Aloe-emodin inhibits HER-2 expression through the downregulation of Y-box binding protein-1 in HER-2-overexpressing human breast cancer cells

被引:38
作者
Ma, Jui-Wen [1 ]
Hung, Chao-Ming [2 ,3 ]
Lin, Ying-Chao [4 ,5 ,6 ]
Ho, Chi-Tang [7 ]
Kao, Jung-Yie [1 ]
Way, Tzong-Der [8 ,9 ]
机构
[1] Natl Chung Hsing Univ, Inst Biochem, Coll Life Sci, Taichung, Taiwan
[2] I Shou Univ, E Da Hosp, Dept Gen Surg, Kaohsiung, Taiwan
[3] I Shou Univ, Sch Med, Kaohsiung, Taiwan
[4] Buddhist Tzu Chi Gen Hosp, Taichung Branch, Div Neurosurg, Taichung, Taiwan
[5] Tzu Chi Univ, Sch Med, Hualien, Taiwan
[6] Cent Taiwan Univ Sci & Technol, Dept Med Imaging & Radiol Sci, Taichung, Taiwan
[7] Rutgers State Univ, Dept Food Sci, New Brunswick, NJ USA
[8] China Med Univ, Dept Biol Sci & Technol, Coll Biopharmaceut & Food Sci, Taichung, Taiwan
[9] Asia Univ, Dept Hlth & Nutr Biotechnol, Coll Hlth Sci, Taichung, Taiwan
关键词
HER-2-overexpressing breast cancer cells; aloe-emodin; Y-box binding protein-1; ILK/Akt/mTOR signaling pathway; epithelial-mesenchymal transition; EPITHELIAL-MESENCHYMAL TRANSITION; GROWTH-FACTOR RECEPTOR; LUNG-CANCER; STEM-CELLS; METASTASIS; RESISTANCE; INVASION; TWIST; YB-1; PROLIFERATION;
D O I
10.18632/oncotarget.10410
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Human epidermal growth factor receptor-2 (HER-2)-positive breast cancer tends to be aggressive, highly metastatic, and drug resistant and spreads rapidly. Studies have indicated that emodin inhibits HER-2 expression. This study compared the HER2- inhibitory effects of two compounds extracted from rhubarb roots: aloe-emodin (AE) and rhein. Our results indicated that AE exerted the most potent inhibitory effect on HER-2 expression. Treatment of HER-2-overexpressing breast cancer cells with AE reduced tumor initiation, cell migration, and cell invasion. AE was able to suppress YB-1 expression, further suppressing downstream HER-2 expression. AE suppressed YB-1 expression through the inhibition of Twist in HER-2-overexpressing breast cancer cells. Our data also found that AE inhibited cancer metastasis and cancer stem cells through the inhibition of EMT. Interestingly, AE suppressed YB-1 expression through the downregulation of the intracellular integrin-linked kinase (ILK)/protein kinase B (Akt)/mTOR signaling pathway in HER-2-overexpressing breast cancer cells. In vivo study showed the positive result of antitumor activity of AE in nude mice injected with human HER-2-overexpressing breast cancer cells. These findings suggest the possible application of AE in the treatment of HER-2-positive breast cancer.
引用
收藏
页码:58915 / 58930
页数:16
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