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High expression of KITLG is a new hallmark activating the MAPK pathway in type A and AB thymoma

机译:Kitlg的高表达是一种激活A和AB胸腺瘤的MAPK途径的新标志

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BACKGROUND:KIT proto-oncogene ligand (KITLG) is a pleiotropic factor which is found in diverse cancers and is involved in cell proliferation, differentiation, and survival. However, the value of KITLG in thymoma remains unclear.METHODS:A total of 121 thymoma samples from The Cancer Genome Atlas Thymoma (TCGA-THYM) dataset were used to analyze KITLG related genome-wide expression profiles, and microRNA profiles and methylation alterations and a GEO dataset-GSE29695, including 37 samples was used as verification. For cell-based studies, specific small interfering RNA targeting KITLG or a KITLG overexpression vector were used to clarify the changes of the MAPK pathway in an AB thymoma cell line Thy0517.RESULTS:Both datasets showed that high expression of KITLG was significantly associated with type A and AB thymoma. Through multiomic analysis of the TCGA-THYM, it was found that with the high expression of KITLG, there were 220 upregulated and 72 downregulated genes at the mRNA level, 79 positive and 78 negative miRNAs, 28 hypermethylation and 163 hypomethylation regions. In the thymoma cell line Thy0517, it was found that the expression of GRB2 and the phosphorylation levels of BRAF, MEK1/2, and ERK1/2 in the MAPK pathway were positively correlated with the change in KITLG.CONCLUSIONS:High expression of KITLG is a new hallmark of WHO type A and AB thymomas in which it might play a critical role through the activation of the MAPK signaling pathway. Additionally, it is hoped that KITLG will become a potential target for the diagnosis of type A and AB thymoma through further research in the future.KEY POINTS:SIGNIFICANT FINDINGS OF THE STUDY: KIT proto-oncogene ligand (KITLG) is a new hallmark of type A and AB thymomas which induce a series of aberrant alteration of mRNA, miRNA and DNA methylation. The expression of KITLG is significantly higher in type A and AB than other subtypes of thymoma.WHAT THIS STUDY ADDS:KITLG activated the MAPK signaling pathway to promote type A and AB thymoma which might be a potential diagnostic biomarker or target.? 2020 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd.
机译:背景:套件原癌基因配体(KITLG)是一种在不同癌症中发现的抗脂肪因子,并且参与细胞增殖,分化和存活。然而,Kitlg在胸腺瘤中的价值仍然尚不清楚。方法:使用来自癌症基因组胸腺瘤(TCGA-Thym)数据集的总共121个胸腺瘤样品分析Kitlg相关的基因组的表达谱,以及微瘤谱和甲基化改变和甲基化改变使用GEO数据集-GSE29695,包括37个样本作为验证。对于基于细胞的研究,使用特异性小干扰RNA靶向KITLG或KITLG过表达载体,阐明AB胸腺瘤细胞系中MAPK途径的变化。结果:两种数据集表明KITLG的高表达与类型显着相关A和AB胸腺瘤。通过对TCGA-THYM的多元分析,发现随着KITLG的高表达,MRNA水平的220个上调和72个下调基因,79阳性和78个阴性miRNA,28个高甲基化和163个低甲基化区域。在胸腺瘤细胞系THY0517中,发现GRB2的表达和BRAF,MEK1 / 2和ERK1 / 2在MAPK途径中的表达与Kitlg.Conclusions的变化呈正相关:Kitlg的高表达是谁键入A和AB胸腺瘤的新标志,其中通过激活MAPK信令路径可能发挥关键作用。此外,希望Kitlg将通过未来进一步研究成为A和AB胸腺瘤诊断的潜在目标.KEY点:研究的重要发现:Kit原癌基因配体(Kitlg)是一个新的标志型A和AB胸膜瘤瘤,其诱导mRNA,miRNA和DNA甲基化的一系列异常改变。 A型和AB的表达明显高于胸腺瘤的其他亚型。本研究补充说:Kitlg激活MAPK信号通路以促进A和AB胸腺瘤,其可能是潜在的诊断生物标志物或靶标。 2020作者。中国肺部肿瘤集团和约翰瓦里和儿子澳大利亚发表的胸癌

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