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

Amira A. Abdellatef, Moustafa Fathy, Abd El Salam I. Mohammed, Marwa S.Abu Bakr, Amal H. Ahmed, Hatem S. Abbass, Ahmed H. El-Desoky, Hiroyuki Morita, Toshio Nikaido, Yoshihiro Hayakawa*

*この論文の責任著者

研究成果: ジャーナルへの寄稿学術論文査読

41 被引用数 (Scopus)

抄録

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.

本文言語英語
ページ(範囲)840-853
ページ数14
ジャーナルNatural Medicines
75
4
DOI
出版ステータス出版済み - 2021/09

ASJC Scopus 主題領域

  • 創薬
  • 補完代替医療
  • 薬科学
  • 有機化学

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