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通过蛋白质组学分析鉴定间变性甲状腺癌细胞中的BAG3靶蛋白。

Identification of BAG3 target proteins in anaplastic thyroid cancer cells by proteomic analysis.

作者信息

Galdiero Francesca, Bello Anna Maria, Spina Anna, Capiluongo Anna, Liuu Sophie, De Marco Margot, Rosati Alessandra, Capunzo Mario, Napolitano Maria, Vuttariello Emilia, Monaco Mario, Califano Daniela, Turco Maria Caterina, Chiappetta Gennaro, Vinh Joëlle, Chiappetta Giovanni

机构信息

Functional Genomic Unit, Istituto Nazionale Tumori-IRCCS-Fondazione G. Pascale, Napoli, Italia.

ESPCI ParisTech, Spectrométrie de Masse Biologique et Protéomique (SMBP), USR3149 CNRS, Paris, France.

出版信息

Oncotarget. 2018 Jan 3;9(8):8016-8026. doi: 10.18632/oncotarget.23858. eCollection 2018 Jan 30.

Abstract

BAG3 protein is an apoptosis inhibitor and is highly expressed in Anaplastic Thyroid Cancer. We investigated the entire set of proteins modulated by BAG3 silencing in the human anaplastic thyroid 8505C cancer cells by using the Stable-Isotope Labeling by Amino acids in Cell culture strategy combined with mass spectrometry analysis. By this approach we identified 37 up-regulated and 54 down-regulated proteins in BAG3-silenced cells. Many of these proteins are reportedly involved in tumor progression, invasiveness and resistance to therapies. We focused our attention on an oncogenic protein, CAV1, and a tumor suppressor protein, SERPINB2, that had not previously been reported to be modulated by BAG3. Their expression levels in BAG3-silenced cells were confirmed by qRT-PCR and western blot analyses, disclosing two novel targets of BAG3 pro-tumor activity. We also examined the dataset of proteins obtained by the quantitative proteomics analysis using two tools, Downstream Effect Analysis and Upstream Regulator Analysis of the Ingenuity Pathways Analysis software. Our analyses confirm the association of the proteome profile observed in BAG3-silenced cells with an increase in cell survival and a decrease in cell proliferation and invasion, and highlight the possible involvement of four tumor suppressor miRNAs and TP53/63 proteins in BAG3 activity.

摘要

BAG3蛋白是一种凋亡抑制剂,在间变性甲状腺癌中高表达。我们采用细胞培养中氨基酸稳定同位素标记策略结合质谱分析,研究了BAG3沉默在人8505C间变性甲状腺癌细胞中调节的全套蛋白质。通过这种方法,我们在BAG3沉默的细胞中鉴定出37种上调蛋白和54种下调蛋白。据报道,其中许多蛋白质与肿瘤进展、侵袭性和对治疗的抗性有关。我们将注意力集中在一种致癌蛋白CAV1和一种肿瘤抑制蛋白SERPINB2上,此前尚未报道它们受BAG3调节。通过qRT-PCR和蛋白质印迹分析证实了它们在BAG3沉默细胞中的表达水平,揭示了BAG3促肿瘤活性的两个新靶点。我们还使用两种工具,即通路分析软件的下游效应分析和上游调节因子分析,检查了通过定量蛋白质组学分析获得的蛋白质数据集。我们的分析证实了在BAG3沉默细胞中观察到的蛋白质组谱与细胞存活率增加、细胞增殖和侵袭减少之间的关联,并突出了四种肿瘤抑制性微小RNA和TP53/63蛋白在BAG3活性中的可能作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dab7/5814278/739b6db4458b/oncotarget-09-8016-g001.jpg

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