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特发性血小板增多症患者血浆血管生成因子和循环内皮细胞水平:与细胞减少治疗和 JAK2-V617F 突变状态的相关性。

Plasma levels of angiogenic factors and circulating endothelial cells in essential thrombocythemia: correlation with cytoreductive therapy and JAK2-V617F mutational status.

机构信息

Department of Hematology, Medical University of Łódź, Copernicus Memorial Hospital, Łódź, Poland.

出版信息

Leuk Lymphoma. 2010 Sep;51(9):1727-33. doi: 10.3109/10428194.2010.500435.

DOI:10.3109/10428194.2010.500435
PMID:20615083
Abstract

Recent studies have shown that angiogenesis plays an important role in the biology of hematological malignancies including essential thrombocythemia (ET). Using cytofluorimetric analysis, the levels of angiogenic factors, as well as the number of circulating endothelial cells (CECs), were determined in 65 patients with ET, including 33 previously untreated and 32 receiving cytoreductive therapy. Correlations between markers of angiogenesis and JAK2-V617F mutational status were also assessed. We found significantly higher levels of vascular endothelial growth factor (VEGF) and markedly decreased levels of placental growth factor in untreated patients with ET with respect to control subjects. VEGF levels were significantly increased in patients with white blood count >8.7 (x 10(9)/L) vs. <8.7 (x 10(9)/L). Furthermore, the levels of VEGF in patients on hydroxyurea (HU) therapy were markedly lower than in untreated patients. It was also demonstrated that the number of all CEC subpopulations (resting, activated, apoptotic, and circulating precursor endothelial cells) was increased in patients with ET in relation to controls, regardless of the JAK2-V617F status, and was not affected by cytoreductive treatment. In conclusion, our study highlights the possible role of angiogenesis in the pathophysiology of ET. It provides evidence that the number of CECs is elevated independently of JAK2-V617F status and is not down-regulated by HU or anagrelide therapy. Our data suggest that VEGF levels are particularly elevated in patients with high leukocytosis. Further investigation should be undertaken to determine the possible role of antiangiogenic therapy in ET.

摘要

最近的研究表明,血管生成在包括原发性血小板增多症(ET)在内的血液恶性肿瘤的生物学中起着重要作用。使用流式细胞分析,在 65 例 ET 患者中确定了血管生成因子的水平,以及循环内皮细胞(CEC)的数量,包括 33 例未经治疗和 32 例接受细胞减少治疗的患者。还评估了血管生成标志物与 JAK2-V617F 突变状态之间的相关性。我们发现未经治疗的 ET 患者的血管内皮生长因子(VEGF)水平明显升高,胎盘生长因子水平明显降低,与对照组相比。白细胞计数>8.7(x 10(9)/L)的患者 VEGF 水平明显高于白细胞计数<8.7(x 10(9)/L)的患者。此外,羟基脲(HU)治疗患者的 VEGF 水平明显低于未治疗患者。还表明,无论 JAK2-V617F 状态如何,ET 患者的所有 CEC 亚群(静止、激活、凋亡和循环前体细胞)的数量均高于对照组,并且不受细胞减少治疗的影响。总之,我们的研究强调了血管生成在 ET 病理生理学中的可能作用。它提供的证据表明,CEC 的数量升高与 JAK2-V617F 状态无关,并且不受 HU 或安格雷利德治疗的下调。我们的数据表明,白细胞增多症患者的 VEGF 水平特别升高。应进一步进行调查,以确定抗血管生成治疗在 ET 中的可能作用。

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