Quantification of expression of netrins, slits and their receptors in human prostate tumors

被引:122
作者
Latil, A
Chêne, L
Cochant-Priollet, B
Mangin, P
Fournier, G
Berthon, P
Cussenot, O
机构
[1] UroGene, Genopole, F-91058 Evry, France
[2] Fac Med, CeRePP EA 3104, Paris, France
[3] Univ Paris 07, Hop St Louis, Dept Urol, Paris, France
[4] Inst Univ France, Paris, France
[5] Hop Lariboisiere, F-75475 Paris, France
[6] Hop Brabois, Vandoeuvre Les Nancy, France
[7] Hop Cavale Blanche, Brest, France
关键词
human prostate cancer; real-time quantitative RT-PCR assay;
D O I
10.1002/ijc.10821
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recently, DCC (Deleted in Colorectal Cancer) protein has been forwarded as a receptor for netrin. The Netrin/DCC complex is critical for axon guidance and cell migration. In the developing nervous system, netrin protein secreted by midline cells attracts commissural axons by activating the DCC receptor on growth cones. This attraction can be switched to repulsion or silenced completely, depending on the DCC binding partner. The potential suppressor function of DCC in prostate tumorigenesis, through a still unknown mechanism, prompted us to quantify the expression of several genes involved in this axon guidance pathway. The relative expression levels of DCC, NEO1, NTN1, NTN2L, NTN4, UNC5C, Slit1, Slit2, Slit3, Robo1 and Robo2 were simultaneous quantified in 48 tumors and 7 normal prostate tissues by using real-time quantitative reverse transcriptase-polymerase chain reaction (RT-PCR), A reduction in DCC, NEO1, NTN1 and NTN4 expression was observed in prostate tumors, while many of the same prostate tumors over-expressed either Slit genes or their receptors, Robo. (C) 2002 Wiley-Liss, Inc.
引用
收藏
页码:306 / 315
页数:10
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