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      Cytotoxic and anticancer properties of the Malaysian mangrove pit viper ( Trimeresurus purpureomaculatus) venom and its disintegrin (purpureomaculin)

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          Abstract

          Background:

          The Asiatic pit vipers from the Trimeresurus complex are medically important venomous snakes. These pit vipers are often associated with snakebite that leads to fatal coagulopathy and tissue necrosis. The cytotoxic venoms of Trimeresurus spp.; however, hold great potential for the development of peptide-based anticancer drugs.

          Methods:

          This study investigated the cytotoxic effect of the venom from Trimeresurus purpureomaculatus, the mangrove pit viper (also known as shore pit viper) which is native in Malaysia, across a panel of human cancer cell lines from breast, lung, colon and prostate as well as the corresponding normal cell lines of each tissue.

          Results:

          The venom exhibited dose-dependent cytotoxic activities on all cell lines tested, with median inhibition concentrations (IC 50) ranging from 0.42 to 6.98 µg/mL. The venom has a high selectivity index (SI = 14.54) on breast cancer cell line (MCF7), indicating that it is significantly more cytotoxic toward the cancer than to normal cell lines. Furthermore, the venom was fractionated using C 18 reversed-phase high-performance liquid chromatography and the anticancer effect of each protein fraction was examined. Fraction 1 that contains a hydrophilic low molecular weight (approximately 7.5 kDa) protein was found to be the most cytotoxic and selective toward the breast cancer cell line (MCF7). The protein was identified using liquid chromatography-tandem mass spectrometry as a venom disintegrin, termed purpureomaculin in this study.

          Conclusion:

          Taken together, the findings revealed the potent and selective cytotoxicity of a disintegrin protein isolated from the Malaysian T. purpureomaculatus venom and suggested its anticancer potential in drug discovery.

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          Most cited references51

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          Complex cocktails: the evolutionary novelty of venoms.

          Venoms have evolved on numerous occasions throughout the animal kingdom. These 'biochemical weapon systems' typically function to facilitate, or protect the producing animal from, predation. Most venomous animals remain unstudied despite venoms providing model systems for investigating predator-prey interactions, molecular evolution, functional convergence, and novel targets for pharmaceutical discovery. Through advances in 'omic' technologies, venom composition data have recently become available for several venomous lineages, revealing considerable complexity in the processes responsible for generating the genetic and functional diversity observed in many venoms. Here, we review these recent advances and highlight the ecological and evolutionary novelty of venom systems. Copyright © 2012 Elsevier Ltd. All rights reserved.
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            Correlation between stability of a protein and its dipeptide composition: a novel approach for predicting in vivo stability of a protein from its primary sequence

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              The use of therapeutic peptides to target and to kill cancer cells.

              Peptide therapeutics is a promising field for emerging anti-cancer agents. Benefits include the ease and rapid synthesis of peptides and capacity for modifications. An existing and vast knowledge base of protein structure and function can be exploited for novel peptide design. Current research focuses on developing peptides that can (1) serve as tumor targeting moieties and (2) permeabilize membranes with cytotoxic consequences. A survey of recent findings reveals significant trends. Amphiphilic peptides with clusters of hydrophobic and cationic residues are features of anti-microbial peptides that confer the ability to eradicate microbes and show considerable anti-cancer toxicity. Peptides that assemble and form pores can disrupt cell or organelle membranes and cause apoptotic or necrotic death. Cell permeable and tumor-homing peptides can carry biologically active cargo to tumors or tumor vasculature. The challenge lies in developing the clinical application of therapeutic peptides. Improving delivery to tumors, minimizing non-specific toxic effects and discerning pharmacokinetic properties are high among the needs to produce a powerful therapeutic peptide for cancer treatment.
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                Author and article information

                Journal
                J Venom Anim Toxins Incl Trop Dis
                J Venom Anim Toxins Incl Trop Dis
                jvatitd
                The Journal of Venomous Animals and Toxins Including Tropical Diseases
                Centro de Estudos de Venenos e Animais Peçonhentos
                1678-9199
                17 July 2020
                2020
                : 26
                : e20200013
                Affiliations
                [1 ]Department of Pharmacology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
                [2 ]Institute of Biological Sciences, Faculty of Science, University of Malaya, Kuala Lumpur, Malaysia.
                [3 ]Department of Molecular Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
                Author notes
                [* ] Correspondence: tanch@ 123456um.edu.my

                Competing interests: The authors declare no conflict of interest.

                Authors’ Contributions: CHT and KYT conceived the study and designed experiments. NHT, KSS and SN participated in the study design and methodology. CHT, KYT and KSS provided resources. JLL performed experiments and analysis of data. CHT, KYT and JLL interpreted and curated the data. CHT and JLL wrote the main article. All authors read, revised and approved the final manuscript.

                Author information
                http://orcid.org/0000-0003-1416-077X
                Article
                00320
                10.1590/1678-9199-JVATITD-2020-0013
                7375409
                32742279
                66116556-5ec9-424e-bc90-26400f807a4a

                This article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/ ), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/ ) applies to the data made available in this article, unless otherwise stated.

                History
                : 04 February 2020
                : 29 May 2020
                Page count
                Figures: 6, Tables: 3, Equations: 2, References: 55
                Categories
                Research

                shore pit viper,trimeresurus purpureomaculatus,disintegrin,selective cytotoxicity,anti-neoplastic activity

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