前列腺Dickkopf-3功能:对上皮稳态和肿瘤进展的影响

Bioarchitecture Pub Date : 2013-03-01 DOI:10.4161/bioa.25243
Diana Romero, Robert Kypta
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引用次数: 12

摘要

肿瘤抑制因子Dickkopf-3 (Dkk-3)是一种非常独特的分子。虽然它与分泌型Wnt拮抗剂Dickkopf家族有关,但它并不直接抑制Wnt信号,其功能和作用机制尚不清楚。最近发现内源性Dkk-3在发育中的小鼠前列腺和人类前列腺上皮细胞的3D培养中都需要限制细胞增殖。Dkk-3进一步被证明可以调节正常前列腺上皮细胞对转化生长因子-β (TGF-β)的反应。这些研究与正常细胞需要Dkk-3来阻止TGF-β从肿瘤抑制因子转换为肿瘤启动子的模型一致。在这里,我们讨论这些发现及其对前列腺癌发生和发展的潜在影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dickkopf-3 function in the prostate: implications for epithelial homeostasis and tumor progression.

The tumor suppressor Dickkopf-3 (Dkk-3) is rather a unique molecule. Although it is related to the Dickkopf family of secreted Wnt antagonists, it does not directly inhibit Wnt signaling, and its function and mechanism of action are unknown. Endogenous Dkk-3 was recently found to be required to limit cell proliferation both in the developing mouse prostate and in 3D cultures of human prostate epithelial cells. Dkk-3 was further shown to modulate the response of normal prostate epithelial cells to transforming growth factor-β (TGF-β). These studies are consistent with a model in which Dkk-3 is required by normal cells to prevent the TGF-β switch from tumor suppressor to tumor promoter. Here, we discuss these findings and their potential impact on the development and progression of prostate cancer.

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