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达沙替尼抑制真性红细胞增多症祖细胞的增殖。

Dasatinib inhibits progenitor cell proliferation from polycythaemia vera.

作者信息

Wappl M, Jaeger E, Streubel B, Gisslinger H, Schwarzinger I, Valent P, Oehler L

机构信息

Medical University of Vienna, Austria.

出版信息

Eur J Clin Invest. 2008 Aug;38(8):578-84. doi: 10.1111/j.1365-2362.2008.01982.x.

Abstract

BACKGROUND

A mutation of Janus kinase 2 V617F is present in most patients with polycythaemia vera (PV). However, it is generally believed that JAK2(V617F) is not the sole molecular abnormality in PV. Since dasatinib is currently evaluated in patients with PV, it is of interest to study the effects of dasatinib on the growth of clonal progenitor cells in vitro.

DESIGN AND METHODS

Peripheral blood mononuclear cells from patients with PV, chronic myeloid leukaemia (CML) and controls were exposed to dasatinib (0.1 to 500 nm mL(-1)). Colony growth was stimulated by interleukin-3, granulocyte-macrophage colony-stimulating factor and erythropoietin. Endogenous erythroid colony (EEC) growth was investigated without exogenous cytokines. Real-time PCR was performed to assess the percentage of JAK2(V617F) cells.

RESULTS

10 nm of dasatinib suppressed EEC growth from PV by 89% (P = 0.002). This inhibition was dose dependent and occurred at pharmacological concentrations. Erythroid and myeloid colony growth was also significantly suppressed in the presence of exogenous cytokines. When compared to PV the inhibition of stimulated colony growth was significantly less pronounced in controls but tended to be more vigorous in CML. Interestingly, despite the potent inhibition of PV cells real-time PCR revealed that the numbers of JAK2(V617F) transcripts did not decrease upon exposure to dasatinib.

CONCLUSION

This study shows a marked inhibition of the proliferative capacity of progenitor cells from PV. Although JAK2(V617F) transcript levels did not decrease upon exposure to dasatinib, the drug might suppress PV progenitors through inhibition of a yet undefined molecular target.

摘要

背景

大多数真性红细胞增多症(PV)患者存在Janus激酶2 V617F突变。然而,人们普遍认为JAK2(V617F)并非PV唯一的分子异常。由于目前正在对PV患者进行达沙替尼评估,因此研究达沙替尼对体外克隆祖细胞生长的影响具有重要意义。

设计与方法

将PV患者、慢性髓性白血病(CML)患者及对照者的外周血单个核细胞暴露于达沙替尼(0.1至500 nM mL⁻¹)。通过白细胞介素-3、粒细胞-巨噬细胞集落刺激因子和促红细胞生成素刺激集落生长。在无外源性细胞因子的情况下研究内源性红系集落(EEC)生长。进行实时聚合酶链反应以评估JAK2(V617F)细胞的百分比。

结果

10 nM的达沙替尼可使PV患者的EEC生长抑制89%(P = 0.002)。这种抑制呈剂量依赖性,且发生在药理浓度下。在外源性细胞因子存在的情况下,红系和髓系集落生长也受到显著抑制。与PV相比,对照者中刺激集落生长的抑制作用明显较弱,但在CML中则更明显。有趣的是,尽管达沙替尼对PV细胞有强大的抑制作用,但实时聚合酶链反应显示,暴露于达沙替尼后JAK2(V617F)转录本数量并未减少。

结论

本研究表明PV祖细胞的增殖能力受到显著抑制。尽管暴露于达沙替尼后JAK2(V617F)转录水平未降低,但该药物可能通过抑制尚未明确的分子靶点来抑制PV祖细胞。

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