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A Novel Role of Dickkopf-Related Protein 3 in Macropinocytosis in Human Bladder Cancer T24 Cells

机译:Dickkopf相关蛋白3在人膀胱癌T24细胞巨细胞增多中的新作用

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摘要

Dickkopf-related protein 3 (Dkk-3) is a potential tumor suppressor reported in various cancer entities. However, we found that Dkk-3 was exceptionally upregulated in bladder cancer T24 cells. To validate the biological role of Dkk-3 other than a tumor suppressor, we examined the function of Dkk-3 in T24 cells. Gene silencing of Dkk-3 inhibited cell growth through inducing G0/G1 cell-cycle arrest. Furthermore, Dkk-3 knock-down caused macropinocytosis accompanied by autophagy, which were canceled in part by their inhibitors 5-(N-ethyl-N-isopropyl) amiloride (EIPA) and 3-methyladenine (3-MA). The macropinocytosis was induced by the Dkk-3 knock-down when there were sufficient extracellular nutrients. On the other hand, when the nutritional condition was poor, the autophagy was mainly induced by the Dkk-3 knock-down. These data indicated that Dkk-3 has a role in modulating macropinocytotic and autophagic pathways, a distinct function other than a Wnt antagonist.
机译:Dickkopf相关蛋白3(Dkk-3)是在各种癌症实体中报道的潜在肿瘤抑制因子。但是,我们发现Dkk-3在膀胱癌T24细胞中异常上调。为了验证除肿瘤抑制因子以外的Dkk-3的生物学作用,我们检查了Dkk-3在T24细胞中的功能。 Dkk-3的基因沉默通过诱导G0 / G1细胞周期停滞来抑制细胞生长。此外,Dkk-3敲低引起巨噬细胞增多并伴有自噬,其吞噬作用部分被其抑制剂5-(N-乙基-N-异丙基)阿米洛利(EIPA)和3-甲基腺嘌呤(3-MA)抵消。当有足够的细胞外营养时,Dkk-3敲低可诱导巨胞吞作用。另一方面,当营养条件差时,自噬主要由Dkk-3敲除诱导。这些数据表明,Dkk-3在调节巨噬细胞和自噬途径中具有作用,这是Wnt拮抗剂以外的独特功能。

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