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首页> 外文期刊>Journal of natural medicines >Cannabidiolic acid-mediated selective down-regulation of c-fos in highly aggressive breast cancer MDA-MB-231 cells: possible involvement of its down-regulation in the abrogation of aggressiveness
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Cannabidiolic acid-mediated selective down-regulation of c-fos in highly aggressive breast cancer MDA-MB-231 cells: possible involvement of its down-regulation in the abrogation of aggressiveness

机译:大麻酸介导的C-FOS在高侵袭性乳腺癌MDA-MB-231细胞中的选择性下调:可能涉及其下调在侵略性的废除

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摘要

The physiological activities of cannabidiolic acid (CBDA), a component of fiber-type cannabis plants, have been demonstrated and include its function as a protector against external invasion by inducing cannabinoid-mediated necrosis (Shoyama et al., Plant Signal Behav 3:1111-1112, 2008). The biological activities of CBDA have been attracting increasing attention. We previously identified CBDA as an inhibitor of the migration of MDA-MB-231 cells, a widely used human breast cancer cell line in cancer biology, due to its highly aggressive nature. The chemical inhibition and down-regulation of cyclooxygenase-2 (COX-2), the expression of which has been detected in similar to 40 % of human invasive breast cancers, are suggested to be involved in the CBDA-mediated abrogation of cell migration. However, the molecular mechanism(s) responsible for the CBDA-induced down-regulation of COX-2 in MDA-MB-231 cells have not yet been elucidated. In the present study, we describe a possible mechanism by which CBDA abrogates the expression of COX-2 via the selective down-regulation of c-fos, one component of the activator protein-1 (AP-1) dimer complex, a transcription factor for the positive regulation of the COX-2 gene.
机译:已经证明了大麻酸(CBDA),纤维型大麻植物组分的生理活性,并将其作为保护器通过诱导大麻介导的坏死(Shoyama等,植物信号表现3:1111 -1112,2008)。 CBDA的生物学活性一直在吸引越来越关注。我们之前将CBDA鉴定为MDA-MB-231细胞迁移的抑制剂,由于其高度激进的性质,癌症生物学中广泛使用的人乳腺癌细胞系。环氧氧酶-2(COX-2)的化学抑制和下调,其表达在类似于40%的人类侵袭性乳腺癌中,被提出参与细胞迁移的CBDA介导的。然而,尚未阐明负责CBDA诱导的CBDA-2诱导的CBDA-2的分子机制。在本研究中,我们描述了CBDA通过选择性下调C-FOS,活化剂蛋白-1(AP-1)二聚体复合物,转录因子的一个组分消除了CBDA的一种可能机制。用于COX-2基因的正调节。

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