pubmed-article:18596939 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:18596939 | lifeskim:mentions | umls-concept:C0302592 | lld:lifeskim |
pubmed-article:18596939 | lifeskim:mentions | umls-concept:C1101610 | lld:lifeskim |
pubmed-article:18596939 | lifeskim:mentions | umls-concept:C1516170 | lld:lifeskim |
pubmed-article:18596939 | lifeskim:mentions | umls-concept:C0017262 | lld:lifeskim |
pubmed-article:18596939 | lifeskim:mentions | umls-concept:C1546857 | lld:lifeskim |
pubmed-article:18596939 | lifeskim:mentions | umls-concept:C1556066 | lld:lifeskim |
pubmed-article:18596939 | lifeskim:mentions | umls-concept:C1619636 | lld:lifeskim |
pubmed-article:18596939 | lifeskim:mentions | umls-concept:C1514873 | lld:lifeskim |
pubmed-article:18596939 | lifeskim:mentions | umls-concept:C2911684 | lld:lifeskim |
pubmed-article:18596939 | lifeskim:mentions | umls-concept:C0185117 | lld:lifeskim |
pubmed-article:18596939 | pubmed:issue | 7 | lld:pubmed |
pubmed-article:18596939 | pubmed:dateCreated | 2008-7-3 | lld:pubmed |
pubmed-article:18596939 | pubmed:abstractText | MicroRNAs (miRNAs) play important roles in cancer development. By cloning and sequencing of a HPV16(+) CaSki cell small RNA library, we isolated 174 miRNAs (including the novel miR-193c) which could be grouped into 46 different miRNA species, with miR-21, miR-24, miR-27a, and miR-205 being most abundant. We chose for further study 10 miRNAs according to their cloning frequency and associated their levels in 10 cervical cancer- or cervical intraepithelial neoplasia-derived cell lines. No correlation was observed between their expression with the presence or absence of an integrated or episomal HPV genome. All cell lines examined contained no detectable miR-143 and miR-145. HPV-infected cell lines expressed a different set of miRNAs when grown in organotypic raft cultured as compared to monolayer cell culture, including expression of miR-143 and miR-145. This suggests a correlation between miRNA expression and tissue differentiation. Using miRNA array analyses for age-matched normal cervix and cervical cancer tissues, in combination with northern blot verification, we identified significantly deregulated miRNAs in cervical cancer tissues, with miR-126, miR-143, and miR-145 downregulation and miR-15b, miR-16, miR-146a, and miR-155 upregulation. Functional studies showed that both miR-143 and miR-145 are suppressive to cell growth. When introduced into cell lines, miR-146a was found to promote cell proliferation. Collectively, our data indicate that downregulation of miR-143 and miR-145 and upregulation of miR-146a play a role in cervical carcinogenesis. | lld:pubmed |
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pubmed-article:18596939 | pubmed:language | eng | lld:pubmed |
pubmed-article:18596939 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18596939 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:18596939 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18596939 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:18596939 | pubmed:issn | 1932-6203 | lld:pubmed |
pubmed-article:18596939 | pubmed:author | pubmed-author:RaderJanet... | lld:pubmed |
pubmed-article:18596939 | pubmed:author | pubmed-author:TangShuangS | lld:pubmed |
pubmed-article:18596939 | pubmed:author | pubmed-author:ZhengZhi-Ming... | lld:pubmed |
pubmed-article:18596939 | pubmed:author | pubmed-author:WangXiaohongX | lld:pubmed |