Phospholipase A2 from krait Bungarus fasciatus venom induces human cancer cell death in vitro

被引:17
作者
Tran, Thien V. [1 ,2 ]
Siniavin, Andrei E. [3 ]
Hoang, Anh N. [2 ,4 ]
Le, My T. T. [5 ]
Pham, Chuong D. [5 ]
Phung, Trung V. [6 ]
Nguyen, Khoa C. [2 ,4 ]
Ziganshin, Rustam H. [7 ]
Tsetlin, Victor I. [8 ]
Weng, Ching-Feng [9 ]
Utkin, Yuri N. [3 ]
机构
[1] Tra Vinh Univ, Tra Vinh City, Vietnam
[2] Grad Univ Sci & Technol VAST, Hanoi, Vietnam
[3] RAS, Shemyakin Ovchinnikov Inst Bioorgan Chem, Lab Mol Toxinol, Moscow, Russia
[4] Inst Appl Mat Sci VAST, Ho Chi Minh City, Vietnam
[5] Ton Duc Thang Univ, Fac Sci Appl, Ho Chi Minh City, Vietnam
[6] Ctr Res & Technol Transfer VAST, Ho Chi Minh City, Vietnam
[7] RAS, Shemyakin Ovchinnikov Inst Bioorgan Chem, Moscow, Russia
[8] RAS, Shemyakin Ovchinnikov Inst Bioorgan Chem, Dept Mol Neuroimmune Signalling, Moscow, Russia
[9] Natl Dong Hwa Univ, Dept Life Sci & Inst Biotechnol, Hualien, Taiwan
来源
PEERJ | 2019年 / 7卷
基金
俄罗斯基础研究基金会;
关键词
Phospholipase A2; Venom; Krait; Cytotoxicity; Human cancer cells; Breast cancer; Lung cancer; Mass spectrometry; AMINO-ACID OXIDASE; C-TERMINAL REGION; SNAKE-VENOM; COBRA VENOM; ANTIPROLIFERATIVE ACTIVITY; PEPTIDES; PURIFICATION; APOPTOSIS; PROLIFERATION; MULTICINCTUS;
D O I
10.7717/peerj.8055
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
Background: Snake venoms are the complex mixtures of different compounds manifesting a wide array of biological activities. The venoms of kraits (genus Bungarus, family Elapidae) induce mainly neurological symptoms; however, these venoms show a cytotoxicity against cancer cells as well. This study was conducted to identify in Bungarus fasciatus venom an active compound(s) exerting cytotoxic effects toward MCF7 human breast cancer cells and A549 human lung cancer cells. Methods: The crude venom of B. fasciatus was separated by gel-filtration on Superdex HR 75 column and reversed phase HPLC on C18 column. The fractions obtained were screened for cytotoxic effect against MCF7, A549, and HK2 cell lines using colorimetric assay with the tetrazolium dye MTT- 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide. The primary structure of active protein was established by ultra high resolution LC-MS/MS. The molecular mechanism of the isolated protein action on MCF7 cells was elucidated by flow cytometry. Results: MTT cell viability assays of cancer cells incubated with fractions isolated from B. fasciatus venom revealed a protein with molecular mass of about 13 kDa possessing significant cytotoxicity. This protein manifested the dose and time dependent cytotoxicity for MCF7 and A549 cell lines while showed no toxic effect on human normal kidney HK2 cells. In MCF7, flow cytometry analysis revealed a decrease in the proportion of Ki-67 positive cells. As Ki-67 protein is a cellular marker for proliferation, its decline indicates the reduction in the proliferation of MCF7 cells treated with the protein. Flow cytometry analysis of MCF7 cells stained with propidium iodide and Annexin V conjugated with allophycocyanin showed that a probable mechanism of cell death is apoptosis. Mass spectrometric studies showed that the cytotoxic protein was phospholipase A(2). The amino acid sequence of this enzyme earlier was deduced from cloned cDNA, and in this work it was isolated from the venom as a protein for the first time. It is also the first krait phospholipase A(2) manifesting the cytotoxicity for cancer cells.
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页数:22
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