Title of article :
Down-regulation in human cancers of DRHC, a novel helicase-like gene from 17q25.1 that inhibits cell growth
Author/Authors :
Nagai، نويسنده , , H. and Yabe، نويسنده , , A. and Mine، نويسنده , , N. and Mikami، نويسنده , , I. and Fujiwara، نويسنده , , H. and Terada، نويسنده , , Y. and Hirano، نويسنده , , A. and Tsuneizumi، نويسنده , , M. and Yokota، نويسنده , , T. and Emi، نويسنده , , M.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2003
Pages :
7
From page :
41
To page :
47
Abstract :
Frequent observations of allelic loss in chromosomal band 17q25.1 in a variety of human cancers have suggested that one or more tumor suppressor genes are normally present in this region. Moreover, a locus responsible for hereditary focal non-epidermolytic palmoplantar keratoderma (tylosis oesophageal cancer; TOC), a condition associated with esophageal cancer, has been mapped to the same band. During efforts to sequence, by shot-gun methods, a 1 Mb target region that we had defined as the DNA segment harboring the putative tumor suppressor gene(s) involved in these events, we identified a novel cDNA, DRHC (down-regulated in human cancers), that showed reduced expression in 28 of 95 (29%) cell lines derived from a variety of human cancers. The full-length cDNA, 6275 bp long, was expressed predominantly in thymus and brain. The predicted 1942-amino-acid product exhibited significant sequence homology to yeast enzymes belonging to the DEAD-helicase superfamily, and appeared to be a Uvr/Rep helicase with a DEXDc consensus domain. Transfection of a DRHC expression vector inhibited growth of cancer cells in liquid medium or soft agar. The results suggest that loss of expression of DRHC may play a role in human carcinogenesis.
Keywords :
Tumor suppressor gene , Chromosome 17q , Loss of Heterozygosity , Tylosis with oesophageal cancer , helicase
Journal title :
Cancer Letters
Serial Year :
2003
Journal title :
Cancer Letters
Record number :
1804940
Link To Document :
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