Curcumin-mediated regulation of Notch1/hairy and enhancer of split-1/survivin: molecular targeting in cholangiocarcinoma

被引:24
作者
Koprowski, Steven [1 ]
Sokolowski, Kevin [1 ]
Kunnimalaiyaan, Selvi [1 ]
Gamblin, T. Clark [1 ]
Kunnimalaiyaan, Muthusamy [1 ]
机构
[1] Med Coll Wisconsin, Translat & Biomed Res Ctr, MCW Canc Ctr, Div Surg Oncol,Dept Surg, Milwaukee, WI 53226 USA
关键词
Cholangiocarcinoma; Notch signaling; Survivin; Curcumin; Apoptosis; INTRAHEPATIC CHOLANGIOCARCINOMA; CANCER-CELLS; UNITED-STATES; HILAR CHOLANGIOCARCINOMA; PROGNOSTIC-FACTORS; SURGICAL-TREATMENT; PANCREATIC-CANCER; BILIARY-TRACT; PHASE-I; GROWTH;
D O I
10.1016/j.jss.2015.03.029
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: Cholangiocarcinoma (CCA) is highly malignant and characterized by poor prognosis with chemotherapeutic resistance. Therefore, continued development of novel, effective approaches are needed. Notch expression is markedly upregulated in CCA, but the utility of Notch1 inhibition is not defined. Based on recent findings, we hypothesized that curcumin, a polyphenolic phytochemical, suppresses CCA growth in vitro via inhibition of Notch1 signaling. Methods: Established CCA cell lines CCLP-1 and SG-231 were treated with varying concentrations of curcumin (0-20 mu M). Viability was assessed through 3-(4, 5-dimethylthiazol-2-yl)- 2, 5-diphenyltetrazolium bromide and clonogenic assays. Evaluation of apoptosis was determined via Western analysis for apoptotic markers and Caspase-Glo 3/7 assay. Cell lysates were further analyzed via Western blotting for Notch1/HES-1/survivin pathway expression, cell cycle progression, and survival. Results: Curcumin-treated CCA cells exhibited reduced viability compared with control treatment. Statistically significant reductions in cell viability were observed with curcumin treatment at concentrations of 7.5, 10, and 15 mM by approximately 10%, 48%, and 56% for CCLP-1 and 13%, 25%, and 50% for SG-231, respectively. On Western analysis, concentrations of >= 10 mu M showed reductions in Notch1, HES-1, and survivin. Apoptosis was evidenced by an increase in expression of cleaved poly [ADP] ribose polymerase and an increase in caspase activity. Cyclin D1 (cell cycle progression) expression levels were also reduced with treatment. Conclusions: Curcumin effectively induces CCA (CCLP-1 and SG-231) growth suppression and apoptosis at relatively low treatment concentrations when compared with the previous research. A concomitant reduction of Notch1, HES-1, and survivin expression in CCA cell lines provides novel evidence for a potential antitumorigenic mechanism-of-action. To our knowledge, this is the first report showing reduction in HES-1 expression via protein analysis after treatment with curcumin. Such findings merit further investigation of curcumin-mediated inhibition of Notch signaling in CCA either alone or in combination with chemotherapeutic agents. (C) 2015 Elsevier Inc. All rights reserved.
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收藏
页码:434 / 440
页数:7
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