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靶向泛素E3连接酶RNF5作为神经外胚层肿瘤的一种新型治疗策略。

Targeting of Ubiquitin E3 Ligase RNF5 as a Novel Therapeutic Strategy in Neuroectodermal Tumors.

作者信息

Principi Elisa, Sondo Elvira, Bianchi Giovanna, Ravera Silvia, Morini Martina, Tomati Valeria, Pastorino Cristina, Zara Federico, Bruno Claudio, Eva Alessandra, Pedemonte Nicoletta, Raffaghello Lizzia

机构信息

Center of Translational and Experimental Myology, IRCCS Istituto Giannina Gaslini, 16147 Genoa, Italy.

UOC Genetica Medica, IRCCS Istituto Giannina Gaslini, 16147 Genoa, Italy.

出版信息

Cancers (Basel). 2022 Apr 1;14(7):1802. doi: 10.3390/cancers14071802.

DOI:10.3390/cancers14071802
PMID:35406574
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8997491/
Abstract

RNF5, an endoplasmic reticulum (ER) E3 ubiquitin ligase, participates to the ER-associated protein degradation guaranteeing the protein homeostasis. Depending on tumor model tested, RNF5 exerts pro- or anti-tumor activity. The aim of this study was to elucidate the controversial role of RNF5 in neuroblastoma and melanoma, two neuroectodermal tumors of infancy and adulthood, respectively. RNF5 gene levels are evaluated in publicly available datasets reporting the gene expression profile of melanoma and neuroblastoma primary tumors at diagnosis. The therapeutic effect of Analog-1, an RNF5 pharmacological activator, was investigated on in vitro and in vivo neuroblastoma and melanoma models. In both neuroblastoma and melanoma patients the high expression of RNF5 correlated with a better prognostic outcome. Treatment of neuroblastoma and melanoma cell lines with Analog-1 reduced cell viability by impairing the glutamine availability and energy metabolism through inhibition of FF ATP-synthase activity. This latter event led to a marked increase in oxidative stress, which, in turn, caused cell death. Similarly, neuroblastoma- and melanoma-bearing mice treated with Analog-1 showed a significant delay of tumor growth in comparison to those treated with vehicle only. These findings validate RNF5 as an innovative drug target and support the development of Analog-1 in early phase clinical trials for neuroblastoma and melanoma patients.

摘要

RNF5是一种内质网(ER)E3泛素连接酶,参与内质网相关蛋白降解以确保蛋白质稳态。根据所测试的肿瘤模型,RNF5发挥促肿瘤或抗肿瘤活性。本研究的目的是阐明RNF5在神经母细胞瘤和黑色素瘤(分别为婴幼儿期和成年期的两种神经外胚层肿瘤)中存在争议的作用。在公开可用的数据集中评估了RNF5基因水平,这些数据集报告了黑色素瘤和神经母细胞瘤原发性肿瘤在诊断时的基因表达谱。研究了RNF5药理激活剂Analog-1对体外和体内神经母细胞瘤及黑色素瘤模型的治疗效果。在神经母细胞瘤和黑色素瘤患者中,RNF5的高表达均与较好的预后结果相关。用Analog-1处理神经母细胞瘤和黑色素瘤细胞系会通过抑制FF ATP合酶活性损害谷氨酰胺可用性和能量代谢,从而降低细胞活力。后一事件导致氧化应激显著增加,进而导致细胞死亡。同样,与仅用赋形剂处理的小鼠相比,用Analog-1处理的荷神经母细胞瘤和荷黑色素瘤小鼠的肿瘤生长明显延迟。这些发现证实RNF5是一个创新的药物靶点,并支持在神经母细胞瘤和黑色素瘤患者的早期临床试验中开发Analog-1。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50ba/8997491/93e0e817cb12/cancers-14-01802-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50ba/8997491/8eb414e2af3d/cancers-14-01802-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50ba/8997491/b2191a173a5b/cancers-14-01802-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50ba/8997491/6a6426dc8884/cancers-14-01802-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50ba/8997491/da6bdeb8bc9f/cancers-14-01802-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50ba/8997491/ac6e02c48f2b/cancers-14-01802-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50ba/8997491/93e0e817cb12/cancers-14-01802-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50ba/8997491/8eb414e2af3d/cancers-14-01802-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50ba/8997491/b2191a173a5b/cancers-14-01802-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50ba/8997491/6a6426dc8884/cancers-14-01802-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50ba/8997491/da6bdeb8bc9f/cancers-14-01802-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50ba/8997491/ac6e02c48f2b/cancers-14-01802-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50ba/8997491/93e0e817cb12/cancers-14-01802-g006.jpg

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