Antifungal and antitumor models of bioactive protective peptides

被引:34
作者
Rodrigues, Elaine G. [1 ]
Dobroff, Andrey S. [1 ]
Taborda, Carlos P. [2 ]
Travassos, Luiz R. [1 ]
机构
[1] Univ Fed Sao Paulo, Unidade Oncol Expt, Dept Microbiol Imunol & Parasitol, BR-04023062 Sao Paulo, Brazil
[2] Univ Sao Paulo, Dept Microbiol, Inst Ciencias Biomed, BR-05508900 Sao Paulo, Brazil
来源
ANAIS DA ACADEMIA BRASILEIRA DE CIENCIAS | 2009年 / 81卷 / 03期
基金
巴西圣保罗研究基金会;
关键词
bioactive peptides; Paracoccidioides brasiliensis; tumor cells; killer peptide; melanoma; apoptosis; MAJOR DIAGNOSTIC ANTIGEN; SPIDER ACANTHOSCURRIA-GOMESIANA; CELLS IN-VITRO; ANTIMICROBIAL PEPTIDE; PARACOCCIDIOIDES-BRASILIENSIS; KILLER TOXIN; THERAPEUTIC ACTIVITY; MONOCLONAL-ANTIBODY; PSEUDOMONAS-CEPACIA; ANTICANCER ACTIVITY;
D O I
10.1590/S0001-37652009000300015
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
Peptides are remarkably reactive molecules produced by a great variety of species and able to display a number of functions in uni- and multicellular organisms as mediators, agonists and regulating substances. Some of them exert cytotoxic effects on cells other than those that produced them, and may have a role in controlling subpopulations and protecting certain species or cell types. Presently, we focus on antifungal and antitumor peptides and discuss a few models in which specific sequences and structures exerted direct inhibitory effects or stimulated a protective immune response. The killer peptide, deduced from an antiidiotypic antibody, with several antimicrobial activities and other Ig-derived peptides with cytotoxic activities including antitumor effects, are models studied in vitro and in vivo. Peptide 10 from gp43 of P. brasiliensis (P10) and the vaccine perspective against paracoccidioidomycosis is another topic illustrating the protective effect in vivo against a pathogenic fungus. The cationic antimicrobial peptides with antitumor activities are mostly reviewed here. Local treatment of murine melanoma by the peptide gomesin is another model studied at the Experimental Oncology Unit of UNIFESP.
引用
收藏
页码:503 / 520
页数:18
相关论文
共 139 条
  • [1] The mode of antifungal action of plant, insect and human defensins
    Aerts, A. M.
    Francois, I. E. J. A.
    Cammue, B. P. A.
    Thevissen, K.
    [J]. CELLULAR AND MOLECULAR LIFE SCIENCES, 2008, 65 (13) : 2069 - 2079
  • [2] Gomesin, a peptide produced by the spider Acanthoscurria gomesiana, is a potent anticryptococcal agent that acts in synergism with fluconazole
    Barbosa, Fabiane M.
    Daffre, Sirlei
    Maldonado, Rosa A.
    Miranda, Antonio
    Nimrichter, Leonardo
    Rodrigues, Marcio L.
    [J]. FEMS MICROBIOLOGY LETTERS, 2007, 274 (02) : 279 - 286
  • [3] Structure and functions of channel-forming peptides: Magainins, cecropins, melittin and alamethicin
    Bechinger, B
    [J]. JOURNAL OF MEMBRANE BIOLOGY, 1997, 156 (03) : 197 - 211
  • [4] Prophylactic administration of a complementarity-determining region derived from a neutralizing monoclonal antibody is effective against respiratory syncytial virus infection in BALB/c mice
    Bourgeois, C
    Bour, JB
    Aho, LS
    Pothier, P
    [J]. JOURNAL OF VIROLOGY, 1998, 72 (01) : 807 - 810
  • [5] Systemic fungal infections caused by Aspergillus species:: Epidemiology, infection process and virulence determinants
    Brakhage, AA
    [J]. CURRENT DRUG TARGETS, 2005, 6 (08) : 875 - 886
  • [6] The monoclonal antibody against the major diagnostic antigen of Paracoccidioides brasiliensis mediates immune protection in infected BALB/c mice challenged intratracheally with the fungus
    Buissa-Filho, R.
    Puccia, R.
    Marques, A. F.
    Pinto, F. A.
    Munoz, J. E.
    Nosanchuk, J. D.
    Travassos, L. R.
    Taborda, C. P.
    [J]. INFECTION AND IMMUNITY, 2008, 76 (07) : 3321 - 3328
  • [7] Buzaid AC, 2001, CLIN CANCER RES, V7, P2611
  • [8] A synthetic peptide as a novel anticryptococcal agent
    Cenci, E
    Bistoni, F
    Mencacci, A
    Perito, S
    Magliani, W
    Conti, S
    Polonelli, L
    Vecchiarelli, A
    [J]. CELLULAR MICROBIOLOGY, 2004, 6 (10) : 953 - 961
  • [9] Chan SC, 1998, J PEPT SCI, V4, P413, DOI 10.1002/(SICI)1099-1387(199811)4:7<413::AID-PSC160>3.0.CO
  • [10] 2-W