General information | Literature | Expression | Regulation | Mutation | Interaction |
Basic Information |
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Gene ID | 1687 |
Name | DFNA5 |
Synonymous | ICERE-1;deafness, autosomal dominant 5;DFNA5;deafness, autosomal dominant 5 |
Definition | inversely correlated with estrogen receptor expression 1|non-syndromic hearing impairment protein 5|nonsyndromic hearing impairment protein |
Position | 7p15 |
Gene type | protein-coding |
Title |
Abstract |
Aberrant promoter methylation and tumor suppressive activity of the DFNA5 gene in colorectal carcinoma. | To identify novel methylated gene promoters, we compared differential RNA expression profiles of colorectal cancer (CRC) cell lines with or without treatment of 5-aza-2-deoxycytidine (5-aza-dC). Out of 1776 genes that were initially absent (that is, silenced) by gene expression array analysis, we selected 163 genes that were increased after 5-aza-dC treatment in at least two of three CRC cell lines. The microarray results were confirmed by Reverse Transcription-PCR, and CpG island of the gene promoters were amplified and sequenced for examination of cancer-specific methylation. Among the genes identified, the deafness, autosomal dominant 5 gene, DFNA5, promoter was found to be methylated in primary tumor tissues with high frequency (65%, 65/100). Quantitative methylation-specific PCR of DFNA5 clearly discriminated primary CRC tissues from normal colon tissues (3%, 3/100). The mRNA expression of DFNA5 in four of five colon cancer tissues was significantly downregulated as compared to normal tissues. Moreover, forced expression of full-length DFNA5 in CRC cell lines markedly decreased the cell growth and colony-forming ability whereas knockdown of DFNA5 increased cell growth in culture. Our data implicate DFNA5 as a novel tumor suppressor gene in CRC and a valuable molecular marker for human cancer. |