Cryptotanshinone, a Stat3 inhibitor, suppresses colorectal cancer proliferation and growth in vitro

被引:59
|
作者
Li, Weidong [1 ,3 ]
Saud, Shakir M. [2 ,3 ]
Young, Matthew R. [3 ]
Colburn, Nancy H. [3 ]
Hua, Baojin [1 ]
机构
[1] China Acad Chinese Med Sci, Guanganmen Hosp, Dept Oncol, Beijing 100053, Peoples R China
[2] NCI, Nutr Sci Res Grp, Canc Prevent Div, NIH, Rockville, MD 20850 USA
[3] Ctr Canc Res, Basic Res Lab, Frederick Natl Lab Canc Res, Frederick, MD 21702 USA
基金
中国博士后科学基金; 美国国家卫生研究院; 中国国家自然科学基金;
关键词
Cryptotanshinone; Colorectal cancer treatment; Signal transducer and activator of transcription 3; Proliferation; Apoptosis; CELL-PROLIFERATION; COLON-CANCER; CYCLIN D1; SIGNAL TRANSDUCERS; TANSHINONE IIA; POOR-PROGNOSIS; EXPRESSION; APOPTOSIS; CARCINOMA; THERAPY;
D O I
10.1007/s11010-015-2424-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cryptotanshinone (CPT) is a natural compound extracted from herbal medicine that has been previously shown to possess antitumor properties in various types of human cancer cells. In the present study, we examined the potential role of CPT in the treatment of colorectal cancer. Using SW480, HCT116, and LOVO colorectal cancer cell lines, the effects of CPT on cell viability, apoptosis, and tumorigenicity were evaluated. The results showed that CPT significantly inhibited the growth and viability of SW480, HCT116, and LOVO cell lines by inducing apoptosis and prevented anchorage dependent growth on agar. In addition, CPT inhibited the activation of Signal transducer and activator of transcription 3 (Stat3) pathways in colorectal cancer cells. Stat3 is a transcription factor that mediates the expression of various genes associated with many cellular processes, such as inflammation and cell growth, and has been shown to promote several cancer types, including colorectal cancer. These findings indicate that CPT may be a potential candidate for the treatment and prevention of colorectal cancer in part by inhibiting the activation of Stat3.
引用
收藏
页码:63 / 73
页数:11
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