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首页> 外文期刊>Molecular medicine reports >MicroRNA-328 directly targets p21-activated protein kinase 6 inhibiting prostate cancer proliferation and enhancing docetaxel sensitivity
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MicroRNA-328 directly targets p21-activated protein kinase 6 inhibiting prostate cancer proliferation and enhancing docetaxel sensitivity

机译:MicroRNA-328直接靶向p21激活的蛋白激酶6抑制前列腺癌的增殖并增强多西他赛的敏感性

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Prostate cancer (Pca) has one of the highest mortality rates for malignant cancers worldwide. Previous research has demonstrated that numerous genes are aberrantly expressed during Pea onset and development, p21-activated protein kinase 6 (PAK6) is known to be overexpressed in primary and metastatic Pea, however the mechanism of this aberrant expression remains unknown. In the present study, immunohistochemistry demonstrated that PAK6 is overexpressed in castration-resistant Pea (CRPC). Furthermore, PAK6 overexpression was regulated by microRNA (miR)-328. Luciferase reporter assay and western blot analysis indicated that PAK6 was directly targeted by miR-328. Forced expression of miR-328 enhanced docetaxel sensitivity, inhibited cell proliferation and promoted cell apoptosis without affecting the cell cycle. This indicates that miR-328 performs important functions in CRPC progression via PAK6 regulation. This mechanism may be used to enhance the effect of docetaxel.
机译:前列腺癌(Pca)是全球恶性肿瘤死亡率最高的国家之一。先前的研究表明,在豌豆发病和发育过程中大量表达了异常基因,已知p21活化蛋白激酶6(PAK6)在豌豆的初级和转移性豌豆中过表达,但是这种异常表达的机制仍然未知。在本研究中,免疫组织化学证明PAK6在去势抵抗性豌豆(CRPC)中过表达。此外,PAK6的过表达受microRNA(miR)-328的调节。荧光素酶报告基因分析和蛋白质印迹分析表明,miR-328直接靶向PAK6。 miR-328的强制表达增强了多西紫杉醇的敏感性,抑制了细胞的增殖,并促进了细胞的凋亡而不影响细胞周期。这表明miR-328通过PAK6调控在CRPC进展中起重要作用。该机制可用于增强多西他赛的作用。

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