A novel gene on human chromosome 2p24 is differentially expressed between androgen-dependent and androgen-independent prostate cancer cells

被引:10
作者
Chang, GTG
Steenbeek, M
Schippers, E
Blok, LJ
van Weerden, WM
van Alewijk, DCJG
Eussen, BHJ
van Steenbrugge, GJ
Brinkmann, AO
机构
[1] Erasmus Univ, Dept Endocrinol & Reprod, NL-3000 DR Rotterdam, Netherlands
[2] Erasmus Univ, Josephine Nefkens Inst, Dept Expt Urol, NL-3000 DR Rotterdam, Netherlands
[3] Erasmus Univ, Josephine Nefkens Inst, Dept Expt Pathol, NL-3000 DR Rotterdam, Netherlands
[4] Erasmus Univ, Dept Clin Genet, NL-3000 DR Rotterdam, Netherlands
关键词
differential gene expression; androgen-independent; prostate cancer; chromosome; 2p24;
D O I
10.1016/S0959-8049(01)00259-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Identification of genes involved in the transition from androgen-dependent to androgen-independent prostate cancer is important to extend our current knowledge of the disease. Using differential display RT-PCR analysis between androgen-dependent and androgen-independent prostate cancer cells, we have identified a novel gene, designated GC109. GC109 harbours a putative Cys-His cluster, a nuclear localisation signal, a leucine zipper and a ret finger protein (rfp)-like domain. GC109 mRNA expression in normal human tissues was found not to be restricted to the prostate. However, using a variety of 15 human cancer cell lines, GC109 mRNA was preferentially expressed in androgen-dependent LNCaP-FGC, compared with androgen-independent LNCaP-LNO, DU145 and PC3 human prostate cancer cells. Finally, the GC109 gene was mapped on human chromosome 2p24. Based on its protein domain structure and chromosomal localisation, we hypothesise that GC109 may be involved in chromosomal rearrangements in prostate cancer. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2129 / 2134
页数:6
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