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巴西红厚壳素抑制 MDA-MB-231 乳腺癌细胞的迁移和侵袭。

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

机构信息

Department of Medicinal and Applied Chemistry, Kaohsiung Medical University, Kaohsiung 807, Taiwan.

出版信息

Chem Biol Interact. 2013 Jul 5;204(2):105-15. doi: 10.1016/j.cbi.2013.05.005. Epub 2013 May 21.

Abstract

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.

摘要

巴西苏木素是一种从苏木(Caesalpinia sappan L.)中分离得到的生物活性化合物,长期以来一直被用于东方民间药物。癌症转移是癌症死亡的主要原因。然而,巴西苏木素的抗转移作用仍然难以捉摸。在这项研究中,我们发现巴西苏木素通过划痕实验和 Boyden 室分析抑制人乳腺癌 MDA-MB-231 细胞迁移和侵袭。Western blot、明胶酶谱和逆转录-PCR 分析的结果表明,巴西苏木素以浓度依赖性方式抑制基质金属蛋白酶-2(MMP-2)的表达。巴西苏木素还降低了核因子 kappaB(NF-κB)的核蛋白水平。巴西苏木素强烈抑制丝裂原活化蛋白激酶(p38 MAPK)、磷酸肌醇 3-激酶(PI3K)和 Akt 的磷酸化,但不影响细胞外信号调节激酶(ERK1/2)和 c-Jun N-末端激酶(JNK)的磷酸化。此外,用 SB203580(p38 MAPK 抑制剂)或wortmannin(PI3K 抑制剂)处理会导致 MMP-2 的活性和表达降低,以及 MDA-MB-231 细胞迁移和侵袭的抑制。综上所述,这些结果表明,巴西苏木素抑制 MDA-MB-231 细胞可能是通过失活 PI3K/Akt 和 p38 MAPK 信号通路介导的,从而抑制 NF-κB 的激活。因此,巴西苏木素抑制 MMP-2 的表达,从而赋予 MDA-MB-231 细胞抗迁移和抗侵袭能力。

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