Hou Hsin-An, Chou Wen-Chien, Lin Liang-In, Tang Jih-Luh, Tseng Mei-Hsuan, Huang Chi-Fei, Yao Ming, Chen Chien-Yuan, Tsay Woei, Tien Hwei-Fang
Division of Hematology, Department of Internal Medicine, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, Taiwan.
Leuk Res. 2008 Jun;32(6):904-12. doi: 10.1016/j.leukres.2007.08.010. Epub 2007 Sep 29.
Angiogenic factors play an essential role in normal and pathologic angiogenesis, but their clinical role in acute myeloid leukemia (AML) remains unclear. We investigated the expression of Ang-1, Ang-2, Tie2, VEGF-A, and VEGF-C genes in bone marrow (BM) mononuclear cells by real-time quantitative PCR (RQ-PCR) in a cohort of 126 patients with newly diagnosed de novo AML and normal marrow donors. Here we show that high pre-treatment levels of Ang-2 in the BM indicate an unfavorable prognosis in AML. Only karyotype (hazard ratio 2.19, 95% CI 1.25-3.42, P=0.005) and expression of Ang-2 (hazard ratio 2.05, 95% CI 1.20-3.52, P=0.009), but not other angiogenic factors, were independent prognostic factors for overall survival by multivariate analysis. The prognostic significance of Ang-2 expression was more obvious in the subgroup of patients with intermediate-risk cytogenetics. Subgroup analysis showed that Ang-2 expression had prognostic impact on patients with low (but not high) Ang-1 or Tie2 levels, and on patients with high (but not low) VEGF-A or VEGF-C levels.
血管生成因子在正常和病理性血管生成中发挥着重要作用,但其在急性髓系白血病(AML)中的临床作用仍不清楚。我们通过实时定量PCR(RQ-PCR)检测了126例新诊断的初发AML患者及正常骨髓供者队列中骨髓(BM)单个核细胞中Ang-1、Ang-2、Tie2、VEGF-A和VEGF-C基因的表达。我们发现,BM中Ang-2的预处理水平较高表明AML预后不良。多因素分析显示,只有核型(风险比2.19,95%可信区间1.25 - 3.42,P = 0.005)和Ang-2的表达(风险比2.05,95%可信区间1.20 - 3.52,P = 0.009),而非其他血管生成因子,是总生存的独立预后因素。Ang-2表达的预后意义在中危细胞遗传学亚组患者中更为明显。亚组分析显示,Ang-2表达对低(而非高)Ang-1或Tie2水平的患者以及高(而非低)VEGF-A或VEGF-C水平的患者具有预后影响。