Source:http://linkedlifedata.com/resource/pubmed/id/17892514
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
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pubmed:dateCreated |
2007-10-25
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pubmed:abstractText |
Recently, it has been found that inappropriate expression of microRNAs (miRNAs) is strongly associated with carcinogenesis. In this study, we demonstrated that the expression of miRNAs (miRs) -143 and -145, the levels of which were previously shown to be reduced in colon cancers and various kinds of established cancer cell lines, was also decreased in most of the B-cell malignancies examined, including chronic lymphocytic leukemias (CLL), B-cell lymphomas, Epstein-Barr virus (EBV)-transformed B-cell lines, and Burkitt lymphoma cell lines. All samples from 13 CLL patients and eight of nine B-cell lymphoma ones tested exhibited an extremely low expression of miRs-143 and -145. The expression levels of miRs-143 and -145 were consistently low in human Burkitt lymphoma cell lines and were inversely associated with the cell proliferation observed in the EBV-transformed B-cell lines. Moreover, the introduction of either precursor or mature miR-143 and -145 into Raji cells resulted in a significant growth inhibition that occurred in a dose-dependent manner and the target gene of miRNA-143 was determined to be ERK5, as previously reported in human colon cancer DLD-1 cells. Taken together, these findings suggest that miRs-143 and -145 may be useful as biomarkers that differentiate B-cell malignant cells from normal cells and contribute to carcinogenesis in B-cell malignancies by a newly defined mechanism.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antimetabolites, Antineoplastic,
http://linkedlifedata.com/resource/pubmed/chemical/Azacitidine,
http://linkedlifedata.com/resource/pubmed/chemical/Hydroxamic Acids,
http://linkedlifedata.com/resource/pubmed/chemical/MicroRNAs,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Neoplasm,
http://linkedlifedata.com/resource/pubmed/chemical/decitabine,
http://linkedlifedata.com/resource/pubmed/chemical/trichostatin A
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
1349-7006
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
98
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1914-20
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pubmed:meshHeading |
pubmed-meshheading:17892514-Antimetabolites, Antineoplastic,
pubmed-meshheading:17892514-Azacitidine,
pubmed-meshheading:17892514-Burkitt Lymphoma,
pubmed-meshheading:17892514-Cell Line, Tumor,
pubmed-meshheading:17892514-Cell Survival,
pubmed-meshheading:17892514-Down-Regulation,
pubmed-meshheading:17892514-Gene Expression Regulation, Neoplastic,
pubmed-meshheading:17892514-Humans,
pubmed-meshheading:17892514-Hydroxamic Acids,
pubmed-meshheading:17892514-Leukemia, Lymphocytic, Chronic, B-Cell,
pubmed-meshheading:17892514-Lymph Nodes,
pubmed-meshheading:17892514-Lymphoma, B-Cell,
pubmed-meshheading:17892514-MicroRNAs,
pubmed-meshheading:17892514-RNA, Neoplasm,
pubmed-meshheading:17892514-Tumor Cells, Cultured
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pubmed:year |
2007
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pubmed:articleTitle |
Downregulation of microRNAs-143 and -145 in B-cell malignancies.
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pubmed:affiliation |
Department of Medical Oncology, Gifu International Institute of Biotechnology, 1-1 Naka-Fudogaoka, Kakamigahara, Gifu 504-0838, Japan. yakao@giib.or.jp
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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