Anagnostopoulos Athanasios, Eleftherakis-Papaiakovou Vangelis, Kastritis Efstathios, Tsionos Konstantinos, Bamias Aristotelis, Meletis John, Dimopoulos Meletios A, Terpos Evangelos
Department of Clinical Therapeutics, University of Athens School of Medicine, Alexandra General Hospital, Athens, Greece.
Br J Haematol. 2007 Jun;137(6):560-8. doi: 10.1111/j.1365-2141.2007.06609.x.
Angiogenesis represents an essential step of disease progression in several haematological malignancies. Microvessel density is increased in 30% of patients with Waldenstrom macroglobulinaemia (WM), but there is very limited information regarding the role of angiogenic cytokines in this disease. Serum levels of vascular endothelial growth factor (VEGF), VEGF-A, angiogenin, angiopoietin (Ang)-1 and -2, and basic fibroblast growth factor (bFGF) were evaluated in 56 WM patients at different disease phases (24 untreated, 20 relapsed/refractory and 12 patients at remission) and 11 patients with immunoglobulin M type monoclonal gammopathy of undetermined significance (IgM-MGUS). All patients had increased levels of angiogenin, VEGF, VEGF-A, and bFGF compared with controls. The Ang-1/Ang-2 ratio was reduced in WM but not in IgM-MGUS patients. Angiogenin levels correlated with disease status: when compared with healthy subjects, patients with IgM-MGUS and untreated WM patients had increased angiogenin serum levels, which were higher in untreated WM patients than in MGUS. WM patients at remission had lower angiogenin serum levels compared with untreated patients, but these levels were increased again in active disease post-therapy. Angiogenin also correlated with albumin levels, while VEGF-A correlated with beta(2)-microglobulin (beta2M). Ang-1/Ang-2 ratio showed a strong, negative correlation with beta2M, and positive correlation with albumin, haemoglobin and lymphadenopathy. Our results indicate a potential use of angiogenin levels for follow-up in WM and angiogenic molecules as targets for the development of novel anti-WM agents.
血管生成是几种血液系统恶性肿瘤疾病进展的关键步骤。30%的华氏巨球蛋白血症(WM)患者微血管密度增加,但关于血管生成细胞因子在该疾病中的作用的信息非常有限。对56例处于不同疾病阶段的WM患者(24例未治疗、20例复发/难治性和12例缓解期患者)以及11例意义未明的免疫球蛋白M型单克隆丙种球蛋白病(IgM-MGUS)患者的血清血管内皮生长因子(VEGF)、VEGF-A、血管生成素、血管生成素(Ang)-1和-2以及碱性成纤维细胞生长因子(bFGF)水平进行了评估。与对照组相比,所有患者的血管生成素、VEGF、VEGF-A和bFGF水平均升高。WM患者的Ang-1/Ang-2比值降低,但IgM-MGUS患者未降低。血管生成素水平与疾病状态相关:与健康受试者相比,IgM-MGUS患者和未治疗的WM患者血清血管生成素水平升高,未治疗的WM患者高于MGUS患者。缓解期的WM患者血清血管生成素水平低于未治疗患者,但在治疗后疾病活动期这些水平再次升高。血管生成素还与白蛋白水平相关,而VEGF-A与β2-微球蛋白(β2M)相关。Ang-1/Ang-2比值与β2M呈强烈负相关,与白蛋白、血红蛋白和淋巴结病呈正相关。我们的结果表明血管生成素水平在WM随访中的潜在用途以及血管生成分子作为新型抗WM药物开发靶点的可能性。