Aberrant promoter methylation and tumor suppressive activity of the DFNA5 gene in colorectal carcinoma

M. S. Kim, X. Chang, K. Yamashita, J. K. Nagpal, J. H. Baek, G. Wu, B. Trink, E. A. Ratovitski, Masaki Mori, D. Sidransky

研究成果: Contribution to journalArticle査読

67 被引用数 (Scopus)

抄録

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.

本文言語英語
ページ(範囲)3624-3634
ページ数11
ジャーナルOncogene
27
25
DOI
出版ステータス出版済み - 6 5 2008

All Science Journal Classification (ASJC) codes

  • Molecular Biology
  • Genetics
  • Cancer Research

フィンガープリント 「Aberrant promoter methylation and tumor suppressive activity of the DFNA5 gene in colorectal carcinoma」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

引用スタイル