Source:http://linkedlifedata.com/resource/pubmed/id/20484038
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
2010-6-2
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pubmed:abstractText |
EBV-associated gastric carcinoma is a distinct gastric carcinoma subtype with characteristic morphologic features similar to those of cells that undergo epithelial-to-mesenchymal transition. The effect of microRNA abnormalities in carcinogenesis was investigated by measuring the expression of the epithelial-to-mesenchymal transition-related microRNAs, miR-200a and miR-200b, in 36 surgically resected gastric carcinomas using quantitative reverse transcription-PCR analysis. MiR-200 family expression was decreased in EBV-associated gastric carcinoma, as compared with that in EBV-negative carcinoma. Downregulation of the miR-200 family was found in gastric carcinoma cell lines infected with recombinant EBV (MKN74-EBV, MKN7-EBV, and NUGC3-EBV), accompanied by the loss of cell adhesion, reduction of E-cadherin expression, and upregulation of ZEB1 and ZEB2. E-cadherin expression was partially restored by transfection of EBV-infected cells with miR-200 family precursors. Reverse transcription-PCR analysis of primary precursors of miR-200 (pri-miR-200) revealed that the transcription of pri-miR-200 was decreased in EBV-infected cells. Transfection of MKN74 cells with BARF0, EBNA1, and LMP2A resulted in a decrease of pri-miR-200, whereas transfection with EBV-encoded small RNA (EBER) did not. These four latent genes contributed to the downregulation of the mature miR-200 family and the subsequent upregulation of ZEB1/ZEB2, resulting in the reduction of E-cadherin expression. These findings indicate that all the latency type I genes have a synergetic effect on the downregulation of the miR-200 family that leads to reduced E-cadherin expression, which is a crucial step in the carcinogenesis of EBV-associated gastric carcinoma.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1538-7445
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pubmed:author | |
pubmed:copyrightInfo |
Copyright 2010 AACR.
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pubmed:issnType |
Electronic
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pubmed:day |
1
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pubmed:volume |
70
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4719-27
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pubmed:meshHeading |
pubmed-meshheading:20484038-Cadherins,
pubmed-meshheading:20484038-Cell Line, Tumor,
pubmed-meshheading:20484038-Down-Regulation,
pubmed-meshheading:20484038-Epstein-Barr Virus Infections,
pubmed-meshheading:20484038-Gene Expression Regulation, Neoplastic,
pubmed-meshheading:20484038-Gene Expression Regulation, Viral,
pubmed-meshheading:20484038-Herpesvirus 4, Human,
pubmed-meshheading:20484038-Humans,
pubmed-meshheading:20484038-MicroRNAs,
pubmed-meshheading:20484038-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:20484038-Stomach Neoplasms,
pubmed-meshheading:20484038-Transfection,
pubmed-meshheading:20484038-Virus Latency
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pubmed:year |
2010
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pubmed:articleTitle |
Downregulation of microRNA-200 in EBV-associated gastric carcinoma.
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pubmed:affiliation |
Department of Pathology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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