WNT signalling in prostate cancer

被引:272
|
作者
Murillo-Garzon, Virginia [1 ]
Kypta, Robert [2 ]
机构
[1] CIC bioGUNE, Cell Biol & Stem Cells Unit, Bldg 801A,Bizkaia Technol Pk, Derio 48160, Spain
[2] Imperial Coll London, Dept Surg & Canc, Du Cane Rd, London W12 0NN, England
关键词
ANDROGEN RECEPTOR EXPRESSION; SMALL-MOLECULE INHIBITORS; BETA-CATENIN; WNT/BETA-CATENIN; GENE-EXPRESSION; IN-VIVO; BINDING PROTEIN; EMERGING ROLE; SELF-RENEWAL; TUMOR-GROWTH;
D O I
10.1038/nrurol.2017.144
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Genome sequencing and gene expression analyses of prostate tumours have highlighted the potential importance of genetic and epigenetic changes observed in WNT signalling pathway components in prostate tumours-particularly in the development of castration-resistant prostate cancer. WNT signalling is also important in the prostate tumour microenvironment, in which WNT proteins secreted by the tumour stroma promote resistance to therapy, and in prostate cancer stem or progenitor cells, in which WNT-beta-catenin signals promote self-renewal or expansion. Preclinical studies have demonstrated the potential of inhibitors that target WNT receptor complexes at the cell membrane or that block the interaction of beta-catenin with lymphoid enhancer-binding factor 1 and the androgen receptor, in preventing prostate cancer progression. Some WNT signalling inhibitors are in phase I trials, but they have yet to be tested in patients with prostate cancer.
引用
收藏
页码:683 / 696
页数:14
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