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Brazilein suppresses migration and invasion of MDA-MB-231 breast cancer cells

机译:Brazilein抑制MDA-MB-231乳腺癌细胞的迁移和侵袭

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Brazilein, a bioactive compound isolated from Caesalpinia sappan L., has long been used in oriental folk medicines. Cancer metastasis is a primary cause of cancer death. However, the anti-metastatic effects of brazilein remain elusive. In this study, we found that brazilein inhibited human breast cancer MDA-MB-231 cell migration and invasion using wound-healing assay and Boyden chamber assay. The results of Western blot, gelatin zymography and reversed transcription-PCR analysis showed that brazilein suppressed matrix metalloproteinase-2 (MMP-2) expression in a concentration-dependent manner. Brazilein also decreased the nuclear protein level of nuclear factor kappaB (NF-κB). Brazilein potently suppressed the phosphorylation of p38 mitogen-activated protein kinase (p38 MAPK), phosphatidylinositide-3-kinase (PI3K) and Akt, but did not affect phosphorylation of extracellular signal regulating kinase (ERK)1/2 and c-Jun N-terminal kinase (JNK). Additionally, treatment of SB203580 (p38 MAPK inhibitor) or wortmannin (PI3K inhibitor) resulted in a reduced activity and expression of MMP-2 as well as inhibition on cell migration and invasion in MDA-MB-231 cells. Taken together, these results suggest that brazilein inhibition of MDA-MB-231 cells may be mediated through inactivation of both PI3K/Akt and p38 MAPK signaling pathways, leading to inhibitory effect on NF-κB activation. Consequently, brazilein suppresses MMP-2 expression, and thus confers anti-migration and anti-invasion of MDA-MB-231 cells.
机译:长期存在于东方民间医学中的巴西青素是一种分离自蓝es(Caesalpinia sappan L.)的生物活性化合物。癌症转移是癌症死亡的主要原因。但是,巴西唑林的抗转移作用仍然难以捉摸。在这项研究中,我们发现使用伤口愈合测定法和博伊登室测定法,巴西来灵抑制人乳腺癌MDA-MB-231细胞的迁移和侵袭。 Western印迹,明胶酶谱和逆转录-PCR分析的结果表明,巴西立素以浓度依赖的方式抑制基质金属蛋白酶2(MMP-2)的表达。巴西橡胶还降低了核因子κB(NF-κB)的核蛋白水平。 Brazilein有效抑制p38丝裂原活化蛋白激酶(p38 MAPK),磷脂酰肌醇-3-激酶(PI3K)和Akt的磷酸化,但不影响细胞外信号调节激酶(ERK)1/2和c-Jun N-的磷酸化。末端激酶(JNK)。此外,SB203580(p38 MAPK抑制剂)或渥曼青霉素(PI3K抑制剂)的处理导致MMP-2的活性和表达降低,并抑制MDA-MB-231细胞中的细胞迁移和侵袭。综上所述,这些结果表明巴西青霉素对MDA-MB-231细胞的抑制作用可能是通过PI3K / Akt和p38 MAPK信号通路的失活来介导的,从而导致对NF-κB活化的抑制作用。因此,巴西来灵抑制MMP-2表达,从而赋予MDA-MB-231细胞抗迁移和抗侵袭性。

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