Silibinin suppresses bladder cancer through down-regulation of actin cytoskeleton and PI3K/Akt signaling pathways

被引:46
作者
Imai-Sumida, Mitsuho [1 ,2 ]
Chiyomaru, Takeshi [1 ,2 ,3 ]
Majid, Shahana [1 ,2 ]
Saini, Sharanjot [1 ,2 ]
Nip, Hannah [1 ,2 ]
Dahiya, Rajvir [1 ,2 ]
Tanaka, Yuichiro [1 ,2 ]
Yamamura, Soichiro [1 ,2 ]
机构
[1] San Francisco VA Med Ctr, Dept Urol, San Francisco, CA 94121 USA
[2] Univ Calif San Francisco, San Francisco, CA 94143 USA
[3] Natl Hosp Org, Kagoshima Med Ctr, Dept Urol, Kagoshima, Japan
基金
美国国家卫生研究院;
关键词
silibinin; bladder cancer; KRAS; PI3K; long non-coding RNA; NONCODING RNA HOTAIR; BREAST-CANCER; CARCINOMA PROGRESSION; GROWTH-FACTOR; LONG; APOPTOSIS; ACTIVATION; EXPRESSION; INDUCTION; PROSTATE;
D O I
10.18632/oncotarget.20734
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Silibinin is the major active constituent of silymarin, an extract of milk thistle seeds. Silibinin has been shown to have significant anti-cancer effects in a variety of malignancies. However, the molecular mechanisms of silibinin action in bladder cancer have not been studied extensively. In the present study, we found that silibinin (10 mu M) significantly suppressed proliferation, migration, invasion and induced apoptosis of T24 and UM-UC-3 human bladder cancer cells. Silibinin down-regulated the actin cytoskeleton and phosphatidylinositide 3-kinase (PI3K)/Akt signaling pathways in these cancer cell lines. These pathways were found to crosstalk through RAS cascades. We found that silibinin suppressed levels of trimethylated histone H3 lysine 4 and acetylated H3 at the KRAS promoter. Furthermore, silibinin targets long non-coding RNA: HOTAIR and ZFAS1, which are known to play roles as oncogenic factors in various cancers. This study shows that silibinin exerts anti-cancer effects through down-regulation of actin cytoskeleton and PI3K/Akt pathways and thus suppresses bladder cancer growth and progression.
引用
收藏
页码:92032 / 92042
页数:11
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