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从山菅中分离得到的大黄素和大黄酸抑制乳腺癌细胞内固有 NF-κB 活性和转移能力。

Inhibition of cell-intrinsic NF-κB activity and metastatic abilities of breast cancer by aloe-emodin and emodic-acid isolated from Asphodelus microcarpus.

机构信息

Institute of Natural Medicine, University of Toyama, Sugitani 2630, Toyama, 930-0194, Japan.

Department of Regenerative Medicine, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, Japan.

出版信息

J Nat Med. 2021 Sep;75(4):840-853. doi: 10.1007/s11418-021-01526-w. Epub 2021 May 14.

Abstract

Anthraquinones are a major class of compounds naturally occurring in Asphodelus microcarpus. The pharmacological actions of anthraquinones in cancer cells are known to induce apoptosis or autophagy, and revert multidrug resistance. In this study, five anthraquinone-type analogs were isolated from the methanol extract of A. microcarpus leaves and identified as, emodin, rhein, physcion, aloe-emodin, and emodic acid. Among them, aloe-emodin and emodic-acid strongly inhibited the proliferation, cells-intrinsic NF-κB activity and metastatic ability of breast cancer. Although aloe-emodin inhibited p38 and ERK phosphorylation, emodic-acid more markedly inhibited JNK, in addition to p38 and ERK phosphorylation. Both aloe-emodin and emodic-acid inhibited the secretion of the pro-tumorigenic cytokines IL-1β and IL-6, and VEGF and MMP expression, and subsequently inhibited the invasive and migratory potential of 4T1 cells. Thus, our study demonstrated the effects of aloe-emodin and emodin-acid in controlling the migratory and invasive ability of 4T1 breast cancer cells, in addition to inhibiting NF-κB activity and the expression of its downstream target molecules.

摘要

蒽醌类化合物是在 Asphodelus microcarpus 中天然存在的一类主要化合物。已知蒽醌类化合物在癌细胞中的药理作用可诱导细胞凋亡或自噬,并逆转多药耐药性。在这项研究中,从 A. microcarpus 叶甲醇提取物中分离出五种蒽醌类类似物,并鉴定为大黄素、大黄酸、大黄素、芦荟大黄素和大黄酸。其中,芦荟大黄素和大黄酸强烈抑制乳腺癌细胞的增殖、细胞内 NF-κB 活性和转移能力。虽然芦荟大黄素抑制了 p38 和 ERK 的磷酸化,但大黄酸除了抑制 p38 和 ERK 的磷酸化外,还更明显地抑制了 JNK。芦荟大黄素和大黄酸都抑制了促肿瘤细胞因子 IL-1β 和 IL-6 以及 VEGF 和 MMP 的分泌,从而抑制了 4T1 细胞的侵袭和迁移能力。因此,我们的研究表明,芦荟大黄素和大黄酸可通过控制 4T1 乳腺癌细胞的迁移和侵袭能力,除了抑制 NF-κB 活性及其下游靶分子的表达。

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