## Background: Squamous cell carcinoma (scc) of the head and neck region is rare in young patients and even less frequent in children 15 years or younger children. the patients reported in the literature are isolated cases and their management is always difficult because there is no large experienc
MicroRNA alterations in head and neck squamous cell carcinoma
โ 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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โฆ Synopsis
Abstract
MicroRNAs (mirs) are small noncoding RNA molecules (โผ22 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 mirโ21, letโ7, 18, 29c, 142โ3p, 155, 146b (overexpressed) and 494 (underexpressed). Mirโ21 was validated by qRTโPCR. Functional validation by growth assays was performed, further validating mirโ21. Transfection of mirโ21 into JHUโ011 and JHUโ012 cell lines showed a 39% increase in cell growth at 72 hr relative to controls (p < 0.05). Transfection of the inhibitor into JHUโO12 cell lines showed a 92% decrease in cell growth relative to controls at 72 hr (p < 0.05). In addition, flow cytometry analysis of JHUโ012 cells 48 hr after mirโ21 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. Mirโ21 is a putative oncogenic microRNA in head and neck cancer. ยฉ 2008 WileyโLiss, Inc.
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