MicroRNA-191 promotes osteosarcoma cells proliferation by targeting checkpoint kinase 2
MicroRNAs (miRNAs) are small noncoding RNAs of 19–25 nt that can regulate gene expression at a posttranscriptional level. Increasing evidence indicates that miRNAs participate in almost every step of cellular processes and are often aberrantly expressed in human cancer. The aim of this study was to...
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Veröffentlicht in: | Tumor biology 2015-08, Vol.36 (8), p.6095-6101 |
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description | MicroRNAs (miRNAs) are small noncoding RNAs of 19–25 nt that can regulate gene expression at a posttranscriptional level. Increasing evidence indicates that miRNAs participate in almost every step of cellular processes and are often aberrantly expressed in human cancer. The aim of this study was to investigate the functional significance of miR-191 and to identify its possible target genes in osteosarcoma cells. Here, we found that the expression level of miR-191 was increased in osteosarcoma tissues in comparison with the adjacent normal tissues. The enforced expression of miR-191 was able to promote cell proliferation in Saos-2 and MG62 cells, while miR-191 antisense oligonucleotides blocked cell proliferation. At the molecular level, our results further revealed that expression of tumor suppressor gene, checkpoint kinase 2, was negatively regulated by miR-191. Therefore, we consider that miR-191 act as an onco-MicroRNA for osteosarcoma and it would offer a new way in molecular targeting cancer treatment. |
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Increasing evidence indicates that miRNAs participate in almost every step of cellular processes and are often aberrantly expressed in human cancer. The aim of this study was to investigate the functional significance of miR-191 and to identify its possible target genes in osteosarcoma cells. Here, we found that the expression level of miR-191 was increased in osteosarcoma tissues in comparison with the adjacent normal tissues. The enforced expression of miR-191 was able to promote cell proliferation in Saos-2 and MG62 cells, while miR-191 antisense oligonucleotides blocked cell proliferation. At the molecular level, our results further revealed that expression of tumor suppressor gene, checkpoint kinase 2, was negatively regulated by miR-191. Therefore, we consider that miR-191 act as an onco-MicroRNA for osteosarcoma and it would offer a new way in molecular targeting cancer treatment.</description><identifier>ISSN: 1010-4283</identifier><identifier>EISSN: 1423-0380</identifier><identifier>DOI: 10.1007/s13277-015-3290-9</identifier><identifier>PMID: 25773391</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Biomedical and Life Sciences ; Biomedicine ; Bone cancer ; Cancer Research ; Cell growth ; Cell Line, Tumor ; Cell Proliferation - genetics ; Checkpoint Kinase 2 - biosynthesis ; Checkpoint Kinase 2 - genetics ; Gene Expression Regulation, Neoplastic ; Humans ; Kinases ; MicroRNAs ; MicroRNAs - biosynthesis ; MicroRNAs - genetics ; MicroRNAs - metabolism ; Oligonucleotides, Antisense - genetics ; Osteosarcoma - genetics ; Osteosarcoma - pathology ; Protein expression ; Research Article</subject><ispartof>Tumor biology, 2015-08, Vol.36 (8), p.6095-6101</ispartof><rights>International Society of Oncology and BioMarkers (ISOBM) 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c405t-3d393e22203af13af603e5ae7a8f74b76e9af069cd515da97ff866228b00b0f93</citedby><cites>FETCH-LOGICAL-c405t-3d393e22203af13af603e5ae7a8f74b76e9af069cd515da97ff866228b00b0f93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s13277-015-3290-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s13277-015-3290-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25773391$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Huang, Ya-Zeng</creatorcontrib><creatorcontrib>Zhang, Jun</creatorcontrib><creatorcontrib>Shao, Hai-Yu</creatorcontrib><creatorcontrib>Chen, Jin-Ping</creatorcontrib><creatorcontrib>Zhao, Hong-Ying</creatorcontrib><title>MicroRNA-191 promotes osteosarcoma cells proliferation by targeting checkpoint kinase 2</title><title>Tumor biology</title><addtitle>Tumor Biol</addtitle><addtitle>Tumour Biol</addtitle><description>MicroRNAs (miRNAs) are small noncoding RNAs of 19–25 nt that can regulate gene expression at a posttranscriptional level. Increasing evidence indicates that miRNAs participate in almost every step of cellular processes and are often aberrantly expressed in human cancer. The aim of this study was to investigate the functional significance of miR-191 and to identify its possible target genes in osteosarcoma cells. Here, we found that the expression level of miR-191 was increased in osteosarcoma tissues in comparison with the adjacent normal tissues. The enforced expression of miR-191 was able to promote cell proliferation in Saos-2 and MG62 cells, while miR-191 antisense oligonucleotides blocked cell proliferation. At the molecular level, our results further revealed that expression of tumor suppressor gene, checkpoint kinase 2, was negatively regulated by miR-191. Therefore, we consider that miR-191 act as an onco-MicroRNA for osteosarcoma and it would offer a new way in molecular targeting cancer treatment.</description><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Bone cancer</subject><subject>Cancer Research</subject><subject>Cell growth</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation - genetics</subject><subject>Checkpoint Kinase 2 - biosynthesis</subject><subject>Checkpoint Kinase 2 - genetics</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Humans</subject><subject>Kinases</subject><subject>MicroRNAs</subject><subject>MicroRNAs - biosynthesis</subject><subject>MicroRNAs - genetics</subject><subject>MicroRNAs - metabolism</subject><subject>Oligonucleotides, Antisense - genetics</subject><subject>Osteosarcoma - genetics</subject><subject>Osteosarcoma - pathology</subject><subject>Protein expression</subject><subject>Research Article</subject><issn>1010-4283</issn><issn>1423-0380</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFkUtLxDAUhYMovn-AGym4cRO9SZqmWYr4glFBFJch7dyM1WkzJp3F_HtTZxQRxEVI4H45OTmHkAMGJwxAnUYmuFIUmKSCa6B6jWyznAsKooT1dAYGNOel2CI7Mb5CArUuNskWl0oJodk2eb5t6uAf7s4o0yybBd_6HmPmY48-2lD71mY1TqdxmE0bh8H2je-yapH1Nkywb7pJVr9g_TbzTddnb01nI2Z8j2w4O424v9p3ydPlxeP5NR3dX92cn41onYPsqRgLLZBzDsI6llYBAqVFZUun8koVqK2DQtdjyeTYauVcWRSclxVABU6LXXK81E323ucYe9M2cTBsO_TzaFgpda5kSuJ_VEEhVQm6TOjRL_TVz0OXPvJJAVMyLxLFllRKMMaAzsxC09qwMAzMUJBZFmRS7mYoyAx-D1fK86rF8feNr0YSwJdATKNuguHH03-qfgAJipm7</recordid><startdate>20150801</startdate><enddate>20150801</enddate><creator>Huang, Ya-Zeng</creator><creator>Zhang, Jun</creator><creator>Shao, Hai-Yu</creator><creator>Chen, Jin-Ping</creator><creator>Zhao, Hong-Ying</creator><general>Springer Netherlands</general><general>Springer Nature 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>3V.</scope><scope>7T5</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>7QP</scope></search><sort><creationdate>20150801</creationdate><title>MicroRNA-191 promotes osteosarcoma cells proliferation by targeting checkpoint kinase 2</title><author>Huang, Ya-Zeng ; Zhang, Jun ; Shao, Hai-Yu ; Chen, Jin-Ping ; Zhao, Hong-Ying</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c405t-3d393e22203af13af603e5ae7a8f74b76e9af069cd515da97ff866228b00b0f93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Bone cancer</topic><topic>Cancer Research</topic><topic>Cell growth</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation - genetics</topic><topic>Checkpoint Kinase 2 - biosynthesis</topic><topic>Checkpoint Kinase 2 - genetics</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Humans</topic><topic>Kinases</topic><topic>MicroRNAs</topic><topic>MicroRNAs - biosynthesis</topic><topic>MicroRNAs - genetics</topic><topic>MicroRNAs - metabolism</topic><topic>Oligonucleotides, Antisense - genetics</topic><topic>Osteosarcoma - genetics</topic><topic>Osteosarcoma - pathology</topic><topic>Protein expression</topic><topic>Research Article</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huang, Ya-Zeng</creatorcontrib><creatorcontrib>Zhang, Jun</creatorcontrib><creatorcontrib>Shao, Hai-Yu</creatorcontrib><creatorcontrib>Chen, Jin-Ping</creatorcontrib><creatorcontrib>Zhao, Hong-Ying</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>Calcium & Calcified Tissue Abstracts</collection><jtitle>Tumor biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huang, Ya-Zeng</au><au>Zhang, Jun</au><au>Shao, Hai-Yu</au><au>Chen, Jin-Ping</au><au>Zhao, Hong-Ying</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MicroRNA-191 promotes osteosarcoma cells proliferation by targeting checkpoint kinase 2</atitle><jtitle>Tumor biology</jtitle><stitle>Tumor Biol</stitle><addtitle>Tumour Biol</addtitle><date>2015-08-01</date><risdate>2015</risdate><volume>36</volume><issue>8</issue><spage>6095</spage><epage>6101</epage><pages>6095-6101</pages><issn>1010-4283</issn><eissn>1423-0380</eissn><abstract>MicroRNAs (miRNAs) are small noncoding RNAs of 19–25 nt that can regulate gene expression at a posttranscriptional level. Increasing evidence indicates that miRNAs participate in almost every step of cellular processes and are often aberrantly expressed in human cancer. The aim of this study was to investigate the functional significance of miR-191 and to identify its possible target genes in osteosarcoma cells. Here, we found that the expression level of miR-191 was increased in osteosarcoma tissues in comparison with the adjacent normal tissues. The enforced expression of miR-191 was able to promote cell proliferation in Saos-2 and MG62 cells, while miR-191 antisense oligonucleotides blocked cell proliferation. At the molecular level, our results further revealed that expression of tumor suppressor gene, checkpoint kinase 2, was negatively regulated by miR-191. Therefore, we consider that miR-191 act as an onco-MicroRNA for osteosarcoma and it would offer a new way in molecular targeting cancer treatment.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>25773391</pmid><doi>10.1007/s13277-015-3290-9</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biomedical and Life Sciences Biomedicine Bone cancer Cancer Research Cell growth Cell Line, Tumor Cell Proliferation - genetics Checkpoint Kinase 2 - biosynthesis Checkpoint Kinase 2 - genetics Gene Expression Regulation, Neoplastic Humans Kinases MicroRNAs MicroRNAs - biosynthesis MicroRNAs - genetics MicroRNAs - metabolism Oligonucleotides, Antisense - genetics Osteosarcoma - genetics Osteosarcoma - pathology Protein expression Research Article |
title | MicroRNA-191 promotes osteosarcoma cells proliferation by targeting checkpoint kinase 2 |
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