Anthocyanin-containing purple-fleshed potatoes suppress colon tumorigenesis via elimination of colon cancer stem cells

被引:97
作者
Charepalli, Venkata [1 ]
Reddivari, Lavanya [2 ]
Radhakrishnan, Sridhar [1 ]
Vadde, Ramakrishna [1 ,3 ]
Agarwal, Rajesh [4 ]
Vanamala, Jairam K. P. [1 ,5 ]
机构
[1] Penn State Univ, Dept Food Sci, University Pk, PA 16802 USA
[2] Penn State Univ, Dept Plant Sci, University Pk, PA 16802 USA
[3] Yogi Vemana Univ, Dept Biotechnol & Bioinformat, Kadapa 516003, AP, India
[4] Univ Colorado, Pharmaceut Sci, Aurora, CO 80045 USA
[5] Penn State Milton S Hershey Med Ctr, Penn State Hershey Canc Inst, Hershey, PA 17033 USA
关键词
Colon cancer stem cells; Purple-fleshed potatoes; Anthocyanins; beta-Catenin; p53; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; WNT/BETA-CATENIN; APOPTOSIS; PROLIFERATION; CHEMOPREVENTION; CARCINOGENESIS; MAINTENANCE; EXPRESSION; GROWTH; TUMORS;
D O I
10.1016/j.jnutbio.2015.08.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cancer stem cells (CSCs) are shown to be responsible for initiation and progression of tumors in a variety of cancers. We previously showed that anthocyanin-containing baked purple-fleshed potato (PP) extracts (PA) suppressed early and advanced human colon cancer cell proliferation and induced apoptosis, but their effect on colon CSCs is not known. Considering the evidence of bioactive compounds, such as anthocyanins, against cancers, there is a critical need to study anticancer activity of PP, a global food crop, against colon CSCs. Thus, isolated colon CSCs (positive for CD44, CD133 and ALDH1b1 markers) with functioning p53 and shRNA-attenuated p53 were treated with PA at 5.0 mu g/ml. Effects of baked PP (20% wt/wt) against colon CSCs were also tested in vivo in mice with azoxymethane-induced colon tumorigenesis. Effects of PA/PP were compared to positive control sulindac. In vitro, PA suppressed proliferation and elevated apoptosis in a p53-independent manner in colon CSCs. PA, but not sulindac, suppressed levels of Wnt pathway effector beta-catenin (a critical regulator of CSC proliferation) and its downstream proteins (c-Myc and cyclin D1) and elevated Bax and cytochrome c, proteins-mediating mitochondrial apoptosis. In vivo, PP reduced the number of crypts containing cells with nuclear beta-catenin (an indicator of colon CSCs) via induction of apoptosis and suppressed tumor incidence similar to that of sulindac. Combined, our data suggest that PP may contribute to reduced colon CSCs number and tumor incidence in vivo via suppression of Wnt/beta-catenin signaling and elevation of mitochondria-mediated apoptosis. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:1641 / 1649
页数:9
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