Expression of the zinc transporter ZnT4 is decreased in the progression from early prostate disease to invasive prostate cancer

被引:108
作者
Henshall, SM
Afar, DEH
Rasiah, KK
Horvath, LG
Gish, K
Caras, I
Ramakrishnan, V
Wong, M
Jeffry, U
Kench, JG
Quinn, DI
Turner, JJ
Delprado, W
Lee, CS
Golovsky, D
Brenner, PC
O'Neill, GF
Kooner, R
Stricker, PD
Grygiel, JJ
Mack, DH
Sutherland, RL
机构
[1] St Vincents Hosp, Garvan Inst Med Res, Canc Res Program, Darlinghurst, NSW 2010, Australia
[2] Eos Biotechnol, Genom Res, San Francisco, CA 94080 USA
[3] St Vincents Hosp, Dept Anat Pathol, Darlinghurst, NSW 2010, Australia
[4] Douglass Hanly Moir Pathol, N Ryde, NSW 2113, Australia
[5] Royal Prince Alfred Hosp, Dept Anat Pathol, Camperdown, NSW 2050, Australia
[6] Univ Sydney, Dept Pathol, Camperdown, NSW 2050, Australia
[7] St Vincents Hosp, Dept Urol, Darlinghurst, NSW 2010, Australia
[8] St Vincents Hosp, Dept Med Oncol, Darlinghurst, NSW 2010, Australia
基金
英国医学研究理事会;
关键词
ZnT4; prostate cancer; zinc transporter; oligonucleotide microarrray; hyperplasia;
D O I
10.1038/sj.onc.1206797
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
We have utilized oligonucleotide microarrays to identify novel genes of potential clinical and biological importance in prostate cancer. RNA from 74 prostate cancers and 164 normal body samples representing 40 different tissues were analysed using a customized Affymetrix GeneChip(R) oligonucleotide microarray representative of over 90% of the expressed human genome. The gene for the zinc transporter ZnT4 was one of several genes that displayed significantly higher expression in prostate cancer compared to normal tissues from other organs. A polyclonal antipeptide antibody was used to demonstrate ZnT4 expression in the epithelium of all 165 elements of benign and 326 elements of localized prostate cancers examined and in nine of 10 advanced prostate cancer specimens by immunohistochemistry. Interestingly, decreased intensity of ZnT4 immunoreactivity occurred in the progression from benign to invasive localized prostate cancer and to metastatic disease. Immunofluorescence analysis and surface biotinylation studies of cells expressing ZnT4 localised the protein to intracellular vesicles and to the plasma membrane. These findings are consistent with a role for ZnT4 in vesicular transport of zinc to the cell membrane and potentially in efflux of zinc in the prostate.
引用
收藏
页码:6005 / 6012
页数:8
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