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1.
Int J Biol Macromol ; 103: 25-35, 2017 Oct.
Article in English | MEDLINE | ID: mdl-28495622

ABSTRACT

A new l-amino acid oxidase (LAAO) from Bothrops jararacussu venom (BjussuLAAO-II) was isolated by using a three-step chromatographic procedure based on molecular exclusion, hydrophobicity, and affinity. BjussuLAAO-II is an acidic enzyme with pI=3.9 and molecular mass=60.36kDa that represents 0.3% of the venom proteins and exhibits high enzymatic activity (4884.53U/mg/mim). We determined part of the primary sequence of BjussuLAAO-II by identifying 96 amino acids, from which 34 compose the N-terminal of the enzyme (ADDRNPLEECFRETDYEEFLEIARNGLSDTDNPK). Multiple alignment of the partial BjussuLAAO-II sequence with LAAOs deposited in the NCBI database revealed high similarity (95-97%) with other LAAOs isolated from Bothrops snake venoms. BjussuLAAO-II exerted a strong antiprotozoal effect against Leishmania amazonensis (IC50=4.56µg/mL) and Trypanosoma cruzi (IC50=4.85µg/mL). This toxin also induced cytotoxicity (IC50=1.80µg/mL) and apoptosis in MCF7 cells (a human breast adenocarcinoma cell line) by activating the intrinsic and extrinsic apoptosis pathways, but were not cytotoxic towards MCF10A cells (a non-tumorigenic human breast epithelial cell line). The results reported herein add important knowledge to the field of Toxinology, especially for the development of new therapeutic agents.


Subject(s)
Antiprotozoal Agents/isolation & purification , Antiprotozoal Agents/pharmacology , Apoptosis/drug effects , Bothrops , Crotalid Venoms/enzymology , L-Amino Acid Oxidase/isolation & purification , L-Amino Acid Oxidase/pharmacology , Amino Acid Sequence , Animals , Antiprotozoal Agents/chemistry , Humans , L-Amino Acid Oxidase/chemistry , MCF-7 Cells
2.
Sci Rep ; 7: 42673, 2017 02 16.
Article in English | MEDLINE | ID: mdl-28205610

ABSTRACT

L-amino acid oxidases from snake venoms have been described to possess various biological functions. In this study, we investigated the inflammatory responses induced in vivo and in vitro by CR-LAAO, an L-amino acid oxidase isolated from Calloselasma rhodostoma venom, and its antitumor potential. CR-LAAO induced acute inflammatory responses in vivo, with recruitment of neutrophils and release of IL-6, IL-1ß, LTB4 and PGE2. In vitro, IL-6 and IL-1ß production by peritoneal macrophages stimulated with CR-LAAO was dependent of the activation of the Toll-like receptors TLR2 and TLR4. In addition, CR-LAAO promoted apoptosis of HL-60 and HepG2 tumor cells mediated by the release of hydrogen peroxide and activation of immune cells, resulting in oxidative stress and production of IL-6 and IL-1ß that triggered a series of events, such as activation of caspase 8, 9 and 3, and the expression of the pro-apoptotic gene BAX. We also observed that CR-LAAO modulated the cell cycle of these tumor cells, promoting delay in the G0/G1 and S phases. Taken together, our results suggest that CR-LAAO could serve as a potential tool for the development of novel immunotherapeutic strategies against cancer, since this toxin promoted apoptosis of tumor cells and also activated immune cells against them.


Subject(s)
L-Amino Acid Oxidase/metabolism , Snake Venoms/enzymology , Viperidae/metabolism , Animals , Apoptosis/drug effects , Apoptosis/genetics , Caspases/metabolism , Cell Cycle/drug effects , Cell Cycle/genetics , Cell Line, Tumor , Cytokines/metabolism , Humans , Immunotherapy , Inflammation Mediators/metabolism , L-Amino Acid Oxidase/immunology , L-Amino Acid Oxidase/pharmacology , L-Amino Acid Oxidase/therapeutic use , Neoplasms/immunology , Neoplasms/metabolism , Neoplasms/therapy , Neutrophil Infiltration , Neutrophils/immunology , Neutrophils/metabolism , Neutrophils/pathology , Oxidative Stress/drug effects , Signal Transduction/drug effects , Snake Venoms/immunology , Snake Venoms/pharmacology , Snake Venoms/therapeutic use , Toll-Like Receptor 2/metabolism , Toll-Like Receptor 4/metabolism
3.
J. venom. anim. toxins incl. trop. dis ; 20: 1-7, 04/02/2014. tab, ilus
Article in English | LILACS, VETINDEX | ID: biblio-1484558

ABSTRACT

The L-amino acid oxidases (LAAOs) constitute a major component of snake venoms and have been widely studied due to their widespread presence and various effects, such as apoptosis induction, cytotoxicity, induction and/or inhibition of platelet aggregation, hemorrhage, hemolysis, edema, as well as antimicrobial, antiparasitic and anti-HIV activities. The isolated and characterized snake venom LAAOs have become important research targets due to their potential biotechnological applications in pursuit for new drugs of interest in the scientific and medical fields. The current study discusses the antitumor effects of snake venom LAAOs described in the literature to date, highlighting the mechanisms of apoptosis induction proposed for this class of proteins.


Subject(s)
Animals , L-Amino Acid Oxidase/analysis , Oxidoreductases/analysis , Poisons/administration & dosage , Snakes/classification
4.
Article in English | LILACS | ID: lil-724668

ABSTRACT

The L-amino acid oxidases (LAAOs) constitute a major component of snake venoms and have been widely studied due to their widespread presence and various effects, such as apoptosis induction, cytotoxicity, induction and/or inhibition of platelet aggregation, hemorrhage, hemolysis, edema, as well as antimicrobial, antiparasitic and anti-HIV activities. The isolated and characterized snake venom LAAOs have become important research targets due to their potential biotechnological applications in pursuit for new drugs of interest in the scientific and medical fields. The current study discusses the antitumor effects of snake venom LAAOs described in the literature to date, highlighting the mechanisms of apoptosis induction proposed for this class of proteins.


Subject(s)
Animals , L-Amino Acid Oxidase/analysis , Oxidoreductases/analysis , Poisons/administration & dosage , Snakes/classification
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