Department of Haematology, Guy's and St. Thomas' NHS Foundation Trust, London, United Kingdom.
Department of Medical and Molecular Genetics, King's College London, London, United Kingdom.
Blood Adv. 2021 Feb 23;5(4):1059-1068. doi: 10.1182/bloodadvances.2020003172.
Approximately 10% to 15% of patients with essential thrombocythemia (ET) lack the common driver mutations, so-called "triple-negative" (TN) disease. We undertook a systematic approach to investigate for somatic mutations and delineate gene expression signatures in 46 TN patients and compared the results to those with known driver mutations and healthy volunteers. Deep, error-corrected, next-generation sequencing of peripheral blood mononuclear cells using the HaloPlexHS platform and whole-exome sequencing was performed. Using this platform, 10 (22%) of 46 patients had detectable mutations (MPL, n = 6; JAK2V617F, n = 4) with 3 of 10 cases harboring germline MPL mutations. RNA-sequencing and DNA methylation analysis were also performed by using peripheral blood mononuclear cells. Pathway analysis comparing healthy volunteers and ET patients (regardless of mutational status) identified significant enrichment for genes in the tumor necrosis factor, NFκB, and MAPK pathways and upregulation of platelet proliferative drivers such as ITGA2B and ITGB3. Correlation with DNA methylation showed a consistent pattern of hypomethylation at upregulated gene promoters. Interrogation of these promoter regions highlighted enrichment of transcriptional regulators, which were significantly upregulated in patients with ET regardless of mutation status, including CEBPβ and NFκB. For "true" TN ET, patterns of gene expression and DNA methylation were similar to those in ET patients with known driver mutations. These observations suggest that the resultant ET phenotype may, at least in part and regardless of mutation type, be driven by transcriptional misregulation and may propagate downstream via the MAPK, tumor necrosis factor, and NFκB pathways with resultant JAK-STAT activation. These findings identify potential novel mechanisms of disease initiation that require further evaluation.
大约 10%至 15%的原发性血小板增多症 (ET) 患者缺乏常见的驱动突变,即所谓的“三阴性” (TN) 疾病。我们采用系统的方法对 46 例 TN 患者进行了体细胞突变研究,并描绘了基因表达特征,然后将结果与已知的驱动突变患者和健康志愿者进行了比较。采用 HaloPlexHS 平台和全外显子测序对外周血单核细胞进行深度、纠错的下一代测序。通过该平台,46 例患者中有 10 例 (22%) 可检测到突变 (MPL,n = 6;JAK2V617F,n = 4),其中 3 例携带胚系 MPL 突变。还使用外周血单核细胞进行了 RNA 测序和 DNA 甲基化分析。将健康志愿者与 ET 患者(无论突变状态如何)进行比较的通路分析发现,肿瘤坏死因子、NFκB 和 MAPK 通路中的基因显著富集,血小板增殖驱动基因如 ITGA2B 和 ITGB3 上调。与 DNA 甲基化的相关性表明,上调基因启动子的低甲基化存在一致的模式。对这些启动子区域的研究强调了转录调节剂的富集,无论突变状态如何,ET 患者的转录调节剂都显著上调,包括 CEBPβ 和 NFκB。对于“真正”的 TN ET,基因表达和 DNA 甲基化模式与具有已知驱动突变的 ET 患者相似。这些观察结果表明,ET 表型至少部分地、无论突变类型如何,都可能是由转录失调驱动的,并且可能通过 MAPK、肿瘤坏死因子和 NFκB 途径传播,从而导致 JAK-STAT 激活。这些发现确定了需要进一步评估的潜在疾病起始新机制。