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Role of Microvessel Density and Vascular Endothelial Growth Factor in Angiogenesis of Hematological Malignancies.微血管密度和血管内皮生长因子在血液系统恶性肿瘤血管生成中的作用
Bone Marrow Res. 2016;2016:5043483. doi: 10.1155/2016/5043483. Epub 2016 Feb 22.
2
Role of tumour angiogenesis in haematological malignancies.肿瘤血管生成在血液系统恶性肿瘤中的作用。
Swiss Med Wkly. 2014 Nov 6;144:w14050. doi: 10.4414/smw.2014.14050. eCollection 2014.
3
Serum cytokine and adhesion molecule profile differs in newly diagnosed acute myeloid and lymphoblastic leukemia.新诊断的急性髓系白血病和急性淋巴细胞白血病患者的血清细胞因子和黏附分子谱有所不同。
Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2015 Jun;159(2):299-301. doi: 10.5507/bp.2014.051. Epub 2014 Oct 29.
4
Serum vascular endothelial growth factor-a levels during induction therapy in children with acute lymphoblastic leukemia.血清血管内皮生长因子-a 在儿童急性淋巴细胞白血病诱导治疗期间的水平。
Indian Pediatr. 2013 Jul;50(7):659-62. doi: 10.1007/s13312-013-0198-6. Epub 2012 Dec 5.
5
Vascular endothelial growth factor levels in childhood acute lymphoblastic and myeloblastic leukemia.儿童急性淋巴细胞白血病和急性髓细胞白血病中的血管内皮生长因子水平
Indian J Hematol Blood Transfus. 2012 Mar;28(1):24-8. doi: 10.1007/s12288-011-0102-2. Epub 2011 Aug 17.
6
Plasma cytokine profiles at diagnosis in pediatric patients with non-hodgkin lymphoma.非霍奇金淋巴瘤儿科患者诊断时的血浆细胞因子谱
J Pediatr Hematol Oncol. 2012 May;34(4):271-5. doi: 10.1097/MPH.0b013e3182431e02.
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Leukemia stem cells and microenvironment: biology and therapeutic targeting.白血病干细胞与微环境:生物学与治疗靶点
J Clin Oncol. 2011 Feb 10;29(5):591-9. doi: 10.1200/JCO.2010.31.0904. Epub 2011 Jan 10.
8
Angiogenesis factor pattern differs in acute lymphoblastic leukemia and chronic lymphocytic leukemia.血管生成因子模式在急性淋巴细胞白血病和慢性淋巴细胞白血病中有所不同。
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9
Correlation between high vascular endothelial growth factor-A serum levels and treatment outcome in patients with standard-risk acute lymphoblastic leukemia: a report from Children's Oncology Group Study CCG-1962.高危急性淋巴细胞白血病患者血清高血管内皮生长因子-A水平与治疗结果的相关性:儿童肿瘤学组CCG-1962研究报告
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基于血清血管内皮生长因子检测评估急性淋巴细胞白血病患儿的血管生成情况。

Assessment of Angiogenesis in Children with Acute Lymphoblastic Leukemia Based on Serum Vascular Endothelial Growth Factor Assay.

作者信息

Mizia-Malarz Agnieszka, Sobol-Milejska Grazyna

机构信息

Department of Paediatric Oncology, Haematology and Chemotherapy, Upper Silesian Children's Healthcare Centre, Medical University of Silesia, Katowice, Poland.

出版信息

Indian J Med Paediatr Oncol. 2017 Jul-Sep;38(3):321-325. doi: 10.4103/ijmpo.ijmpo_109_17.

DOI:10.4103/ijmpo.ijmpo_109_17
PMID:29200682
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5686975/
Abstract

INTRODUCTION

Vascular endothelial growth factor A (VEGFA) is a key proangiogenic cytokine. The role of angiogenesis in acute lymphoblastic leukemia (ALL) is still unclear. The purpose of the study was to assess angiogenesis in children with ALL based on serum VEGFA level determined at diagnosis and at remission with further participant subdivision into different risk groups.

MATERIALS AND METHODS

Forty children, aged 3-12 years (mean age: 8 years) with newly diagnosed ALL, were enrolled in the study. The control group (Group C) was twenty healthy children. According to the risk assessment, they were classified into a standard-risk group, an intermediate-risk group (IRG), or a high-risk group (HRG).

RESULTS

The median serum VEGFA levels at diagnosis were significantly higher in IRG and HRG as compared to Group C. The VEGFA levels at remission were significantly higher in all study groups, as compared to Group C. The differences in median values of serum VEGFA levels between the study groups both at diagnosis and at remission were not statistically significant.

CONCLUSIONS

The angiogenesis in ALL seems to be intensified at diagnosis as a result of neoplasmatic bone marrow rebuilding and at remission as its intensive recovering.

摘要

引言

血管内皮生长因子A(VEGFA)是一种关键的促血管生成细胞因子。血管生成在急性淋巴细胞白血病(ALL)中的作用仍不明确。本研究的目的是基于诊断时和缓解时测定的血清VEGFA水平评估ALL患儿的血管生成情况,并将参与者进一步细分为不同风险组。

材料与方法

40名年龄在3至12岁(平均年龄:8岁)的新诊断ALL患儿纳入本研究。对照组(C组)为20名健康儿童。根据风险评估,他们被分为标准风险组、中危组(IRG)或高危组(HRG)。

结果

与C组相比,IRG和HRG在诊断时的血清VEGFA水平中位数显著更高。与C组相比,所有研究组在缓解时的VEGFA水平均显著更高。研究组在诊断时和缓解时血清VEGFA水平中位数的差异均无统计学意义。

结论

ALL中的血管生成在诊断时似乎因肿瘤性骨髓重建而增强,在缓解时因骨髓的强烈恢复而增强。