Tanshinone IIA inhibits gastric carcinoma AGS cells by decreasing the protein expression of VEGFR and blocking Ras/Raf/MEK/ERK pathway

被引:37
|
作者
Su, Chin-Cheng [1 ,2 ,3 ,4 ]
机构
[1] Changhua Christian Hosp, Tumor Res Ctr Integrat Med, 135 Nan Hsiao St, Changhua 50006, Taiwan
[2] Changhua Christian Hosp, Comprehens Breast Canc Ctr, Changhua 50006, Taiwan
[3] Changhua Christian Hosp, Dept Surg, Changhua 50006, Taiwan
[4] China Med Univ, Sch Chinese Med, Coll Chinese Med, Taichung 40402, Taiwan
关键词
Tanshinone IIA; gastric carcinoma AGS cells; vascular epidermal growth factor receptor; Ras; Raf; MEK; ERK pathway; GROWTH-FACTOR RECEPTOR; CANCER CELLS; BCL-XL; SALVIAE-MILTIORRHIZAE; CASPASE; 12; IN-VITRO; APOPTOSIS; ERK; INDUCTION; MECHANISM;
D O I
10.3892/ijmm.2018.3407
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The RAS/RAF/MEK/ERK pathway is one of the most frequently dysregulated kinase cascades in human cancer, that facilitate the proliferation and survival of cancers driven by growth factor receptors. Tanshinone IIA (Tan-IIA) was extracted from Danshen (Salviae Miltiorrhizae Radix). Tan-IIA inhibition of the proliferation of gastric cancer are well documented, but the molecular mechanisms of Tan-IIA inhibition of gastric cancer have not been well elucidated. We evaluated the protein expression of vascular epidermal growth factor receptor (VEGFR), human epidermal growth factor receptor 2 (HER2), Ras, Raf, MEK, ERK, PARP, caspase-3 and -actin in AGS cells by western blotting. The results showed that AGS cells treated with Tan-IIA upregulated the protein expression of PARP and caspase-3 but decreased VEGFR, HER2, Ras, Raf, MEK and ERK time- and dose-dependently. These findings demonstrated that Tan-IIA inhibited human gastric cancer AGS cells; one of the molecular mechanisms may be through decreasing the protein expression of VEGFR and HER2, then blocking the Ras/Raf/MEK/ERK pathway to induce the activation of PARP and caspase-3 to induce apoptosis.
引用
收藏
页码:2389 / 2396
页数:8
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