scholarly journals Cytotoxicity of snake venom enzymatic toxins: phospholipase A2 and l-amino acid oxidase

2020 ◽  
Vol 48 (2) ◽  
pp. 719-731 ◽  
Author(s):  
Jia Jin Hiu ◽  
Michelle Khai Khun Yap

The phospholipase A2 (PLA2) and l-amino acid oxidase (LAAO) are two major enzymes found in the venoms from most snake species. These enzymes have been structurally and functionally characterised for their pharmacological activities. Both PLA2 and LAAO from different venoms demonstrate considerable cytotoxic effects on cancer cells via induction of apoptosis, cell cycle arrest and suppression of proliferation. These enzymes produce more pronounced cytotoxic effects in cancer cells than normal cells, thus they can be potential sources as chemotherapeutic agents. It is proposed that PLA2 and LAAO contribute to an elevated oxidative stress due to their catalytic actions, for instance, the ability of PLA2 to produce reactive oxygen species during lipolysis and formation of H2O2 from LAAO catalytic activity which consequently lead to cell death. Nonetheless, the cell-death signalling pathways associated with exposure to these enzymatic toxins are not fully elucidated yet. Here in this review, we will discuss the cytotoxic effects of PLA2 and LAAO in relationship to their catalytic mechanisms and the underlying mechanisms of cytotoxic actions.

2021 ◽  
Author(s):  
Li Bo ◽  
Yan Xiong ◽  
Qiyi He ◽  
Xiaodong Yu ◽  
Bo Li ◽  
...  

Abstract The anti-tumor potential of animal toxins has fully attracted the attention of researchers. Snake venoms is a complex mixture of different components and has revealed high toxicity on normal and tumoral tissues or cells. The snake venom L-Amino-acid oxidase (svLAAO) has grown up to be a critical research target in molecular biology sciences and medicine sciences since widespread presence and various biological roles, including antitumor application. We found that Crotalus adamanteus (C. adamanteus) venom LAAO significantly decreased the viability of ovarian cancer cells and caused morphological changes preceded cell death. Cell experiments confirmed that C. adamanteus venom LAAO caused alterations of intrinsic or extrinsic apoptosis pathway-related genes in ovarian cancer cells. Animal experiments and histological analysis also proved that C. adamanteus venom LAAO could effectively inhibit the damage of ovarian cancer to tissues. The major apoptosis induction of C. adamanteus venom LAAO on ovarian cancer cells can be blocked by catalase, suggesting that the cytotoxicity of C. adamanteus venom LAAO on ovarian cancer cells was mainly mediated by H2O2. Our preliminary results revealed that C. adamanteus venom LAAO may induce apoptosis of ovarian cancer cells through the death receptor pathway and mitochondrial pathway. It is inferred that C. adamanteus venom LAAO will be some advantages in New Drug Research and Development of antitumor drugs in the future. Nevertheless, extra studies on the pharmacological actions and molecular mechanism of svLAAO in anti-cancer are necessary in order to better promote its application.


2012 ◽  
Vol 26 (8) ◽  
pp. 308-314 ◽  
Author(s):  
Lucas Benício Campos ◽  
Manuela Berto Pucca ◽  
Eduardo Crosara Roncolato ◽  
Joaquim Coutinho Netto ◽  
José Elpidio Barbosa

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Mauro Valentino Paloschi ◽  
Jéssica Amaral Lopes ◽  
Charles Nunes Boeno ◽  
Milena Daniela Souza Silva ◽  
Jaína Rodrigues Evangelista ◽  
...  

Toxicon ◽  
2010 ◽  
Vol 55 (4) ◽  
pp. 795-804 ◽  
Author(s):  
Alba Fabiola Costa Torres ◽  
Rodrigo Tavares Dantas ◽  
Marcos H. Toyama ◽  
Eduardo Diz Filho ◽  
Fernando José Zara ◽  
...  

RSC Advances ◽  
2017 ◽  
Vol 7 (3) ◽  
pp. 1439-1442 ◽  
Author(s):  
Riccardo Balzaretti ◽  
Fabian Meder ◽  
Marco P. Monopoli ◽  
Luca Boselli ◽  
Ilaria Armenia ◽  
...  

RgDAAO conjugated to γ-Fe2O3NPs generates a low toxic NP-DAAO system, which kills cancer cells through ROS production.


2014 ◽  
Vol 229 ◽  
pp. S100-S101
Author(s):  
Francine Bianchini ◽  
Sandra Burin ◽  
Tassia Costa ◽  
Sandro Ghisla ◽  
Fabiola Castro ◽  
...  

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