLF9 to control NSCLC proliferation and migration. •miR-889 play an important role in NSCLC.•miR-889 promotes NSCLC cell proliferation and migration by regulating KLF9.•miR-889 may become a new targeted therapy for lung cancer.</description><subject>A549 Cells</subject><subject>Carcinoma, Non-Small-Cell Lung - genetics</subject><subject>Cell Line, Tumor</subject><subject>Cell Movement - genetics</subject><subject>Cell Proliferation - genetics</subject><subject>Gene Expression Regulation, Neoplastic - genetics</subject><subject>Humans</subject><subject>KLF9</subject><subject>Kruppel-Like Transcription Factors - genetics</subject><subject>Lung Neoplasms - genetics</subject><subject>MicroRNAs - genetics</subject><subject>Migration</subject><subject>miR-889</subject><subject>NSCLC</subject><subject>Proliferation</subject><subject>Up-Regulation - genetics</subject><issn>0378-1119</issn><issn>1879-0038</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kElPwzAQhS0EomX5AxyQj1wSvMSJLXFBiE0UIbGcLdeetK6ygJ2A-Pe4FDgyl5Fm3jy9-RA6oiSnhJanq3wBHeSMUJUTlpOq2kJTKiuVEcLlNpoSXsmMUqomaC_GFUklBNtFE05koURBpujp3j9mUir8Gvq2HyBiC02DF6H_GJbYd3g5tqbDXd9lsTVp871uxm6BreksBDz_xAEWY2MGn4Z3syt1gHZq00Q4_On76OXq8vniJps9XN9enM8yy0U5ZM4QoUAxJhwvaqoMK1lRg5uXpTNz6wohReVqySlYxgwnVPJSllxJaUEqzvfRycY3ZX8bIQ669XGdz3TQj1EzKtOTkpYiSdlGakMfY4BavwbfmvCpKdFrmHql1zD1GqYmTCeY6ej4x3-ct-D-Tn7pJcHZRgDpy3cPQUfrIVFxPoAdtOv9f_5f9xWD3w</recordid><startdate>20190530</startdate><enddate>20190530</enddate><creator>Han, Xu</creator><creator>Tang, Yihu</creator><creator>Dai, Yawei</creator><creator>Hu, Shuai</creator><creator>Zhou, Jingxin</creator><creator>Liu, Xiang</creator><creator>Zhu, Jinfu</creator><creator>Wu, Yanhu</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20190530</creationdate><title>MiR-889 promotes cell growth in human non-small cell lung cancer by regulating KLF9</title><author>Han, Xu ; Tang, Yihu ; Dai, Yawei ; Hu, Shuai ; Zhou, Jingxin ; Liu, Xiang ; Zhu, Jinfu ; Wu, Yanhu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-da059e9225d34f19a2624fedb66dabcd45857df831ec22a301836863988ce8933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>A549 Cells</topic><topic>Carcinoma, Non-Small-Cell Lung - genetics</topic><topic>Cell Line, Tumor</topic><topic>Cell Movement - genetics</topic><topic>Cell Proliferation - genetics</topic><topic>Gene Expression Regulation, Neoplastic - genetics</topic><topic>Humans</topic><topic>KLF9</topic><topic>Kruppel-Like Transcription Factors - genetics</topic><topic>Lung Neoplasms - genetics</topic><topic>MicroRNAs - genetics</topic><topic>Migration</topic><topic>miR-889</topic><topic>NSCLC</topic><topic>Proliferation</topic><topic>Up-Regulation - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Han, Xu</creatorcontrib><creatorcontrib>Tang, Yihu</creatorcontrib><creatorcontrib>Dai, Yawei</creatorcontrib><creatorcontrib>Hu, Shuai</creatorcontrib><creatorcontrib>Zhou, Jingxin</creatorcontrib><creatorcontrib>Liu, Xiang</creatorcontrib><creatorcontrib>Zhu, Jinfu</creatorcontrib><creatorcontrib>Wu, Yanhu</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Gene</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Han, Xu</au><au>Tang, Yihu</au><au>Dai, Yawei</au><au>Hu, Shuai</au><au>Zhou, Jingxin</au><au>Liu, Xiang</au><au>Zhu, Jinfu</au><au>Wu, Yanhu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MiR-889 promotes cell growth in human non-small cell lung cancer by regulating KLF9</atitle><jtitle>Gene</jtitle><addtitle>Gene</addtitle><date>2019-05-30</date><risdate>2019</risdate><volume>699</volume><spage>94</spage><epage>101</epage><pages>94-101</pages><issn>0378-1119</issn><eissn>1879-0038</eissn><abstract>Currently, non-small cell lung cancer (NSCLC) is still the most common malignancy worldwide. 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Subsequently, knockdown of miR-889 significantly inhibited cell proliferation and migration, while overexpression of miR-889 had the opposite effect. KLF9 may be a potential target of miR-889. In addition, upregulation of miR-889 promotes tumorigenesis in vitro, and KLF9 protein levels are also reduced. The current study suggests that miR-889 may play a potential therapeutic role for NSCLC by targeting KLF9 to control NSCLC proliferation and migration. •miR-889 play an important role in NSCLC.•miR-889 promotes NSCLC cell proliferation and migration by regulating KLF9.•miR-889 may become a new targeted therapy for lung cancer.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>30849540</pmid><doi>10.1016/j.gene.2019.02.077</doi><tpages>8</tpages></addata></record>
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subjects A549 Cells
Carcinoma, Non-Small-Cell Lung - genetics
Cell Line, Tumor
Cell Movement - genetics
Cell Proliferation - genetics
Gene Expression Regulation, Neoplastic - genetics
Humans
KLF9
Kruppel-Like Transcription Factors - genetics
Lung Neoplasms - genetics
MicroRNAs - genetics
Migration
miR-889
NSCLC
Proliferation
Up-Regulation - genetics
title MiR-889 promotes cell growth in human non-small cell lung cancer by regulating KLF9
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