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Expression of vascular endothelial growth factor receptor 3 and Tie1 tyrosine kinase receptor on acute leukemia cells.

机译:血管内皮生长因子受体3和Tie1酪氨酸激酶受体在急性白血病细胞中的表达

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BACKGROUND: Recent data indicate a role for angiogenesis in hematologic malignancies. In addition to promoting new vessel growth in the bone marrow microenvironment, angiogenic factors are regulators of both hematopoietic and leukemic cells. Activation of vascular endothelial growth factor receptor 3 (VEGFR-3) and Tie1 tyrosine kinase receptor are known to promote leukemia cell survival. The details of this complex angiogenesis-related interaction are still uncertain. PROCEDURE: We studied bone marrow samples from 73 patients with acute lymphoblastic (ALL) or myelogenous (AML) leukemia by using immunological methods. RESULTS: Vascular endothelial growth factor receptor 3 expression was found in 15% of the samples, particularly in samples with pediatric lymphoblastic leukemias and monocytic AMLs. Tie1 protein expression was found in 11% of the samples, all of which were from adult AML patients. CONCLUSIONS: Our findings suggest that there are angiogenesis-related differences between pediatric and adult lymphoblastic leukemias as well as between lymphoid and myeloid leukemias.
机译:背景:最近的数据表明血管生成在血液系统恶性肿瘤中的作用。除了促进骨髓微环境中新血管的生长外,血管生成因子还是造血细胞和白血病细胞的调节剂。已知血管内皮生长因子受体3(VEGFR-3)和Tie1酪氨酸激酶受体的激活可促进白血病细胞的存活。这种复杂的血管生成相关相互作用的细节仍不确定。程序:我们使用免疫学方法研究了73例急性淋巴细胞白血病(ALL)或骨髓性(AML)白血病患者的骨髓样本。结果:在15%的样本中发现了血管内皮生长因子受体3的表达,特别是在患有小儿淋巴细胞白血病和单核AML的样本中。在11%的样本中发现了Tie1蛋白表达,所有样本均来自成年AML患者。结论:我们的发现表明,小儿和成人淋巴细胞白血病以及淋巴样和髓样白血病之间存在血管生成相关的差异。

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