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蛋白质组学分析揭示了具有不同转移潜能的肝癌细胞系中不同的泛素化模式。

Proteomic analyses reveal divergent ubiquitylation patterns in hepatocellula carcinoma cell lines with different metastasis potential.

作者信息

Sun Ying, Zheng Xiaoyuan, Yuan Hui, Chen Geng, Ouyang Jiahe, Liu Jingfeng, Liu Xiaolong, Xing Xiaohua, Zhao Bixing

机构信息

The United Innovation of Mengchao Hepatobiliary Technology Key Laboratory of Fujian Province, Mengchao Hepatobiliary Hospital of Fujian Medical University, Fuzhou 350025, People's Republic of China; School of Life Sciences, Fujian Agriculture and Forestry University, Fuzhou 350002, People's Republic of China; Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002, People's Republic of China.

The United Innovation of Mengchao Hepatobiliary Technology Key Laboratory of Fujian Province, Mengchao Hepatobiliary Hospital of Fujian Medical University, Fuzhou 350025, People's Republic of China.

出版信息

J Proteomics. 2020 Aug 15;225:103834. doi: 10.1016/j.jprot.2020.103834. Epub 2020 May 23.

Abstract

Hepatocellular carcinoma (HCC) is one of the most common malignant tumours, metastasis and recurrence remain the primary reasons for poor prognosis. Ubiquitination serves as a degradation mechanism of proteins, but it is involved in additional cellular processes including metastasis. Here, by using label-free quantification, double-glycine (di-Gly) antibody affinity purification and high-resolution liquid chromatography tandem mass spectrometry (LC-MS/MS), we investigated quantitative proteome, ubiquitylome, and the crosstalk between the two datasets in HCC cell lines with different metastasis potential to identify biomarkers associated with HCC metastasis. In total, 83 ubiquitinated proteins significantly and steadily changed their abundance according to their metastatic potential, and the participated biological processes of these ubiquitinated proteins were tightly associated with tumour metastasis. Further signaling pathway analysis revealed that the ribosome and proteasome were significantly over-activated in the highly metastatic cells. Furthermore, we analyzed the crosstalk between the whole proteome and the ubiquitylome, and further discussed the mechanism that how ubiquitination events affect HCC metastasis. Eventually, the ubiquitination of Ku80 was validated to be significantly down-regulated in the high-metastatic cells comparing with the low-metastatic cells. We believe that these findings will help us better understand the underlying molecular mechanisms of the metastasis of HCC. SIGNIFICANCE: In this manuscript, we used label free based proteomics combined with diglycine antibody (di-Gly) affinity purification approach to identify biomarkers associated with HCC recurrence/metastasis in in a serial HCC cell lines with increasing invasion and metastasis potential. And then, we analyzed the crosstalk between the whole proteome and the ubiquitylome. Eventually, the ubiquitination of Ku80 was confirm to be closely associated with invasion and migration of HCC cells. As far as we know, this is the first time to use quantitative proteomic approach to study the ubiquitylomics in HCC cell lines with increasing metastasis ability.

摘要

肝细胞癌(HCC)是最常见的恶性肿瘤之一,转移和复发仍然是预后不良的主要原因。泛素化作为一种蛋白质降解机制,但它还参与包括转移在内的其他细胞过程。在这里,我们通过无标记定量、双甘氨酸(di-Gly)抗体亲和纯化和高分辨率液相色谱串联质谱(LC-MS/MS),研究了具有不同转移潜能的肝癌细胞系中的定量蛋白质组、泛素化蛋白质组以及这两个数据集之间的相互作用,以鉴定与肝癌转移相关的生物标志物。总共,83种泛素化蛋白根据其转移潜能显著且稳定地改变了丰度,这些泛素化蛋白参与的生物学过程与肿瘤转移密切相关。进一步的信号通路分析表明,核糖体和蛋白酶体在高转移细胞中显著过度激活。此外,我们分析了整个蛋白质组和泛素化蛋白质组之间的相互作用,并进一步讨论了泛素化事件如何影响肝癌转移的机制。最终,与低转移细胞相比,高转移细胞中Ku80的泛素化被证实显著下调。我们相信这些发现将有助于我们更好地理解肝癌转移的潜在分子机制。意义:在本论文中,我们使用基于无标记的蛋白质组学结合双甘氨酸抗体(di-Gly)亲和纯化方法,在一系列侵袭和转移潜能不断增加的肝癌细胞系中鉴定与肝癌复发/转移相关的生物标志物。然后,我们分析了整个蛋白质组和泛素化蛋白质组之间的相互作用。最终,证实Ku80的泛素化与肝癌细胞的侵袭和迁移密切相关。据我们所知,这是首次使用定量蛋白质组学方法研究转移能力不断增加的肝癌细胞系中的泛素化蛋白质组学。

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