Antiproliferative effect of peptide fractions isolated from a quality protein maize, a white hybrid maize, and their derived peptides on hepatocarcinoma human HepG2 cells

被引:46
作者
Ortiz-Martinez, Margarita [1 ,2 ]
de Mejia, Elvira Gonzalez [2 ]
Garcia-Lara, Silverio [1 ]
Aguilar, Oscar [1 ]
Margarita Lopez-Castillo, L. [1 ]
Otero-Pappatheodorou, Jose T. [1 ]
机构
[1] Tecnol Monterrey, Escuela Ingn & Ciencias, Ctr Biotecnol FEMSA, Campus Monterrey,Eugenio Garza Sada 2501, Monterrey 64849, NL, Mexico
[2] Univ Illinois, Dept Food Sci & Human Nutr, Urbana, IL 61801 USA
关键词
Albumins; Antiproliferative; Bioactive peptides; HepG2; Liver cancer; Maize; LUNASIN PROMOTES APOPTOSIS; BEAN PHASEOLUS-VULGARIS; CORN PEPTIDES; GENE-EXPRESSION; NONDIGESTIBLE FRACTION; BIOACTIVE PEPTIDES; POTENTIAL ROLE; LIVER-CANCER; HUMAN COLON; IN-VITRO;
D O I
10.1016/j.jff.2017.04.015
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Hydrolysates and peptides isolated from food proteins have shown antiproliferative effects on cancer cells. Cereals are one of the main sources of protein in the diet; among cereals, maize is the most extensively cultivated and consumed in the world. The aim was to compare the antiproliferative activity of ionic exchange peptide fractions isolated from albumin alcalase hydrolysates of white hybrid (Asgrow-773) and quality protein (CML-502) maize, and their derived peptides, using an in vitro model of human liver cancer. Fraction 10 from Asgrow-773 (IC50 = 8.9 mu g/mL) was more potent (p < 0.05) than the one from CML-502 (IC50 =15.7 mu g/mL). The treatment with fraction 10 from both genotypes increased apoptosis induction rates an average of 4-fold in HepG2 cells. These results suggest that the antiproliferative effect on HepG2 cells of peptide fractions isolated from both genotypes, but not pure peptides, was based on induction of apoptosis due to decrease of antiapoptotic factors expression. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:36 / 48
页数:13
相关论文
共 79 条
[11]  
2-F
[12]   Gene expression signature of human HepG2 cell line [J].
Costantini, S. ;
Di Bernardo, G. ;
Cammarota, M. ;
Castello, G. ;
Colonna, G. .
GENE, 2013, 518 (02) :335-345
[13]   Maximizing recovery of water-soluble proteins through acetone precipitation [J].
Crowell, Andrew M. J. ;
Wall, Mark J. ;
Doucette, Alan A. .
ANALYTICA CHIMICA ACTA, 2013, 796 :48-54
[14]  
Darzynkiewicz Z, 2001, Curr Protoc Cell Biol, VChapter 8, DOI 10.1002/0471143030.cb0804s01
[15]   Flow cytometry in analysis of cell cycle and apoptosis [J].
Darzynkiewicz, Z ;
Bedner, E ;
Smolewski, P .
SEMINARS IN HEMATOLOGY, 2001, 38 (02) :179-193
[16]   Lunasin promotes apoptosis in human colon cancer cells by mitochondrial pathway activation and induction of nuclear clusterin expression [J].
Dia, Vermont P. ;
de Mejia, Elvira Gonzalez .
CANCER LETTERS, 2010, 295 (01) :44-53
[17]   Biologically active peptides derived from egg proteins [J].
Eckert, E. ;
Zambrowicz, A. ;
Pokora, M. ;
Polanowski, A. ;
Chrzanowska, J. ;
Szoltysik, M. ;
Dabrowska, A. ;
Rozanski, H. ;
Trziszka, T. .
WORLDS POULTRY SCIENCE JOURNAL, 2013, 69 (02) :375-386
[18]   Cancer incidence and mortality worldwide: Sources, methods and major patterns in GLOBOCAN 2012 [J].
Ferlay, Jacques ;
Soerjomataram, Isabelle ;
Dikshit, Rajesh ;
Eser, Sultan ;
Mathers, Colin ;
Rebelo, Marise ;
Parkin, Donald Maxwell ;
Forman, David ;
Bray, Freddie .
INTERNATIONAL JOURNAL OF CANCER, 2015, 136 (05) :E359-E386
[19]   Live to die another way: modes of programmed cell death and the signals emanating from dying cells [J].
Fuchs, Yaron ;
Steller, Hermann .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2015, 16 (06) :329-344
[20]   SwissTargetPrediction: a web server for target prediction of bioactive small molecules [J].
Gfeller, David ;
Grosdidier, Aurelien ;
Wirth, Matthias ;
Daina, Antoine ;
Michielin, Olivier ;
Zoete, Vincent .
NUCLEIC ACIDS RESEARCH, 2014, 42 (W1) :W32-W38