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MicroRNA alterations in head and neck squamous cell carcinoma

โœ Scribed by Steven S. Chang; Wei Wen Jiang; Ian Smith; Luana M. Poeta; Shahnaz Begum; Chad Glazer; Shannon Shan; William Westra; David Sidransky; Joseph A. Califano


Publisher
John Wiley and Sons
Year
2008
Tongue
French
Weight
244 KB
Volume
123
Category
Article
ISSN
0020-7136

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โœฆ Synopsis


Abstract

MicroRNAs (mirs) are small noncoding RNA molecules (โˆผ22 nucleotides) that regulate posttranscriptional gene expression. Currently, there has not been a comprehensive study of their role in primary head and neck squamous cell carcinoma (HNSCC). To determine the role of mirs in HNSCC, we screened for altered microRNA expression in HNSCC primary tissue and cell lines. We then further tested the functional impact of alterations of specific mirs. An initial screening of 4 primary HNSCC, 4 normal mucosal controls and 4 HNSCC cell lines was analyzed for mature microRNA expression by microarray. Significance was determined using significance analysis of microarrays (SAM). Nine microRNAs were found by SAM to be upregulated or downregulated in tumor tissue including mirโ€21, letโ€7, 18, 29c, 142โ€3p, 155, 146b (overexpressed) and 494 (underexpressed). Mirโ€21 was validated by qRTโ€PCR. Functional validation by growth assays was performed, further validating mirโ€21. Transfection of mirโ€21 into JHUโ€011 and JHUโ€012 cell lines showed a 39% increase in cell growth at 72 hr relative to controls (p < 0.05). Transfection of the inhibitor into JHUโ€O12 cell lines showed a 92% decrease in cell growth relative to controls at 72 hr (p < 0.05). In addition, flow cytometry analysis of JHUโ€012 cells 48 hr after mirโ€21 inhibitor transfection showed a statistically significant increase in cytochrome c release and increased apoptosis. These differentially expressed microRNAs may be of interest as potential novel oncogenes and tumor suppressor genes in HNSCC. Mirโ€21 is a putative oncogenic microRNA in head and neck cancer. ยฉ 2008 Wileyโ€Liss, Inc.


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