Phospholipase A2from kraitBungarus fasciatusvenom induces human cancer cell death in vitro

Author:

Tran Thien V.12,Siniavin Andrei E.3,Hoang Anh N.24,Le My T.T.5,Pham Chuong D.5ORCID,Phung Trung V.6,Nguyen Khoa C.24,Ziganshin Rustam H.7,Tsetlin Victor I.8,Weng Ching-Feng9,Utkin Yuri N.3ORCID

Affiliation:

1. Tra Vinh University, Tra Vinh City, Vietnam

2. Graduate University of Science and Technology VAST, Hanoi, Vietnam

3. Laboratory of Molecular Toxinology, Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry RAS, Moscow, Russian Federation

4. Institute of Applied Materials Science VAST, Ho Chi Minh City, Vietnam

5. Faculty of Applied Sciences, Ton Duc Thang University, Ho Chi Minh City, Vietnam

6. Center for Research and Technology Transfer VAST, Ho Chi Minh City, Vietnam

7. Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry RAS, Moscow, Russian Federation

8. Department of Molecular Neuroimmune Signalling, Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry RAS, Moscow, Russian Federation

9. Department of Life Science and Institute of Biotechnology, National Dong Hwa University, Shoufeng, Hualien, Taiwan

Abstract

BackgroundSnake 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 inBungarus fasciatusvenom an active compound(s) exerting cytotoxic effects toward MCF7 human breast cancer cells and A549 human lung cancer cells.MethodsThe crude venom ofB. fasciatuswas 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.ResultsMTT cell viability assays of cancer cells incubated with fractions isolated fromB. fasciatusvenom 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 A2. 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 A2manifesting the cytotoxicity for cancer cells.

Funder

Vietnam Academy of Science and Technology Research Project

Russian Foundation for Basic Research Project No

Publisher

PeerJ

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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