华西口腔医学杂志

• 基础研究 • 上一篇    下一篇

普萘洛尔治疗增殖期血管瘤患者血管内皮生长因子-A及表皮生长因子样结构域7的表达分析

凌彬1,2 陈曼丽3 刘洁1,2 尹小朋1,2 林兆全1,2 龚忠诚1,2   

  1. 1.新疆医科大学第一附属医院颌面肿瘤外科;2.新疆医科大学口腔医学院•新疆维吾尔自治区口腔医学研究所,乌鲁木齐 830054;3.新疆医科大学第五附属医院口腔科,乌鲁木齐 830000
  • 出版日期:2014-10-01 发布日期:2014-10-01
  • 通讯作者: 林兆全,主任医师,学士,E-mail:lzqxhj@163.com
  • 作者简介:凌彬,主治医师,硕士,E-mail:lingbin.cmfs@gmail.com
  • 基金资助:

    新疆维吾尔自治区自然科学基金面上资助项目(201321-1A080)

Expression of serum and urinary vascular endothelial growth factor-A and epidermal growth factor-like domain 7 in proliferating hemangioma treated with propranolol

Ling Bin1,2, Chen Manli3, Liu Jie1,2, Yin Xiaopeng1,2, Lin Zhaoquan1,2, Gong Zhongcheng1,2.
  

  1. 1. Oncology Department of Oral and Maxillofacial Surgery, The First Teaching Hospital of Xinjiang Medical University, Urumqi 830054, China; 2. Stomatology College of Xinjiang Medical University; Stomatology Research Institute of Xinjiang Uygur Autonomous Region, Urumqi 830054, China; 3. Dept. of Stomatology, The Fifth Teaching Hospital of Xinjiang Medical University, Urumqi 830000, China
  • Online:2014-10-01 Published:2014-10-01

摘要:

目的 对普萘洛尔治疗增殖期婴幼儿血管瘤的临床疗效和治疗过程中血清及尿液血管内皮生长因子-A(VEGF-A)和表皮生长因子样结构域7(EGFL7)表达水平进行检测分析。方法 选择30例婴幼儿增殖期血管瘤患者为研究对象,口服普萘洛尔治疗4~8个月,口服剂量为每天0.5~2 mg•kg-1。采用B超测量治疗前后瘤体的半径,采用Achauer疗效评定法进行临床疗效评估。采用酶联免疫吸附法(ELISA)检测治疗前、治疗后4周、治疗后12周血清及尿液中VEGF-A和EGFL7水平。结果 治疗效果评价:2例优,11例好,14例中等,3例差。治疗前血清VEGF-A水平最高(335.692 pg•mL-1±136.146 pg•mL-1),治疗后4周(264.853 pg•mL-1±122.120 pg•mL-1)和治疗后12周(211.345 pg•mL-1±104.035 pg•mL-1)呈逐渐下降趋势,治疗后4、12周血清VEGF-A水平低于治疗前(P<0.05)。治疗前尿液VEGF-A水平最高(76.234 pg•mL-1±24.169 pg•mL-1),治疗后4周(56.454 pg•mL-1±16.111 pg•mL-1)和治疗后12周(34.728 pg•mL-1±12.656 pg•mL-1)呈逐渐下降趋势,治疗后4、12周尿液VEGF-A水平低于治疗前(P< 0.05)。血清和尿液中EGFL7的表达趋势与VEGF-A一致。结论 普萘洛尔能够安全有效地治疗增殖期婴幼儿血管瘤。普萘洛尔能降低增殖期婴幼儿血管瘤患者外周血清和尿液中VEGF-A和EGFL7水平。

关键词: 普萘洛尔, 增殖期婴幼儿血管瘤, 血管内皮生长因子-A, 表皮生长因子样结构域7

Abstract:

Objective This study aims to investigate the expression levels of serum and urinary vascular endothelial growth factor-A (VEGF-A) and epidermal growth factor-like domain 7 (EGFL7) in proliferating infantile hemangioma patients under propranolol treatment. Methods Propranolol (0.5–2 mg•kg−1) was orally administered to 30 infants every day for 4–8 months. The Achauer method was used to measure the tumor radius and thus evaluate the clinical curative effects of the treatment. Enzyme-linked immunosorbent assay was used to measure the serum and urinary concentrations of VEGF-A and EGFL7 at 0, 4, and 12 weeks after the treatment. Results The treatment response was excellent in 2 patients, good in 11, moderate in 14, and poor in 3. Serum VEGF-A (335.692 pg•mL−1±136.146 pg•mL−1) was high before the treatment and then significantly decreased after 4 weeks (264.853 pg•mL−1±122.120 pg•mL−1) and 12 weeks (211.345 pg•mL−1±104.035 pg•mL−1) of treatment (P<0.05). Urinary VEGF-A (76.234 pg•mL−1±24.169 pg•mL−1) was high before the treatment and then significantly decreased after four weeks (56.454 pg•mL−1±16.111 pg•mL−1) and twelve weeks (34.728 pg•mL−1±12.656 pg•mL−1) of treatment (P<0.05). Serum and urinary EGFL7 also decreased after the treatment, showing a positive relationship with VEGF-A. Conclusion Propranolol can be safely and effectively used to treat proliferating infantile hemangiomas. This treatment can reduce the peripheral serum and urinary concentrations of VEGF-A and EGFL7 in affected children.

Key words: propranolol, proliferating infantile haemangioma, vascular endothelial growth factor-A, epidermal growth factor-like domain 7