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Impaired PIASy-Tip60 signaling weakens activation of p53 in melanoma

机译:PIASy-Tip60信号传导受损会削弱黑色素瘤中p53的激活

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摘要

The tumor suppressor p53 plays a central role in preventing tumor development by promoting transcription of genes that stall cell cycle and induce cell death. Although the majority of melanomas express wild-type p53, the molecular mechanisms that impede its activation remain unclear. We previously reported that the SUMO E3 ligase PIASy and the histone acetyltransferase Tip60 signaling cascade promote p53-dependent autophagy and apoptosis. We hypothesized that impairment in this signaling attenuates p53, thus disabling its apoptotic function in melanoma. Here, we show that human melanoma patient samples and cell lines maintain p53 expression but PIASy and/or Tip60 are frequently lost. We observed dysregulation of Tip60-mediated p53 transcription program in melanoma cell lines. Reconstitution of PIASy and Tip60 in melanoma cells increased genotoxic stress-induced apoptosis. Our study provides a clinical link of how sumoylation signaling may activate p53-mediated cell death in melanoma.
机译:肿瘤抑制因子p53通过促进使细胞周期停滞并诱导细胞死亡的基因转录,在预防肿瘤发展中发挥重要作用。尽管大多数黑色素瘤表达野生型p53,但阻碍其激活的分子机制仍不清楚。我们以前曾报道过SUMO E3连接酶PIASy和组蛋白乙酰转移酶Tip60信号级联促进p53依赖的自噬和细胞凋亡。我们假设该信号转导通路的损伤会减弱p53,从而使其在黑素瘤中的凋亡功能失效。在这里,我们显示人类黑素瘤患者样品和细胞系保持p53表达,但PIASy和/或Tip60经常丢失。我们观察到黑色素瘤细胞系中Tip60介导的p53转录程序的失调。黑色素瘤细胞中PIASy和Tip60的重建增加了遗传毒性应激诱导的细胞凋亡。我们的研究提供了一个临床联系,说明磺酰化信号传导如何激活黑色素瘤中p53介导的细胞死亡。

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