miR-140-5p alleviates the aggressive progression of Wilms' tumor through directly targeting TGFBRI gene

Background and objective: Although many miRNAs are identified to be deregulated and play vital roles in the progression of Wilms' tumor (WT), there are still a large number of miRNAs are waiting for us to explore. The purpose of the present study is to investigate the different expressing profi...

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Veröffentlicht in:Cancer management and research 2019-09, p.1641
Hauptverfasser: Wang, Hailei, Lou, Chunyan, Ma, Na
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Lou, Chunyan
Ma, Na
description Background and objective: Although many miRNAs are identified to be deregulated and play vital roles in the progression of Wilms' tumor (WT), there are still a large number of miRNAs are waiting for us to explore. The purpose of the present study is to investigate the different expressing profiles of miRNAs in WT tissues and the adjacent normal tissues, and probe the effects and mechanism of a certain miRNA among the different expressing miRNAs. Methods: miRNA microarray was recruited to assess the differently expressed miRNAs in WT tissues and normal tissues, which was further verified by RT-PCR. Receiver operating characteristic curves were performed to calculate the specificity and sensitivity of miRNAs in the diagnose of WT. CCK-8, flow cytometry, wound healing, transwell chamber and tumor-burdened assays were used to assess cell growth, apoptosis, migration, invasion and tumorigenesis. Luciferase report assay was used to evaluate the interaction between miR-140-5p and TGFBR1. Results: A total of 34 miRNAs were abnormally expressed in the WT tissues, among which, miR-140-5p was identified to be obviously down-regulated in WT tissues, and the AUC of it was 0.961. Besides, we found that patients with miR-140-5p low expression always had a shorter overall survival and more aggressive clinical features, such as bigger tumor size (P=0.002), higher pathological stage (P=0.003) and higher occurrence rate of lymph node metastasis (P=0.009) than those in patients with miR-140-5p high expression. Moreover, luciferase reporter assay showed that TGFBR1 was the direct target of miR-140-5p, which was negatively regulated by miR-140-5p and was highly expressed in WT tissues. Furthermore, knockdown of miR-140-5p obviously enhanced the proliferation and tumorigenesis and repressed the apoptosis of G401 cells, and these effects were all abolished when TGFBR1 was down-regulated. Conclusion: The present study illustrates that miR-140-5p functions as a tumor suppressor in the occurrence and development of WT via targeting TGFBR1, which provides theoretical foundation for serving miR-140-5p as a new diagnosis marker even a therapeutic target for WT. Keywords: miR-140-5p, TGFBR1, Wilms' tumor
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The purpose of the present study is to investigate the different expressing profiles of miRNAs in WT tissues and the adjacent normal tissues, and probe the effects and mechanism of a certain miRNA among the different expressing miRNAs. Methods: miRNA microarray was recruited to assess the differently expressed miRNAs in WT tissues and normal tissues, which was further verified by RT-PCR. Receiver operating characteristic curves were performed to calculate the specificity and sensitivity of miRNAs in the diagnose of WT. CCK-8, flow cytometry, wound healing, transwell chamber and tumor-burdened assays were used to assess cell growth, apoptosis, migration, invasion and tumorigenesis. Luciferase report assay was used to evaluate the interaction between miR-140-5p and TGFBR1. Results: A total of 34 miRNAs were abnormally expressed in the WT tissues, among which, miR-140-5p was identified to be obviously down-regulated in WT tissues, and the AUC of it was 0.961. Besides, we found that patients with miR-140-5p low expression always had a shorter overall survival and more aggressive clinical features, such as bigger tumor size (P=0.002), higher pathological stage (P=0.003) and higher occurrence rate of lymph node metastasis (P=0.009) than those in patients with miR-140-5p high expression. Moreover, luciferase reporter assay showed that TGFBR1 was the direct target of miR-140-5p, which was negatively regulated by miR-140-5p and was highly expressed in WT tissues. Furthermore, knockdown of miR-140-5p obviously enhanced the proliferation and tumorigenesis and repressed the apoptosis of G401 cells, and these effects were all abolished when TGFBR1 was down-regulated. Conclusion: The present study illustrates that miR-140-5p functions as a tumor suppressor in the occurrence and development of WT via targeting TGFBR1, which provides theoretical foundation for serving miR-140-5p as a new diagnosis marker even a therapeutic target for WT. Keywords: miR-140-5p, TGFBR1, Wilms' tumor</description><identifier>ISSN: 1179-1322</identifier><identifier>EISSN: 1179-1322</identifier><identifier>DOI: 10.2147/CMAR.S177508</identifier><language>eng</language><publisher>Dove Medical Press Limited</publisher><subject>Cancer metastasis ; Development and progression ; International economic relations ; Luciferase ; MicroRNA ; Scientific equipment industry ; Tumors ; Wound care ; Wound healing</subject><ispartof>Cancer management and research, 2019-09, p.1641</ispartof><rights>COPYRIGHT 2019 Dove Medical Press Limited</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,860,27903,27904</link.rule.ids></links><search><creatorcontrib>Wang, Hailei</creatorcontrib><creatorcontrib>Lou, Chunyan</creatorcontrib><creatorcontrib>Ma, Na</creatorcontrib><title>miR-140-5p alleviates the aggressive progression of Wilms' tumor through directly targeting TGFBRI gene</title><title>Cancer management and research</title><description>Background and objective: Although many miRNAs are identified to be deregulated and play vital roles in the progression of Wilms' tumor (WT), there are still a large number of miRNAs are waiting for us to explore. The purpose of the present study is to investigate the different expressing profiles of miRNAs in WT tissues and the adjacent normal tissues, and probe the effects and mechanism of a certain miRNA among the different expressing miRNAs. Methods: miRNA microarray was recruited to assess the differently expressed miRNAs in WT tissues and normal tissues, which was further verified by RT-PCR. Receiver operating characteristic curves were performed to calculate the specificity and sensitivity of miRNAs in the diagnose of WT. CCK-8, flow cytometry, wound healing, transwell chamber and tumor-burdened assays were used to assess cell growth, apoptosis, migration, invasion and tumorigenesis. Luciferase report assay was used to evaluate the interaction between miR-140-5p and TGFBR1. Results: A total of 34 miRNAs were abnormally expressed in the WT tissues, among which, miR-140-5p was identified to be obviously down-regulated in WT tissues, and the AUC of it was 0.961. Besides, we found that patients with miR-140-5p low expression always had a shorter overall survival and more aggressive clinical features, such as bigger tumor size (P=0.002), higher pathological stage (P=0.003) and higher occurrence rate of lymph node metastasis (P=0.009) than those in patients with miR-140-5p high expression. Moreover, luciferase reporter assay showed that TGFBR1 was the direct target of miR-140-5p, which was negatively regulated by miR-140-5p and was highly expressed in WT tissues. Furthermore, knockdown of miR-140-5p obviously enhanced the proliferation and tumorigenesis and repressed the apoptosis of G401 cells, and these effects were all abolished when TGFBR1 was down-regulated. Conclusion: The present study illustrates that miR-140-5p functions as a tumor suppressor in the occurrence and development of WT via targeting TGFBR1, which provides theoretical foundation for serving miR-140-5p as a new diagnosis marker even a therapeutic target for WT. Keywords: miR-140-5p, TGFBR1, Wilms' tumor</description><subject>Cancer metastasis</subject><subject>Development and progression</subject><subject>International economic relations</subject><subject>Luciferase</subject><subject>MicroRNA</subject><subject>Scientific equipment industry</subject><subject>Tumors</subject><subject>Wound care</subject><subject>Wound healing</subject><issn>1179-1322</issn><issn>1179-1322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNptj8FKAzEQhoMoWKs3HyDgwdPWZJPNbo612FqoCGvFY0mzkzSyuylJWvDtXaiHHmQO_8fPNwOD0D0lk5zy8mn2Nq0nH7QsC1JdoBGlpcwoy_PLM75GNzF-EyIkZXyEbOfqjHKSFXus2haOTiWIOO0AK2sDxOiOgPfBn9j32Bv85douPuJ06HwY1OAPdocbF0Cn9gcnFSwk11u8Xsyf6yW20MMtujKqjXD3l2P0OX9Zz16z1ftiOZuuMktZmTJRwFY3pqDGmHzLRKUUl9Q0mufbiggxfABEKCo1VIxQKAQxfLC1bhiXlWRj9HC6a1ULG9cbn4LSnYt6MxWE05JIxgdr8o81TAOd074H44b-bOEXlbhnyA</recordid><startdate>20190901</startdate><enddate>20190901</enddate><creator>Wang, Hailei</creator><creator>Lou, Chunyan</creator><creator>Ma, Na</creator><general>Dove Medical Press Limited</general><scope/></search><sort><creationdate>20190901</creationdate><title>miR-140-5p alleviates the aggressive progression of Wilms' tumor through directly targeting TGFBRI gene</title><author>Wang, Hailei ; Lou, Chunyan ; Ma, Na</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g137t-65ebcdf51fff2b368aa491fdc42b8066132e06a19ce8301e560f451fccd349893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Cancer metastasis</topic><topic>Development and progression</topic><topic>International economic relations</topic><topic>Luciferase</topic><topic>MicroRNA</topic><topic>Scientific equipment industry</topic><topic>Tumors</topic><topic>Wound care</topic><topic>Wound healing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Hailei</creatorcontrib><creatorcontrib>Lou, Chunyan</creatorcontrib><creatorcontrib>Ma, Na</creatorcontrib><jtitle>Cancer management and research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Hailei</au><au>Lou, Chunyan</au><au>Ma, Na</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>miR-140-5p alleviates the aggressive progression of Wilms' tumor through directly targeting TGFBRI gene</atitle><jtitle>Cancer management and research</jtitle><date>2019-09-01</date><risdate>2019</risdate><spage>1641</spage><pages>1641-</pages><issn>1179-1322</issn><eissn>1179-1322</eissn><abstract>Background and objective: Although many miRNAs are identified to be deregulated and play vital roles in the progression of Wilms' tumor (WT), there are still a large number of miRNAs are waiting for us to explore. The purpose of the present study is to investigate the different expressing profiles of miRNAs in WT tissues and the adjacent normal tissues, and probe the effects and mechanism of a certain miRNA among the different expressing miRNAs. Methods: miRNA microarray was recruited to assess the differently expressed miRNAs in WT tissues and normal tissues, which was further verified by RT-PCR. Receiver operating characteristic curves were performed to calculate the specificity and sensitivity of miRNAs in the diagnose of WT. CCK-8, flow cytometry, wound healing, transwell chamber and tumor-burdened assays were used to assess cell growth, apoptosis, migration, invasion and tumorigenesis. Luciferase report assay was used to evaluate the interaction between miR-140-5p and TGFBR1. Results: A total of 34 miRNAs were abnormally expressed in the WT tissues, among which, miR-140-5p was identified to be obviously down-regulated in WT tissues, and the AUC of it was 0.961. Besides, we found that patients with miR-140-5p low expression always had a shorter overall survival and more aggressive clinical features, such as bigger tumor size (P=0.002), higher pathological stage (P=0.003) and higher occurrence rate of lymph node metastasis (P=0.009) than those in patients with miR-140-5p high expression. Moreover, luciferase reporter assay showed that TGFBR1 was the direct target of miR-140-5p, which was negatively regulated by miR-140-5p and was highly expressed in WT tissues. Furthermore, knockdown of miR-140-5p obviously enhanced the proliferation and tumorigenesis and repressed the apoptosis of G401 cells, and these effects were all abolished when TGFBR1 was down-regulated. Conclusion: The present study illustrates that miR-140-5p functions as a tumor suppressor in the occurrence and development of WT via targeting TGFBR1, which provides theoretical foundation for serving miR-140-5p as a new diagnosis marker even a therapeutic target for WT. Keywords: miR-140-5p, TGFBR1, Wilms' tumor</abstract><pub>Dove Medical Press Limited</pub><doi>10.2147/CMAR.S177508</doi></addata></record>
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source Taylor & Francis Open Access; DOVE Medical Press Journals; DOAJ Directory of Open Access Journals; PubMed Central Open Access; EZB-FREE-00999 freely available EZB journals; PubMed Central
subjects Cancer metastasis
Development and progression
International economic relations
Luciferase
MicroRNA
Scientific equipment industry
Tumors
Wound care
Wound healing
title miR-140-5p alleviates the aggressive progression of Wilms' tumor through directly targeting TGFBRI gene
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