Atesoglu Elif Birtas, Tarkun Pinar, Mehtap Ozgur, Demirsoy Esra Terzi, Atalay Figen, Maden Muhammet, Celebi Koray, Hacihanefioglu Abdullah
Department of Hematology, Kocaeli University Hospital, Umuttepe, 41380 Kocaeli, Turkey.
Department of Hematology, Baskent University, Istanbul, Turkey.
Indian J Hematol Blood Transfus. 2016 Jun;32(2):162-7. doi: 10.1007/s12288-015-0548-8. Epub 2015 May 16.
Molecular balance between Angiopoietin-1 (Ang-1) and Angiopoietin-2 (Ang-2) has important effects in tumor angiogenesis. Ang-2 was shown to be elevated and proved to be a prognostic factor in acute myeloid leukemia (AML). To date studies revealed increased angiogenesis in bone marrows (BMs) of both myeloproliferative neoplasm (MPN) and AML patients. We conducted this study to demonstrate circulating levels of Ang-1 and Ang-2 in MPN patients since no data exists in literature. Thirty-three newly diagnosed MPN, 27 newly diagnosed AML patients and 25 controls (HC) were enrolled and Angiopoietin levels were determined with ELISA. We found that Ang-1 levels were higher whereas Ang-2 levels were lower in MPN and HC when compared to AML. Our results suggest that though angiogenesis is increased in both AML and MPN, angiopoietin serum level profile of the two diseases are different, and MPN patients have similar Ang-1 and Ang-2 levels as HC. We conclude that, according to our results Ang-1 and Ang-2 do not only regulate tumor angiogenesis and the difference between angiopoietin levels of acute and chronic myeloid neoplasms could be a reflection of other effects of these growth factors on tumor malignancy.
血管生成素-1(Ang-1)与血管生成素-2(Ang-2)之间的分子平衡在肿瘤血管生成中具有重要作用。研究表明,急性髓系白血病(AML)患者体内Ang-2水平升高,且被证实为预后因素。迄今为止的研究显示,骨髓增殖性肿瘤(MPN)患者和AML患者的骨髓(BM)血管生成均增加。由于文献中尚无相关数据,我们开展了本研究以测定MPN患者的循环Ang-1和Ang-2水平。招募了33例新诊断的MPN患者、27例新诊断的AML患者和25例对照(HC),采用酶联免疫吸附测定法(ELISA)测定血管生成素水平。我们发现,与AML患者相比,MPN患者和HC的Ang-1水平较高,而Ang-2水平较低。我们的结果表明,虽然AML和MPN患者的血管生成均增加,但这两种疾病的血管生成素血清水平谱不同,且MPN患者的Ang-1和Ang-2水平与HC相似。我们得出结论,根据我们的结果,Ang-1和Ang-2不仅调节肿瘤血管生成,急性和慢性髓系肿瘤血管生成素水平的差异可能反映了这些生长因子对肿瘤恶性程度的其他影响。