Sutherlandia frutescens treatment induces apoptosis and modulates the PI3-kinase pathway in colon cancer cells

被引:12
作者
Leisching, G. [1 ]
Loos, B. [1 ]
Nell, T. [1 ]
Engelbrecht, A. -M. [1 ]
机构
[1] Univ Stellenbosch, Dept Physiol Sci, ZA-7600 Stellenbosch, South Africa
基金
新加坡国家研究基金会;
关键词
Sutherlandia frutescens; Apoptosis; PI3-kinase; CaCo2; cells; PROTEIN-KINASE-B; SIGNALING PATHWAY; STRUCTURAL BASIS; ACTIVATION; BINDING; PHOSPHORYLATION; EXPRESSION; EXTRACTS; SMAC/DIABLO; PROGRESSION;
D O I
10.1016/j.sajb.2015.04.013
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Sutherlandia frutescens is a plant that is endemic to South Africa and is traditionally used for the treatment of cancer and many other ailments. Although previous studies have shown S. frutescens to exert anti-proliferative and apoptotic effects in human mammary adenocarcinoma- and leukemia cell lines, its potential cytotoxic effects on colon cancer cells have not yet been established. Moreover, limited information is available elucidating the major signaling pathways involved upon exposure to the herbal extract. The aim of this study was therefore to assess the cytotoxic effect of S. frutescens on the colon cancer cell line CaCo2, to investigate molecular role players of apoptosis and to assess the involvement of the PI3-K survival pathway. CaCo2 cells exposed to ethanolic extracts of S. frutescens showed significant decreased cell viability, indicated by reduced MTT reductive capacity, increased pyknosis as well as loss in cellular membrane integrity. Western blot analysis revealed a down-regulation in the PI3-K and Akt phosphorylation, a decrease in forkhead transcription factor (FKHR) phosphorylation as well as a concomitant induction of apoptosis. This study demonstrates that Sutherlandia treatment attenuates proliferation of colon cancer cells in vitro by the disruption of the key molecules in the PI-3K( pathway thereby inducing apoptosis. (C) 2015 SAAB. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:20 / 26
页数:7
相关论文
共 41 条
[1]   Mechanism of activation of protein kinase B by insulin and IGF-1 [J].
Alessi, DR ;
Andjelkovic, M ;
Caudwell, B ;
Cron, P ;
Morrice, N ;
Cohen, P ;
Hemmings, BA .
EMBO JOURNAL, 1996, 15 (23) :6541-6551
[2]   Protein kinase B/Akt-mediated phosphorylation promotes nuclear exclusion of the winged helix transcription factor FKHR1 [J].
Biggs, WH ;
Meisenhelder, J ;
Hunter, T ;
Cavenee, WK ;
Arden, KC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (13) :7421-7426
[3]   Akt promotes cell survival by phosphorylating and inhibiting a forkhead transcription factor [J].
Brunet, A ;
Bonni, A ;
Zigmond, MJ ;
Lin, MZ ;
Juo, P ;
Hu, LS ;
Anderson, MJ ;
Arden, KC ;
Blenis, J ;
Greenberg, ME .
CELL, 1999, 96 (06) :857-868
[4]   Anti-diabetic effects of Sutherlandia frutescens in Wistar rats fed a diabetogenic diet [J].
Chadwick, Wayne Anthony ;
Roux, Saartjie ;
de Venter, Maryna van ;
Louw, Johan ;
Oelofsen, Willem .
JOURNAL OF ETHNOPHARMACOLOGY, 2007, 109 (01) :121-127
[5]   Sutherlandia frutescens extracts can induce apoptosis in cultured carcinoma cells [J].
Chinkwo, KA .
JOURNAL OF ETHNOPHARMACOLOGY, 2005, 98 (1-2) :163-170
[6]   The Ganglioside GM3 Is Associated with Cisplatin-Induced Apoptosis in Human Colon Cancer Cells [J].
Chung, Tae-Wook ;
Choi, Hee-Jung ;
Kim, Seok-Jo ;
Kwak, Choong-Hwan ;
Song, Kwon-Ho ;
Jin, Un-Ho ;
Chang, Young-Chae ;
Chang, Hyeun Wook ;
Lee, Young-Choon ;
Ha, Ki-Tae ;
Kim, Cheorl-Ho .
PLOS ONE, 2014, 9 (05)
[7]  
de Almagro M. C., 2012, Experimental Oncology, V34, P200
[8]   Requirement of poly(ADP-ribose) polymerase in recovery from DNA damage in mice and in cells [J].
deMurcia, JM ;
Niedergang, C ;
Trucco, C ;
Ricoul, M ;
Dutrillaux, B ;
Mark, M ;
Oliver, FJ ;
Masson, M ;
Dierich, A ;
LeMeur, M ;
Walztinger, C ;
Chambon, P ;
deMurcia, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (14) :7303-7307
[9]   Smac, a mitochondrial protein that promotes cytochrome c-dependent caspase activation by eliminating IAP inhibition [J].
Du, CY ;
Fang, M ;
Li, YC ;
Li, L ;
Wang, XD .
CELL, 2000, 102 (01) :33-42
[10]  
Filippa N, 1999, MOL CELL BIOL, V19, P4989