Skov Vibe, Thomassen Mads, Kjaer Lasse, Larsen Morten Kranker, Knudsen Trine A, Ellervik Christina, Kruse Torben A, Hasselbalch Hans Carl
Department of Hematology, Zealand University Hospital, Roskilde, Denmark.
Department of Clinical Genetics, Odense University Hospital, Odense, Denmark.
Eur J Haematol. 2023 Nov;111(5):805-814. doi: 10.1111/ejh.14081. Epub 2023 Aug 28.
The Philadelphia-negative chronic myeloproliferative neoplasms (MPNs) are associated with a huge comorbidity burden, including an increased risk of cardiovascular diseases. Recently, chronic inflammation has been suggested to be the driving force for clonal evolution and disease progression in MPN but also potentially having an impact upon the development of accelerated (premature) atherosclerosis.
Since chronic inflammation, atherosclerosis, and atherothrombosis are prevalent in MPNs and we have previously shown oxidative stress genes to be markedly upregulated in MPNs, we hypothesized that genes linked to development of atherosclerosis might be highly deregulated as well.
Using whole blood gene expression profiling in patients with essential thrombocythemia (ET; n = 19), polycythemia vera (PV; n = 41), or primary myelofibrosis (PMF; n = 9), we herein for the first time report aberrant expression of several atherosclerosis genes.
Of 84 atherosclerosis genes, 45, 56, and 46 genes were deregulated in patients with ET, PV, or PMF, respectively. Furthermore, BCL2L1, MMP1, PDGFA, PTGS1, and THBS4 were progressively significantly upregulated and BCL2 progressively significantly downregulated from ET over PV to PMF (all FDR <0.05).
We have for the first time shown massive deregulation of atherosclerosis genes in MPNs, likely reflecting the inflammatory state in MPNs in association with in vivo activation of leukocytes, platelets, and endothelial cells being deeply involved in the atherosclerotic process.
费城染色体阴性的慢性骨髓增殖性肿瘤(MPN)与巨大的合并症负担相关,包括心血管疾病风险增加。最近,慢性炎症被认为是MPN克隆进化和疾病进展的驱动力,而且可能对加速(过早)动脉粥样硬化的发展产生影响。
由于慢性炎症、动脉粥样硬化和动脉粥样硬化血栓形成在MPN中普遍存在,且我们之前已表明氧化应激基因在MPN中显著上调,因此我们推测与动脉粥样硬化发展相关的基因可能也高度失调。
通过对原发性血小板增多症(ET;n = 19)、真性红细胞增多症(PV;n = 41)或原发性骨髓纤维化(PMF;n = 9)患者进行全血基因表达谱分析,我们首次报告了几种动脉粥样硬化基因的异常表达。
在84个动脉粥样硬化基因中,ET、PV或PMF患者分别有45、56和46个基因失调。此外,从ET到PV再到PMF,BCL2L1、MMP1、PDGFA、PTGS1和THBS4逐渐显著上调,而BCL2逐渐显著下调(所有FDR<0.05)。
我们首次表明MPN中动脉粥样硬化基因大量失调,这可能反映了MPN中的炎症状态,与白细胞、血小板和内皮细胞的体内激活有关,而这些细胞在动脉粥样硬化过程中起重要作用。