Anticancer properties of chitosan on human melanoma are cell line dependent

被引:81
作者
Gibot, Laure [1 ]
Chabaud, Stephane [1 ]
Bouhout, Sara [1 ]
Bolduc, Stephane [1 ,2 ]
Auger, Francois A. [1 ,2 ]
Moulin, Veronique J. [1 ,2 ]
机构
[1] Univ Laval, Fac Med, Ctr Rech Organogenese Expt, LOEX,Div Regenerat Med,CHU Quebec Res Ctr,FRQS, Quebec City, PQ G1K 7P4, Canada
[2] Univ Laval, Fac Med, Dept Surg, Quebec City, PQ G1K 7P4, Canada
基金
加拿大健康研究院;
关键词
Chitosan; Melanoma; Apoptosis; SULFATED CHITIN DERIVATIVES; IN-VITRO; DRUG-DELIVERY; NANOPARTICLES; DEATH; VIVO; PROLIFERATION; APOPTOSIS; SYSTEM; GROWTH;
D O I
10.1016/j.ijbiomac.2014.08.033
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
Purpose: Chitosan, a natural macromolecule, is widely used in medical and pharmaceutical fields because of its distinctive properties such as bactericide, fungicide and above all its antitumor effects. Although its antitumor activity against different types of cancer had been previously described, its mechanism of action was not fully understood. Materials and methods: Coating of chitosan has been used in cell cultures with A375, SKMEL28, and RPMI7951 cell lines. Adherence, proliferation and apoptosis were investigated. Results: Our results revealed that whereas chitosan decreased adhesion of primary melanoma A375 cell line and decreased proliferation of primary melanoma SKMEL28 cell line, it had potent pro-apoptotic effects against RPMI7951, a metastatic melanoma cell line. In these latter cells, inhibition of specific caspases confirmed that apoptosis was effected through the mitochondrial pathway and Western blot analyses showed that chitosan induced an up regulation of pro-apoptotic molecules such as Bax and a down regulation of anti-apoptotic proteins like Bcl-2 and Bcl-XL. More interestingly, chitosan exposure induced an exposition of a greater number of CD95 receptor at RPMI7951 surface, making them more susceptible to FasL-induced apoptosis. Conclusion: Our results indicate that chitosan could be a promising agent for further evaluations in antitumor treatments targeting melanoma. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:370 / 379
页数:10
相关论文
共 41 条
[1]   Death receptors: Signaling and modulation [J].
Ashkenazi, A ;
Dixit, VM .
SCIENCE, 1998, 281 (5381) :1305-1308
[2]   Oral administration of chitin and chitosan prevents peanut-induced anaphylaxis in a murine food allergy model [J].
Bae, Min-Jung ;
Shin, Hee Soon ;
Kim, En-Kyoung ;
Kim, Jaeheung ;
Shon, Dong-Hwa .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2013, 61 :164-168
[3]   Differential recruitment of caspase 8 to cFlip confers sensitivity or resistance to Fas-mediated apoptosis in a subset of familial lymphoma patients [J].
Bäumler, C ;
Duan, F ;
Onel, K ;
Rapaport, B ;
Jhanwar, S ;
Offit, K ;
Elkon, KB .
LEUKEMIA RESEARCH, 2003, 27 (09) :841-851
[4]   The R1 subunit of herpes simplex virus ribonucleotide reductase has chaperone-like activity similar to Hsp27 [J].
Chabaud, S ;
Lambert, H ;
Sasseville, AMJ ;
Lavoie, H ;
Guilbault, C ;
Massie, B ;
Landry, J ;
Langelier, Y .
FEBS LETTERS, 2003, 545 (2-3) :213-218
[5]   CHITOSAN - AS A BIOMATERIAL [J].
CHANDY, T ;
SHARMA, CP .
BIOMATERIALS ARTIFICIAL CELLS AND ARTIFICIAL ORGANS, 1990, 18 (01) :1-24
[6]  
Dai TH, 2011, EXPERT REV ANTI-INFE, V9, P857, DOI [10.1586/eri.11.59, 10.1586/ERI.11.59]
[7]   Use of a Chitosan-Based Hemostatic Dressing in Dacryocystorhinostomy [J].
Dailey, Roger A. ;
Chavez, Mauricio R. ;
Choi, Dongseok .
OPHTHALMIC PLASTIC AND RECONSTRUCTIVE SURGERY, 2009, 25 (05) :350-353
[8]   Advances in using chitosan-based nanoparticles for in vitro and in vivo drug and gene delivery [J].
Duceppe, Nicolas ;
Tabrizian, Maryam .
EXPERT OPINION ON DRUG DELIVERY, 2010, 7 (10) :1191-1207
[9]   Progress in antimicrobial activities of chitin, chitosan and its oligosaccharides: a systematic study needs for food applications [J].
Dutta, J. ;
Tripathi, S. ;
Dutta, P. K. .
FOOD SCIENCE AND TECHNOLOGY INTERNATIONAL, 2012, 18 (01) :3-34
[10]   Chitosan-based drug nanocarriers: Where do we stand? [J].
Garcia-Fuentes, Marcos ;
Alonso, Maria J. .
JOURNAL OF CONTROLLED RELEASE, 2012, 161 (02) :496-504