Over-Expression of miR-21 and Lower PTEN Levels in Wilms’ Tumor with Aggressive Behavior
Wilms’ tumor (WT) is the most common pediatric kidney tumor. MiR-21 is one of the most frequently overexpressed microRNAs in solid tumors, while phosphatase and tensin homolog deleted from chromosome 10 (PTEN) is the most highly mutated tumor suppressor gene. The aim of this study was to investigate...
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Veröffentlicht in: | The Tohoku Journal of Experimental Medicine 2017, Vol.242(1), pp.43-52 |
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description | Wilms’ tumor (WT) is the most common pediatric kidney tumor. MiR-21 is one of the most frequently overexpressed microRNAs in solid tumors, while phosphatase and tensin homolog deleted from chromosome 10 (PTEN) is the most highly mutated tumor suppressor gene. The aim of this study was to investigate the relationship between miR-21 and PTEN in WT. The expression levels of miR-21 and the PTEN protein were determined by qRT-PCR and Western blot analyses in WT specimens, respectively. In WT tissues, the miR-21 expression levels were significantly higher and the PTEN protein levels were significantly lower, compared to the adjacent non-tumorous renal tissues. The higher levels of miR-21 and lower levels of PTEN were correlated with age (> 24 months), late clinical stage, unfavorable histopathological type and lymphatic metastasis. A univariate linear regression analysis indicated a significant correlation between higher miR-21 levels and lower PTEN levels. Using the SK-NEP-1 WT cell line, we showed that the decreased expression levels of miR-21 promoted cell proliferation and invasion, but inhibited apoptosis. Importantly, lowered expression levels of miR-21 increased the expression levels of PTEN protein and decreased the expression levels of phosphoinositide 3-kinase (PI3K) and phosphorylated protein kinase B (p-AKT), each of which functions in the downstream signaling pathway. Dual luciferase-reporter assays indicated that PTEN mRNA was a direct target of miR-21. In conclusion, higher miR-21 levels and lower PTEN protein levels are predictive biomarkers for poor prognosis of WT patients. Over-expression of miR-21 promotes aggressive behavior of WT by targeting PTEN. |
doi_str_mv | 10.1620/tjem.242.43 |
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MiR-21 is one of the most frequently overexpressed microRNAs in solid tumors, while phosphatase and tensin homolog deleted from chromosome 10 (PTEN) is the most highly mutated tumor suppressor gene. The aim of this study was to investigate the relationship between miR-21 and PTEN in WT. The expression levels of miR-21 and the PTEN protein were determined by qRT-PCR and Western blot analyses in WT specimens, respectively. In WT tissues, the miR-21 expression levels were significantly higher and the PTEN protein levels were significantly lower, compared to the adjacent non-tumorous renal tissues. The higher levels of miR-21 and lower levels of PTEN were correlated with age (> 24 months), late clinical stage, unfavorable histopathological type and lymphatic metastasis. A univariate linear regression analysis indicated a significant correlation between higher miR-21 levels and lower PTEN levels. Using the SK-NEP-1 WT cell line, we showed that the decreased expression levels of miR-21 promoted cell proliferation and invasion, but inhibited apoptosis. Importantly, lowered expression levels of miR-21 increased the expression levels of PTEN protein and decreased the expression levels of phosphoinositide 3-kinase (PI3K) and phosphorylated protein kinase B (p-AKT), each of which functions in the downstream signaling pathway. Dual luciferase-reporter assays indicated that PTEN mRNA was a direct target of miR-21. In conclusion, higher miR-21 levels and lower PTEN protein levels are predictive biomarkers for poor prognosis of WT patients. Over-expression of miR-21 promotes aggressive behavior of WT by targeting PTEN.</description><identifier>ISSN: 0040-8727</identifier><identifier>EISSN: 1349-3329</identifier><identifier>DOI: 10.1620/tjem.242.43</identifier><identifier>PMID: 28529243</identifier><language>eng</language><publisher>Japan: Tohoku University Medical Press</publisher><subject>3' Untranslated Regions - genetics ; Adult ; Apoptosis - genetics ; Base Sequence ; Cell Line, Tumor ; Cell Proliferation ; Female ; Gene Expression Regulation, Neoplastic ; Humans ; Kidney Neoplasms - genetics ; Kidney Neoplasms - pathology ; Luciferases - metabolism ; Male ; MicroRNAs - genetics ; MicroRNAs - metabolism ; miR-21 ; Neoplasm Invasiveness ; Phosphatidylinositol 3-Kinases - metabolism ; Phosphorylation ; PTEN ; PTEN Phosphohydrolase - genetics ; PTEN Phosphohydrolase - metabolism ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; SK-NEP-1 cell ; target gene ; Transfection ; Wilms Tumor - genetics ; Wilms Tumor - pathology ; Wilms’ tumor ; Young Adult</subject><ispartof>The Tohoku Journal of Experimental Medicine, 2017, Vol.242(1), pp.43-52</ispartof><rights>2017 Tohoku University Medical Press</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c472t-5cb4cbdd1f25b6bf4a4cd52d18299d53331defbb61028d8850f8c4f8daf4b77b3</citedby><cites>FETCH-LOGICAL-c472t-5cb4cbdd1f25b6bf4a4cd52d18299d53331defbb61028d8850f8c4f8daf4b77b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1877,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28529243$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cui, Mingyu</creatorcontrib><creatorcontrib>Liu, Wei</creatorcontrib><creatorcontrib>Zhang, Lijuan</creatorcontrib><creatorcontrib>Guo, Feng</creatorcontrib><creatorcontrib>Liu, Yang</creatorcontrib><creatorcontrib>Chen, Fang</creatorcontrib><creatorcontrib>Liu, Ting</creatorcontrib><creatorcontrib>Ma, Rui</creatorcontrib><creatorcontrib>Wu, Rongde</creatorcontrib><title>Over-Expression of miR-21 and Lower PTEN Levels in Wilms’ Tumor with Aggressive Behavior</title><title>The Tohoku Journal of Experimental Medicine</title><addtitle>Tohoku J. Exp. Med.</addtitle><description>Wilms’ tumor (WT) is the most common pediatric kidney tumor. MiR-21 is one of the most frequently overexpressed microRNAs in solid tumors, while phosphatase and tensin homolog deleted from chromosome 10 (PTEN) is the most highly mutated tumor suppressor gene. The aim of this study was to investigate the relationship between miR-21 and PTEN in WT. The expression levels of miR-21 and the PTEN protein were determined by qRT-PCR and Western blot analyses in WT specimens, respectively. In WT tissues, the miR-21 expression levels were significantly higher and the PTEN protein levels were significantly lower, compared to the adjacent non-tumorous renal tissues. The higher levels of miR-21 and lower levels of PTEN were correlated with age (> 24 months), late clinical stage, unfavorable histopathological type and lymphatic metastasis. A univariate linear regression analysis indicated a significant correlation between higher miR-21 levels and lower PTEN levels. Using the SK-NEP-1 WT cell line, we showed that the decreased expression levels of miR-21 promoted cell proliferation and invasion, but inhibited apoptosis. Importantly, lowered expression levels of miR-21 increased the expression levels of PTEN protein and decreased the expression levels of phosphoinositide 3-kinase (PI3K) and phosphorylated protein kinase B (p-AKT), each of which functions in the downstream signaling pathway. Dual luciferase-reporter assays indicated that PTEN mRNA was a direct target of miR-21. In conclusion, higher miR-21 levels and lower PTEN protein levels are predictive biomarkers for poor prognosis of WT patients. Over-expression of miR-21 promotes aggressive behavior of WT by targeting PTEN.</description><subject>3' Untranslated Regions - genetics</subject><subject>Adult</subject><subject>Apoptosis - genetics</subject><subject>Base Sequence</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation</subject><subject>Female</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Humans</subject><subject>Kidney Neoplasms - genetics</subject><subject>Kidney Neoplasms - pathology</subject><subject>Luciferases - metabolism</subject><subject>Male</subject><subject>MicroRNAs - genetics</subject><subject>MicroRNAs - metabolism</subject><subject>miR-21</subject><subject>Neoplasm Invasiveness</subject><subject>Phosphatidylinositol 3-Kinases - metabolism</subject><subject>Phosphorylation</subject><subject>PTEN</subject><subject>PTEN Phosphohydrolase - genetics</subject><subject>PTEN Phosphohydrolase - metabolism</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>SK-NEP-1 cell</subject><subject>target gene</subject><subject>Transfection</subject><subject>Wilms Tumor - genetics</subject><subject>Wilms Tumor - pathology</subject><subject>Wilms’ tumor</subject><subject>Young Adult</subject><issn>0040-8727</issn><issn>1349-3329</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpF0MtOGzEUxnGrKirhsuq-8rISmuDbZDyriqJQKkUEoSAkNpYvx4mjuaT2JMCO1-jr8SRNSEhXZ3F--i8-hL5S0qcDRs67OdR9Jlhf8E-oR7koM85Z-Rn1CBEkkwUrDtFRSnNCuCDF4As6ZDJnJRO8hx7HK4jZ8HkRIaXQNrj1uA53GaNYNw6P2ieI-HYyvMEjWEGVcGjwQ6jq9Pb6F0-WdRvxU-hm-GI6fS-sAP-EmV6FNp6gA6-rBKe7e4zur4aTy-tsNP71-_JilFlRsC7LrRHWOEc9y83AeKGFdTlzVLKydDnnnDrwxgwoYdJJmRMvrfDSaS9MURh-jL5vu4vY_llC6lQdkoWq0g20y6RoSSgnZZ7LNT3bUhvblCJ4tYih1vFFUaI2Y6rNmGo9phJ8rb_twktTg9vbj_XW4McWzFOnp7AHOnbBVvA_RnfJ_cfOdFTQ8H-J0Yey</recordid><startdate>20170501</startdate><enddate>20170501</enddate><creator>Cui, Mingyu</creator><creator>Liu, Wei</creator><creator>Zhang, Lijuan</creator><creator>Guo, Feng</creator><creator>Liu, Yang</creator><creator>Chen, Fang</creator><creator>Liu, Ting</creator><creator>Ma, Rui</creator><creator>Wu, Rongde</creator><general>Tohoku University Medical Press</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>20170501</creationdate><title>Over-Expression of miR-21 and Lower PTEN Levels in Wilms’ Tumor with Aggressive Behavior</title><author>Cui, Mingyu ; Liu, Wei ; Zhang, Lijuan ; Guo, Feng ; Liu, Yang ; Chen, Fang ; Liu, Ting ; Ma, Rui ; Wu, Rongde</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c472t-5cb4cbdd1f25b6bf4a4cd52d18299d53331defbb61028d8850f8c4f8daf4b77b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>3' Untranslated Regions - genetics</topic><topic>Adult</topic><topic>Apoptosis - genetics</topic><topic>Base Sequence</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation</topic><topic>Female</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Humans</topic><topic>Kidney Neoplasms - genetics</topic><topic>Kidney Neoplasms - pathology</topic><topic>Luciferases - metabolism</topic><topic>Male</topic><topic>MicroRNAs - genetics</topic><topic>MicroRNAs - metabolism</topic><topic>miR-21</topic><topic>Neoplasm Invasiveness</topic><topic>Phosphatidylinositol 3-Kinases - metabolism</topic><topic>Phosphorylation</topic><topic>PTEN</topic><topic>PTEN Phosphohydrolase - genetics</topic><topic>PTEN Phosphohydrolase - metabolism</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>SK-NEP-1 cell</topic><topic>target gene</topic><topic>Transfection</topic><topic>Wilms Tumor - genetics</topic><topic>Wilms Tumor - pathology</topic><topic>Wilms’ tumor</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cui, Mingyu</creatorcontrib><creatorcontrib>Liu, Wei</creatorcontrib><creatorcontrib>Zhang, Lijuan</creatorcontrib><creatorcontrib>Guo, Feng</creatorcontrib><creatorcontrib>Liu, Yang</creatorcontrib><creatorcontrib>Chen, Fang</creatorcontrib><creatorcontrib>Liu, Ting</creatorcontrib><creatorcontrib>Ma, Rui</creatorcontrib><creatorcontrib>Wu, Rongde</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>The Tohoku Journal of Experimental Medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cui, Mingyu</au><au>Liu, Wei</au><au>Zhang, Lijuan</au><au>Guo, Feng</au><au>Liu, Yang</au><au>Chen, Fang</au><au>Liu, Ting</au><au>Ma, Rui</au><au>Wu, Rongde</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Over-Expression of miR-21 and Lower PTEN Levels in Wilms’ Tumor with Aggressive Behavior</atitle><jtitle>The Tohoku Journal of Experimental Medicine</jtitle><addtitle>Tohoku J. Exp. Med.</addtitle><date>2017-05-01</date><risdate>2017</risdate><volume>242</volume><issue>1</issue><spage>43</spage><epage>52</epage><pages>43-52</pages><issn>0040-8727</issn><eissn>1349-3329</eissn><abstract>Wilms’ tumor (WT) is the most common pediatric kidney tumor. MiR-21 is one of the most frequently overexpressed microRNAs in solid tumors, while phosphatase and tensin homolog deleted from chromosome 10 (PTEN) is the most highly mutated tumor suppressor gene. The aim of this study was to investigate the relationship between miR-21 and PTEN in WT. The expression levels of miR-21 and the PTEN protein were determined by qRT-PCR and Western blot analyses in WT specimens, respectively. In WT tissues, the miR-21 expression levels were significantly higher and the PTEN protein levels were significantly lower, compared to the adjacent non-tumorous renal tissues. The higher levels of miR-21 and lower levels of PTEN were correlated with age (> 24 months), late clinical stage, unfavorable histopathological type and lymphatic metastasis. A univariate linear regression analysis indicated a significant correlation between higher miR-21 levels and lower PTEN levels. Using the SK-NEP-1 WT cell line, we showed that the decreased expression levels of miR-21 promoted cell proliferation and invasion, but inhibited apoptosis. Importantly, lowered expression levels of miR-21 increased the expression levels of PTEN protein and decreased the expression levels of phosphoinositide 3-kinase (PI3K) and phosphorylated protein kinase B (p-AKT), each of which functions in the downstream signaling pathway. Dual luciferase-reporter assays indicated that PTEN mRNA was a direct target of miR-21. In conclusion, higher miR-21 levels and lower PTEN protein levels are predictive biomarkers for poor prognosis of WT patients. Over-expression of miR-21 promotes aggressive behavior of WT by targeting PTEN.</abstract><cop>Japan</cop><pub>Tohoku University Medical Press</pub><pmid>28529243</pmid><doi>10.1620/tjem.242.43</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 3' Untranslated Regions - genetics Adult Apoptosis - genetics Base Sequence Cell Line, Tumor Cell Proliferation Female Gene Expression Regulation, Neoplastic Humans Kidney Neoplasms - genetics Kidney Neoplasms - pathology Luciferases - metabolism Male MicroRNAs - genetics MicroRNAs - metabolism miR-21 Neoplasm Invasiveness Phosphatidylinositol 3-Kinases - metabolism Phosphorylation PTEN PTEN Phosphohydrolase - genetics PTEN Phosphohydrolase - metabolism RNA, Messenger - genetics RNA, Messenger - metabolism SK-NEP-1 cell target gene Transfection Wilms Tumor - genetics Wilms Tumor - pathology Wilms’ tumor Young Adult |
title | Over-Expression of miR-21 and Lower PTEN Levels in Wilms’ Tumor with Aggressive Behavior |
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