血管紧张素Ⅱ诱导VEGF mRNA在人肝癌细胞中的表达
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邢雪E-mail:xingxue1964@163.com

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Expression of VEGF mRNA induced by angiotensinⅡ in human hepatic cancer cell line
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    摘要:

    目的:研究血管紧张素Ⅱ(AngⅡ)对人肝癌HepG2细胞血管内皮生长因子(VEGF) mRNA表达的影响。
    方法:体外培养人肝癌HepG2细胞,采用不同浓度的AngⅡ进行处理,收集处理后不同时点的细胞,采用逆转录-聚合酶链反应(RT-PCR)半定量法,分别检测AngⅡ处理前后HepG2细胞VEGF mRNA的表达;同时利用MTT法检测AngⅡ对HepG2细胞增殖的影响。
    结果:AngⅡ能刺激HepG2细胞增殖,并增强VEGF mRNA的表达(P<0.05)。这种作用呈浓度-时间依赖效应,当AngⅡ浓度为10-7 mol/L,时间为60 h时,这种作用达到最高值,且此作用可被AngⅡ 1型受体(AT1R)拮抗剂所阻断。
    结论:AngⅡ可以通过AT1R诱导人肝癌细胞VEGF mRNA的表达,对肝癌的生长及转移可能起到一定的促进作用。

    Abstract:

    Objective: To investigate the effects of angiotensin Ⅱ (Ang Ⅱ) on the expression of vascular endothelial growth factor (VEGF) in human hepatic cancer cell line Hep G2.
     Methods: Cultured Hep G2 cells were treated by AngⅡ with various concentrations and were collected at different time points. Then total RNA was extracted. The expression of VEGF mRNA in cultured Hep G2 was determined by relative quantitative reverse transcription polymerase chain reaction(RT-PCR),and the proliferation was detected by methyl thiazolyl tetrazolium (MTT).
     Results: AngⅡ stimulated the proliferation of HepG2 cells, and enhanced the expression of VEGF mRNA (P<0.05), which was dose-and time-dependent. When the concentration of AngⅡ was 10-7 mol/L and the time was 60 h, the effect reached the maximum, and  which could be suppressed by Angiotensin II type 1 receptor (AT1R) antagonist.
     Conclusions: The expression of VEGF mRNA can be induced by AngⅡin human hepatic cancer cell line Hep G2 through AT1R, which may play a definite role in tumor growth and metastasis.

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张建|邢雪, 韩宏光|葛忠.血管紧张素Ⅱ诱导VEGF mRNA在人肝癌细胞中的表达[J].中国普通外科杂志,2010,19(2):159-163.
DOI:10.7659/j. issn.1005-6947.2010.02.014

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  • 收稿日期:2010-01-04
  • 最后修改日期:2010-01-26
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  • 在线发布日期: 2010-02-15