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Expression of neddylation-related proteins in melanoma cell lines and the effect of neddylation on melanoma proliferation

机译:黑色素瘤细胞系中与降息相关蛋白的表达及其对黑素瘤增殖的影响

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摘要

Neddylation promotes the process of ubiquitination, which plays a critical role in the degradation of numerous proteins, including cell cycle and apoptosis regulators. In our previous study, an increase in neddylation was identified in melanoma cell lines. In the present study, the upregulation of neddylation was detected in melanoma tissues which confirmed the results of our previous study on melanoma cell lines. To explore the mechanism by which the process of neddylation was increased, the enzymes that regulate the process were investigated. These neddylation-related regulatory enzymes are potential targets for melanoma therapy. Downregulation of UBA3, a subunit of the E1 enzyme, by RNA interference caused cell cycle arrest at G0/G1 in the M14 cell line. In addition, cyclin D expression declined, whereas p27, p21 and bax expression increased. These findings suggest that interfering with the neddylation pathway may decrease the proliferation of melanoma through the modulation of cell cycle regulators and apoptosis promoters.
机译:Neddylation促进泛素化的过程,泛素化在许多蛋白质的降解中起关键作用,包括细胞周期和凋亡调节剂。在我们先前的研究中,发现黑色素瘤细胞系中的联结作用增加。在本研究中,在黑色素瘤组织中检测到神经联蛋白的上调,这证实了我们先前关于黑色素瘤细胞系的研究结果。为了探索增加烯丙基化过程的机制,研究了调节该过程的酶。这些与神经元化有关的调节酶是黑色素瘤治疗的潜在靶标。 RNA干扰对E1酶亚基UBA3的下调导致细胞周期停滞在M14细胞系的G0 / G1处。此外,细胞周期蛋白D表达下降,而p27,p21和bax表达增加。这些发现提示,通过调节细胞周期调节剂和细胞凋亡启动子,干扰神经交联途径可减少黑色素瘤的增殖。

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