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熊果酸抑制人肺癌细胞系的增殖、侵袭和迁移。

Inhibition of cell proliferation, invasion and migration by ursolic acid in human lung cancer cell lines.

机构信息

Department of Nutrition, China Medical University, Taichung City, Taiwan, ROC.

出版信息

Toxicol In Vitro. 2011 Oct;25(7):1274-80. doi: 10.1016/j.tiv.2011.04.014. Epub 2011 Apr 20.

Abstract

Ursolic acid (UA) is a pentacyclic triterpene naturally occurring in many plant foods. Apoptotic, anti-invasive and anti-migratory effects of UA at 2, 4, 8, or 16 μmol/L in human non-small cell lung cancer A549, H3255 and Calu-6 cell lines were examined. The impact of this compound upon associated biomarkers such as vascular endothelial growth factor (VEGF), intercellular adhesion molecule-1 (ICAM-1) and matrix metalloproteinase (MMP) was also evaluated. UA treatments concentration-dependently decreased cell viability, and lowered Na(+)-K(+)-ATPase activity (P<0.05). This compound at 4-16 μmol/L concentration-dependently increased DNA fragmentation, and reduced VEGF and transforming growth factor beta1 levels in test cancer cells (P<0.05). UA concentration-dependently suppressed ICAM-1 expression (P<0.05). This compound significantly declined fibronectin expression (P<0.05), but concentration-dependent effect was shown in H3255 cells only (P<0.05). UA treatments significantly suppressed the expression of MMP-9 and MMP-2 (P<0.05), and inhibited protein kinase C activity in test cell lines (P<0.05). UA treatments also concentration-dependently reduced cell invasion (P<0.05); however, this compound at 4-16 μmol/L significantly decreased cell migration (P<0.05), and concentration-dependent effect was shown in A549 and Calu-6 cells (P<0.05). These findings suggested that this triterpene was a potent anti-lung cancer agent, and it might be able to retard invasion and metastasis of lung cancer cells.

摘要

熊果酸(UA)是一种五环三萜,天然存在于许多植物性食物中。在人非小细胞肺癌 A549、H3255 和 Calu-6 细胞系中,研究了 2、4、8 或 16 μmol/L 的 UA 的凋亡、抗侵袭和抗迁移作用。还评估了该化合物对相关生物标志物的影响,如血管内皮生长因子(VEGF)、细胞间黏附分子-1(ICAM-1)和基质金属蛋白酶(MMP)。UA 处理浓度依赖性地降低细胞活力,并降低 Na(+)-K(+)-ATP 酶活性(P<0.05)。该化合物在 4-16 μmol/L 浓度依赖性地增加 DNA 片段化,并降低试验癌细胞中的 VEGF 和转化生长因子β1 水平(P<0.05)。UA 浓度依赖性地抑制 ICAM-1 表达(P<0.05)。该化合物显著降低纤维连接蛋白表达(P<0.05),但仅在 H3255 细胞中显示出浓度依赖性效应(P<0.05)。UA 处理显著抑制 MMP-9 和 MMP-2 的表达(P<0.05),并抑制试验细胞系中的蛋白激酶 C 活性(P<0.05)。UA 处理还浓度依赖性地减少细胞侵袭(P<0.05);然而,该化合物在 4-16 μmol/L 浓度依赖性地显著降低细胞迁移(P<0.05),并在 A549 和 Calu-6 细胞中显示出浓度依赖性效应(P<0.05)。这些发现表明,这种三萜是一种有效的抗肺癌剂,它可能能够延缓肺癌细胞的侵袭和转移。

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