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血管内皮生长因子及其受体在门静脉高压性胃病中的表达及其意义 被引量:2

Expression of vascular endothelial growth factor and its receptor in portal hypertensive gastropathy.
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摘要 目的 探讨血管内皮生长因子(VEGF)及其受体FLT-1、FLK-1mRNA在门静脉高压性胃病(PHG)中的作用。方法 采用逆转录聚合酶链反应(RT-PER)对44例肝硬化门静脉高压症患者PHG动态变化过程中病变部位的VEGF、FLT-1及FLK-1mRNA的表达进行检测。结果 轻度胃病组VEGF、FLT-1、FLK-1mRNA的表达量分别为(2.28±0.33)、(0.59±0.17)和(0.56±0.14),与无胃病组及正常对照组比较差异均有显著性(均P〈0.01);重度胃病组VEGF、FLT-1、FLK-1mRNA分别为(3.48±1.02)、(0.68±0.20)和(0.71±0.18),与轻度胃病组、无胃病组及正常对照组比较差异均有显著性(均P〈0.01)。结论 VEGF及其受体FLT-1、FLK-1过度表达是胃病胃黏膜损害的重要因素之一。 Objective To study the role of vascular endothelial growth factor ( VEGF ) and its receptor FLT-1,FLK-1 mRNA in the development of portal hypertensive gastropathy (PHG). Methods The expression of VEGF and its receptor FLT-1, FLK-1 mRNA in 44 patients with PHG were analyzed by reverse transcription-polymerase chain reaction (RT-PCR). Results VEGF and its receptor FLT-1, FLK-1 mRNA were all detected in the gastric mucosa, with higher level in the moderate PHG than the patients without PHG and the normal controls [ ( 2.28 ± 0.33 ), ( 0.59 ± 0. 17 ), ( 0.56 ± 0.14 ) P 〈 0.01 respectively]. The expression of VEGF and its receptor FLT-1, FLK-1 mRNA were higher in the severe PHG than the moderate PHG and the patients without PHG [ (3.48 ± 1.02 ) , (0.68 ± 0.20 ), (0.71 ± 0.18 ) P 〈 0.01 respectively ]. Conclusion The expression of VEGF and its receptor FLT-1 ,FLK-1 mRNA is up-regulated in the portal hypertensive gastric mucosa,which are one of the important factors in the development of PHG.
出处 《中国综合临床》 北大核心 2007年第3期226-227,共2页 Clinical Medicine of China
基金 山西省青年科研基金资助项目(20031065)
关键词 门静脉高压性胃病 血管内皮生长因子 逆转录聚合酶链反应 Portal hypertensive gastropathy Vascular endothelial growth factor Reverse transcriptase polymerase chain reaction
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参考文献5

  • 1商中华,刘浔阳,黄飞舟,聂晚频,朱晒红,任树平.门静脉高压症胃黏膜血管内皮生长因子变化的研究[J].中华普通外科杂志,2004,19(3):136-137. 被引量:2
  • 2商中华,刘浔阳,黄飞舟,聂晚频,朱晒红,任树平.血管内皮生长因子在门静脉高压症胃病中的变化[J].中华实验外科杂志,2004,21(2):247-247. 被引量:4
  • 3Iwao T,Toyonaga A ,Su mino M ,et al. Portal hypertensive gastropathy in patients with cirrhosis [ J ]. Gastroenterology, 1992,102 ( 6 ) :2060 -2065.
  • 4Shweiki D, Itin A, Softer D, et al. Vascular endothelial growth factor induced by hypoxia may mediate hypoxia-initiated angiogensis[J]. Nature,1992,359(6398) :843-845.
  • 5Neufeld G, Cohen T, Gengrinovttch S, et al. Vascular endothelial growth factor (VEGF) and its receptors[ J]. Faseb J,1999,13(1) :9 -22.

二级参考文献5

  • 1Jones MK,Itani RM,Wang HT,et al.Activation of VEGF and Ras genes in gastric mucosa during angiogenic response to ethanol injury[].American Journal of Physiology.1999
  • 2Ichikawa Y,Tarnawski A,James I,et al.Distorted microangioarchitecture and impaired angiogenesis in gastric mucosa of portal hypertensive rats[].Gastroenterology.1994
  • 3Neufeld G,Cohen T,Gengrinovitch S,et al.Vascular endothelial growth factor (VEGF) and its receptors[].The FASEB Journal.1999
  • 4Papazian A,Braillon A,Dupas JL,et al.Portal hypertensive gastric mucosa: an endoscopic study[].Gut.1986
  • 5Dvorak HF,Nagy JA,Feng D,et al.Vascular permeability factor/vascular endothelial growth factor and the significance of microvascular hyperpermeability in angiogenesis[].Current Topics in Microbiology and Immunology.1999

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