Efficiency of novel nanocombinations of bovine milk proteins (lactoperoxidase and lactoferrin) for combating different human cancer cell lines

被引:62
作者
Abu-Serie, Marwa M. [1 ]
El-Fakharany, Esmail M. [2 ]
机构
[1] City Sci Res & Technol Applicat SRTA City, Med Biotechnol Dept, Genet Engn & Biotechnol Res Inst, Alexandria 21934, Egypt
[2] City Sci Res & Technol Applicat SRTA City, Prot Res Dept, Genet Engn & Biotechnol Res Inst, Alexandria 21934, Egypt
关键词
CHITOSAN NANOPARTICLES; IDENTIFICATION; INHIBITION; APOPTOSIS; PEPTIDES;
D O I
10.1038/s41598-017-16962-6
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Bovine lactoperoxidase (LPO) and lactoferrin (LF) are suitable proteins to be loaded or adsorbed to chitosan nanoparticles (NPs) for preparing stable nanoformulations with potent anticancer activity. In the present study, nanocombinations of LPO and LF revealed improvement in their stability and activity compared to single (free or nanoformulated) bovine proteins. The coating or loading of LPO-loaded NPs with LF resulted in the highest synergistic cytotoxicity effect against Caco-2, HepG-2, MCF-7 and PC-3 cells in comparison with other NPs and free proteins without causing toxicity toward normal cells. This synergistic improvement in the anticancer activity was apoptosis-dependent that was confirmed by severe alterations in cellular morphology, high percentage of annexin-stained cells and sub-G1 populations as well as nuclear staining with orange fluorescence of treated cancer cells. Additionally, significant alterations in the expression of well characterized cellular proliferation and apoptosis guards (NF-.B, Bcl-2 and p53) in these NPs-treated cancer cells compared to 5-fluorouracil (5-FU) treated cells. Our findings provide for the first time that these new synergistic nanoformulated forms of LPO and LF were superior in their selective apoptosis-mediating anticancer effect than free form of these proteins and 5-FU. LF coating or loading of LPO-loaded NPs present as promising therapy for cancer.
引用
收藏
页数:12
相关论文
共 63 条
[1]   In Vitro Collapsing Colon Cancer Cells by Selectivity of Disulfiram-Loaded Charge Switchable Nanoparticles Against Cancer Stem Cells [J].
Abu-Serie, Marwa M. ;
El-Rashidy, Fatma H. .
RECENT PATENTS ON ANTI-CANCER DRUG DISCOVERY, 2017, 12 (03) :260-271
[2]   Growth inhibition and apoptosis in cancer cells induced by polyphenolic compounds of Acacia hydaspica: Involvement of multiple signal transduction pathways [J].
Afsar, Tayyaba ;
Trembley, Janeen H. ;
Salomon, Christine E. ;
Razak, Suhail ;
Khan, Muhammad Rashid ;
Ahmed, Khalil .
SCIENTIFIC REPORTS, 2016, 6
[3]  
Almahdy O, 2011, HEPAT MON, V11, P724, DOI [10.5812/kowsar.1735143X.722, 10.5812/kowsar.1735143X.1367]
[4]  
Andrade Fernanda, 2011, Curr Drug Discov Technol, V8, P157
[5]   Preparation, characterization, in vitro drug release and biological studies of curcumin loaded dextran sulphate-chitosan nanoparticles [J].
Anitha, A. ;
Deepagan, V. G. ;
Rani, V. V. Divya ;
Menon, Deepthy ;
Nair, S. V. ;
Jayakumar, R. .
CARBOHYDRATE POLYMERS, 2011, 84 (03) :1158-1164
[6]  
Artym J, 2013, POSTEP HIG MED DOSW, V67, P800
[7]   A triterpenoid from wild bitter gourd inhibits breast cancer cells [J].
Bai, Li-Yuan ;
Chiu, Chang-Fang ;
Chu, Po-Chen ;
Lin, Wei-Yu ;
Chiu, Shih-Jiuan ;
Weng, Jing-Ru .
SCIENTIFIC REPORTS, 2016, 6
[8]  
반영은, 2008, [Journal of Cancer Prevention, 대한암예방학회지], V13, P284
[9]   Lactoperoxidase: From catalytic mechanism to practical applications [J].
Boots, J. -W. ;
Floris, Rene .
INTERNATIONAL DAIRY JOURNAL, 2006, 16 (11) :1272-1276
[10]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3